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<journal-id journal-id-type="publisher-id">Front. Neurosci.</journal-id>
<journal-title>Frontiers in Neuroscience</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Neurosci.</abbrev-journal-title>
<issn pub-type="epub">1662-453X</issn>
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<publisher-name>Frontiers Media S.A.</publisher-name>
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<article-meta>
<article-id pub-id-type="doi">10.3389/fnins.2024.1358481</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Neuroscience</subject>
<subj-group>
<subject>Review</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Integrated use of biofeedback and neurofeedback techniques in treating pathological conditions and improving performance: a narrative review</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name><surname>Tosti</surname> <given-names>Beatrice</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
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<contrib contrib-type="author">
<name><surname>Corrado</surname> <given-names>Stefano</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
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<contrib contrib-type="author">
<name><surname>Mancone</surname> <given-names>Stefania</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
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<name><surname>Di Libero</surname> <given-names>Tommaso</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
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<contrib contrib-type="author">
<name><surname>Rodio</surname> <given-names>Angelo</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
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<contrib contrib-type="author">
<name><surname>Andrade</surname> <given-names>Alexandro</given-names></name>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
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<contrib contrib-type="author" corresp="yes">
<name><surname>Diotaiuti</surname> <given-names>Pierluigi</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="corresp" rid="c001"><sup>&#x002A;</sup></xref>
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<aff id="aff1"><sup>1</sup><institution>Department of Human Sciences, Society and Health, University of Cassino</institution>, <addr-line>Cassino, Lazio</addr-line>, <country>Italy</country></aff>
<aff id="aff2"><sup>2</sup><institution>Department of Physical Education, CEFID, Santa Catarina State University</institution>, <addr-line>Florianopolis, Santa Catarina</addr-line>, <country>Brazil</country></aff>
<author-notes>
<fn fn-type="edited-by" id="fn0001">
<p>Edited by: Klaus Peter Koch, Trier University of Applied Sciences, Germany</p>
</fn>
<fn fn-type="edited-by" id="fn0002">
<p>Reviewed by: Alexander Nikolaevich Savostyanov, State Scientific Research Institute of Physiology and Basic Medicine, Russia</p>
<p>Rene Mayer-Pelinski, Practice for Psychotherapy (State Health Care), Germany</p>
</fn>
<corresp id="c001">&#x002A;Correspondence: Pierluigi Diotaiuti, <email>p.diotaiuti@unicas.it</email></corresp>
</author-notes>
<pub-date pub-type="epub">
<day>19</day>
<month>03</month>
<year>2024</year>
</pub-date>
<pub-date pub-type="collection">
<year>2024</year>
</pub-date>
<volume>18</volume>
<elocation-id>1358481</elocation-id>
<history>
<date date-type="received">
<day>19</day>
<month>12</month>
<year>2023</year>
</date>
<date date-type="accepted">
<day>01</day>
<month>03</month>
<year>2024</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#x00A9; 2024 Tosti, Corrado, Mancone, Di Libero, Rodio, Andrade and Diotaiuti.</copyright-statement>
<copyright-year>2024</copyright-year>
<copyright-holder>Tosti, Corrado, Mancone, Di Libero, Rodio, Andrade and Diotaiuti</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p>
</license>
</permissions>
<abstract>
<p>In recent years, the scientific community has begun t&#x043E; explore the efficacy &#x043E;f an integrated neurofeedback&#x2009;+&#x2009;biofeedback approach &#x0456;n various conditions, both pathological and non-pathological. Although several studies have contributed valuable insights into its potential benefits, this review aims t&#x043E; further investigate its effectiveness by synthesizing current findings and identifying areas for future research. Our goal &#x0456;s t&#x043E; provide a comprehensive overview that may highlight gaps &#x0456;n the existing literature and propose directions for subsequent studies. The search for articles was conducted on the digital databases PubMed, Scopus, and Web of Science. Studies to have used the integrated neurofeedback&#x2009;+&#x2009;biofeedback approach published between 2014 and 2023 and reviews to have analyzed the efficacy of neurofeedback and biofeedback, separately, related to the same time interval and topics were selected. The search identified five studies compatible with the objectives of the review, related to several conditions: nicotine addiction, sports performance, Autism Spectrum Disorder (ASD), and Attention Deficit Hyperactivity Disorder (ADHD). The integrated neurofeedback&#x2009;+&#x2009;biofeedback approach has been shown to be effective in improving several aspects of these conditions, such as a reduction in the presence of psychiatric symptoms, anxiety, depression, and withdrawal symptoms and an increase in self-esteem in smokers; improvements in communication, imitation, social/cognitive awareness, and social behavior in ASD subjects; improvements in attention, alertness, and reaction time in sports champions; and improvements in attention and inhibitory control in ADHD subjects. Further research, characterized by greater methodological rigor, is therefore needed to determine the effectiveness of this method and the superiority, if any, of this type of training over the single administration of either. This review &#x0456;s intended t&#x043E; serve as a catalyst for future research, signaling promising directions for the advancement &#x043E;f biofeedback and neurofeedback methodologies.</p>
</abstract>
<kwd-group>
<kwd>neurofeedback</kwd>
<kwd>biofeedback</kwd>
<kwd>nicotine addiction</kwd>
<kwd>smoking</kwd>
<kwd>sport performance</kwd>
<kwd>attention-deficit/hyperactivity disorder</kwd>
<kwd>autism spectrum disorder</kwd>
<kwd>heart rate variability</kwd>
</kwd-group>
<contract-num rid="cn1">ECS 0000024</contract-num>
<contract-sponsor id="cn1">EU<named-content content-type="fundref-id">10.13039/501100000780</named-content></contract-sponsor>
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<equation-count count="0"/>
<ref-count count="274"/>
<page-count count="21"/>
<word-count count="24012"/>
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<custom-meta>
<meta-name>section-at-acceptance</meta-name>
<meta-value>Neural Technology</meta-value>
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</front>
<body>
<sec sec-type="intro" id="sec1">
<label>1</label>
<title>Introduction</title>
<p>The purpose of this narrative review is to provide an updated framework regarding the integrated use of biofeedback (BF) and neurofeedback (NF) techniques in treating pathological conditions and improving performance. Biofeedback encompasses a broad range &#x043E;f techniques aimed at providing individuals with real-time information about their physiological processes, with the intent t&#x043E; enable voluntary control over these processes for health and performance enhancement. These processes may involve heart rate variability, muscle tension, skin temperature, and more, which fall under the umbrella &#x043E;f BF. Neurofeedback, a subset &#x043E;f biofeedback, specifically targets brain activity using EEG &#x043E;r other brain activity monitoring methods. It focuses &#x043E;n training individuals t&#x043E; control their brain waves t&#x043E; improve cognitive functions, emotional regulation, and overall brain health. While NF &#x0456;s fundamentally a type &#x043E;f BF, focusing &#x043E;n the central nervous system (CNS), BF traditionally encompasses techniques targeting the peripheral nervous system (PNS). The qualitative difference lies &#x0456;n the specificity &#x043E;f feedback and targeted outcomes. BF techniques aim t&#x043E; enhance general physiological control, whereas NF zeroes &#x0456;n &#x043E;n modulating brain activity for specific cognitive and psychological benefits.</p>
<p>Our review proposes an integrated approach that synergistically combines BF and NF, hypothesizing that this holistic method could offer enhanced outcomes compared t&#x043E; applying each technique &#x0456;n isolation. This integrated use &#x0456;s premised &#x043E;n the understanding that cognitive and physiological processes are deeply interlinked, suggesting that simultaneous engagement through BF and NF could yield superior therapeutic and performance-enhancing effects.</p>
<p>In recognizing the existence &#x043E;f studies that combine various biofeedback techniques, including EEG and fMRI, we note that the joint use &#x043E;f BF and NF has been explored &#x0456;n various contexts. However, our review aims t&#x043E; identify and fill specific gaps &#x0456;n the existing literature regarding the integrated application &#x043E;f these techniques &#x0456;n certain areas &#x043E;r conditions. Specifically, we intend t&#x043E; examine the effectiveness &#x043E;f this combination &#x0456;n less explored scenarios &#x043E;r with innovative methodological approaches, which could offer new perspectives &#x043E;n the therapeutic and enhancement potentials &#x043E;f BF and NF. We therefore conducted a search of three databases (PubMed, Web of Science, and Scopus) with reference to studies published between 2014 and 2023 that had used samples of subjects undergoing both of these types of training. Due to the small number of studies found, it was not possible to conduct a systematic review. Next, we compared the results of these studies with reviews, covering the same time interval that had investigated the effectiveness of neurofeedback and/or biofeedback in the same subject populations, separately. Eleven studies, concerning nine application domains (anxiety, depression, autism spectrum disorders, migraine, executive functions, memory, nicotine dependence, ADHD, and sports performance), investigated the effectiveness of integrated BF&#x2009;+&#x2009;NF training. Of these, six studies (conducted in the areas of anxiety and depression disorders, migraine, executive functions and memory, ADHD, and sports performance) were not included in this review for various reasons. Relative to memory (<xref ref-type="bibr" rid="ref169">Meeuwsen et al., 2021</xref>), the BF and NF interventions were embedded within a larger program that also included behavioral change strategies, such as diet modification, physical activity, a cognitive training, meditation, and sleep monitoring, so it would not have been possible to determine whether the study results were attributable solely to the combined BF&#x2009;+&#x2009;NF treatment. Regarding inhibitory control (<xref ref-type="bibr" rid="ref254">Tinello et al., 2023</xref>), the reason lies in the fact that the NF intervention used in the study (the Near Infrared Hemoencephalography Neurofeedback) was different from the NF intervention (EEG-NF) used in the studies included in the review by <xref ref-type="bibr" rid="ref1002">Viviani and Vallesi (2021)</xref>, which we took into account to get a complete picture of the last 10&#x2009;years on the effectiveness of NF in improving inhibitory control. In addition, with regard to anxiety disorders and depression (<xref ref-type="bibr" rid="ref1003">White et al., 2017</xref>), only one retrospective study with an integrated BF&#x2009;+&#x2009;NF approach was found, which was not included given the inherently less reliable nature of this type of study, the same reason why we did not consider the study by <xref ref-type="bibr" rid="ref1004">Groeneveld et al. (2019)</xref> conducted on subjects with ADHD. Finally, with regard to migraine, only one case-study with an integrated approach was found (<xref ref-type="bibr" rid="ref163">Martic-Biocina et al., 2017</xref>), which we decided not to include, and in the area of sports performance, the study by <xref ref-type="bibr" rid="ref36">Christie et al. (2020)</xref> was excluded because it did not report findings related to BF. Therefore, five studies falling within the domains of nicotine dependence, sports performance, Autism Spectrum Disorder, and ADHD were considered but, before reviewing them, the next two sections will briefly describe BF and NF techniques in order to provide basics on these two types of training.</p>
</sec>
<sec id="sec2">
<label>2</label>
<title>Biofeedback</title>
<p>Biofeedback is a learning technique that enables an individual to acquire psychophysiological self-regulation skills for the purpose of improving health and/or performance. The main purpose is to achieve voluntary control over involuntary physiological processes within the Central Nervous System (CNS) and Peripheral Nervous System (PNS; <xref ref-type="bibr" rid="ref202">Prinzel et al., 2001</xref>, <xref ref-type="bibr" rid="ref203">2002</xref>; <xref ref-type="bibr" rid="ref58">Demos, 2005</xref>). This control is achieved through an operant conditioning procedure during which the subject receives moment-to-moment, real-time feedback information regarding physiological parameters associated with the cognitive and/or affective states of interest. The feedback is generally provided in the form of visual, auditory or sometimes tactile representations, and through this information, the subject learns to regulate the required levels of physiological activation, gain control over his or her physiological processes and, therefore, optimize his or her psychophysiological functioning (affective, physiological, and cognitive; <xref ref-type="bibr" rid="ref66">Egner and Gruzelier, 2004</xref>; <xref ref-type="bibr" rid="ref239">Sutarto et al., 2010</xref>, <xref ref-type="bibr" rid="ref240">2013</xref>). Common biofeedback techniques include (<xref ref-type="bibr" rid="ref129">Khazan, 2013</xref>):</p>
<list list-type="bullet">
<list-item>
<p>Respiratory biofeedback: measures respiratory rate and pattern, as well as blood carbon dioxide levels, and is used in the treatment of asthma, chronic obstructive pulmonary disease (COPD), anxiety, and hypertension (<xref ref-type="bibr" rid="ref143">Landman et al., 2013</xref>; <xref ref-type="bibr" rid="ref6">Aritzeta et al., 2017</xref>; <xref ref-type="bibr" rid="ref85">Georga et al., 2019</xref>; <xref ref-type="bibr" rid="ref117">Kaja et al., 2020</xref>).</p>
</list-item>
<list-item>
<p>Cardiovascular biofeedback: detects heart rate (HR) and its variability (HRV), respiratory sinus arrhythmia (RSA), and blood flow volume (blood volume pulse, BVP) and is used in the treatment of asthma, chronic obstructive pulmonary disease (COPD) coronary artery disease, depression, fibromyalgia/chronic fatigue syndrome, post-traumatic stress disorder (PTSD), anxiety, chronic pain, and hypertension (<xref ref-type="bibr" rid="ref210">Rosaura Polak et al., 2015</xref>; <xref ref-type="bibr" rid="ref249">Thabrew et al., 2018</xref>; <xref ref-type="bibr" rid="ref73">Fahrenkamp and Benore, 2019</xref>; <xref ref-type="bibr" rid="ref246">Taghizadeh et al., 2019</xref>; <xref ref-type="bibr" rid="ref206">Reneau, 2020</xref>; <xref ref-type="bibr" rid="ref52">da Costa Maynart et al., 2021</xref>; <xref ref-type="bibr" rid="ref261">Vital et al., 2021</xref>).</p>
</list-item>
<list-item>
<p>Neuromuscular biofeedback: provides a measure of muscle tension with surface electromyography (sEMG) and is used to treat fibromyalgia/chronic fatigue syndrome, repetitive strain injury, tinnitus, arthritis, diabetes, pediatric migraine, anxiety, chronic pain, temporomandibular junction disorders, and adult tension headache (<xref ref-type="bibr" rid="ref22">Blume et al., 2012</xref>; <xref ref-type="bibr" rid="ref220">&#x0160;e&#x010D;i&#x0107; et al., 2016</xref>; <xref ref-type="bibr" rid="ref14">Baumueller et al., 2017</xref>; <xref ref-type="bibr" rid="ref145">Lazaridou et al., 2023</xref>).</p>
</list-item>
<list-item>
<p>Skin conductance biofeedback: evaluates the activity of eccrine sweat glands and is used in the treatment of anxiety, hypertension, and car/seasickness (<xref ref-type="bibr" rid="ref67">Elavally et al., 2020</xref>).</p>
</list-item>
<list-item>
<p>Peripheral skin temperature biofeedback: measures the temperature of the fingers and/or toes and is used to treat repetitive strain injury, arthritis, diabetes, migraines, anxiety, chronic pain, hypertension, and Raynaud&#x2019;s disease (<xref ref-type="bibr" rid="ref76">Fiero et al., 2003</xref>; <xref ref-type="bibr" rid="ref123">Karavidas et al., 2006</xref>; <xref ref-type="bibr" rid="ref81">Fritsche et al., 2013</xref>).</p>
</list-item>
<list-item>
<p>Biofeedback of the Central Nervous System (or neurofeedback) which will be described in the next paragraph.</p>
</list-item>
</list>
<p>Biofeedback can include implicit or explicit information (<xref ref-type="bibr" rid="ref138">Kuikkaniemi et al., 2010</xref>; <xref ref-type="bibr" rid="ref177">Nacke et al., 2011</xref>). In the explicit mode, the feedback (visual, auditory or in some cases tactile) is provided directly to the subject so that he himself acts on the biosignal to be regulated; feedback then acts as a direct correlate of this biosignal. Instead, in the implicit mode, the feedback is not explicitly presented to the subject, but generates changes in one or more details of the experimental condition. Therefore, the subject is not directly aware of his biosignal, but obtains implicit access to a correlate of this biosignal as the latter changes the behavior of the system that the subject is observing (e.g., a video game whose content is changes based on the subject&#x2019;s heart rate). Since the studies considered in this review used heart rate variability (HRV) and peripheral skin temperature biofeedback, we will briefly describe only these two modalities.</p>
<sec id="sec3">
<label>2.1</label>
<title>Peripheral skin temperature</title>
<p>Peripheral skin temperature biofeedback measures changes in skin temperature, particularly in the extremities, such as the hands and feet. This form of biofeedback is based on the principle that changes in skin temperature are linked to changes in the autonomic nervous system (ANS), which controls many of the body&#x2019;s involuntary processes. The peripheral temperature depends on the diameter of the arterioles, the small blood vessels that transport blood to the periphery of the body and whose walls contain smooth muscle tissue innervated by the nerves of the sympathetic nervous system. When the sympathetic system is activated (e.g., due to a stress response), a release of norepinephrine occurs, which stimulates the alpha-adrenergic receptors of the smooth muscle tissue of the blood vessels with consequent narrowing of the latter. When blood vessels narrow, blood flow decreases and, consequently, so does skin temperature. Since there is no parasympathetic innervation (e.g., a relaxation response) of the blood vessels (i.e., the parasympathetic nervous system cannot act directly on the blood vessels to cause vasodilation), in order to allow their dilation and, therefore, increase in peripheral temperature, it is necessary to decrease the activity of the sympathetic nervous system, consequently decreasing the amount of norepinephrine that binds to alpha-adrenergic receptors. The subject must then learn to &#x201C;turn off&#x201D; the sympathetic response in order to increase the temperature of the fingers (<xref ref-type="bibr" rid="ref78">Freedman et al., 1983</xref>; <xref ref-type="bibr" rid="ref190">Peper et al., 2009</xref>). During skin temperature biofeedback, sensors are placed on the fingers or toes to measure skin temperature. A computer program then provides visual, auditory or sometimes tactile feedback on temperature changes, with the aim of teaching the subject to increase or decrease the skin temperature at will, voluntarily fibromyalgia.</p>
</sec>
<sec id="sec4">
<label>2.2</label>
<title>Heart rate variability</title>
<p>Heart rate variability (HRV) refers to changes in the time interval between two consecutive heartbeats (<xref ref-type="bibr" rid="ref221">Shaffer and Ginsberg, 2017</xref>). HRV reflects the balance of the ANS (<xref ref-type="bibr" rid="ref222">Shaffer et al., 2014</xref>) and corresponds to the rhythmic accelerations and decelerations of the heartbeat. The heart rate accelerates (i.e., increases) when R-R intervals (i.e., the intervals between beats) shorten and decelerates (i.e., decreases) when R-R intervals lengthen (<xref ref-type="bibr" rid="ref20">Berntson et al., 1997</xref>). These accelerations and decelerations are also referred to as heartbeat oscillations. The amplitude and complexity of these oscillations are an indicator of the body&#x2019;s ability to self-regulate and, according to <xref ref-type="bibr" rid="ref148">Lehrer (2007)</xref>. HRV constitutes a necessary component of the negative feedback mechanism that regulates heart rate and blood pressure. When blood pressure increases, baroreceptors (receptors specialized in sensing pressure within blood vessels) detect this increase and send a signal for the heart rate to slow down, leading to a decrease in blood pressure. However, when blood pressure decreases, the baroreceptors send a signal to increase the heart rate and therefore raise blood pressure. Both heart rate and blood pressure fluctuate continuously to maintain homeostasis, the physiological balance of the body. The baroreceptor reflex therefore constitutes a fundamental component of HRV. The second component is represented by respiratory sinus arrhythmia. HRV oscillations reflect the interaction between the sympathetic and parasympathetic branches of the ANS (<xref ref-type="bibr" rid="ref2">Acharya et al., 2006</xref>). The sympathetic branch increases heart rate, while the parasympathetic branch decreases it. This phenomenon constitutes respiratory sinus arrhythmia, which refers to the fluctuation in heart rate that accompanies breathing: the heart rate increases with inhalation (which activates the sympathetic portion of the ANS) and decreases with exhalation (which activates the parasympathetic portion of the ANS). HRV biofeedback works in a similar way to skin temperature biofeedback but, unlike the latter, provides real-time feedback (visual, auditory, or tactile) of the subject&#x2019;s heart rate variability which, in this way, can learn to achieve control of specific cardiorespiratory processes.</p>
</sec>
<sec id="sec5">
<label>2.3</label>
<title>Electromyography</title>
<p>Surface electromyography (sEMG) consists of measuring the electrical signal produced by muscles during contraction. The source of the electrical signal is the muscle action potential (MAP). MAPs are produced by motor units, i.e., the &#x201C;building blocks&#x201D; of skeletal muscle fibers. Each motor unit consists of a motor neuron in the spinal cord, the muscle fibers it innervates, and an axon that transmits electrical signals from the neuron to the muscle fibers. Once the neuron sends the electrical signal to the axon, it releases the neurotransmitter acetylcholine, which stimulates the muscle to contract. This communication process between the spinal cord and the muscle is achieved through the MAP, i.e., a change in the electrical charge of the muscle cell membrane from a resting value of approximately &#x2212;70&#x2009;mV to a peak of approximately +30&#x2009;mV, the potential d&#x2018;action. The amplitude of the signal that the biofeedback equipment collects from the muscles depends on the number of action potentials generated, the firing rate of each active neuron and the amount of fatty tissue between the electrode and the muscle. The more adipose tissue between the muscle and the electrode, the smaller the recorded signal will be. Since the amplitude of the recorded sEMG signal depends on the number of active neurons, the innervation rate (i.e., the number of muscle fibers controlled by a single motor neuron) plays an important role in determining how large the amplitude of the sEMG signal will be. Motor units responsible for large, powerful movements innervate a greater number of muscle fibers, while those responsible for fine movements innervate fewer muscle fibers. The greater the number of muscle fibers that the neuron controls, the greater the innervation rate, the more powerful the movement produced by that muscle and the greater the amplitude of the sEMG signal. As regard the placement of the electrodes during sEMG biofeedback, once the muscles being trained have been identified, it is necessary to decide whether to use a narrow or wide electrode placement. sEMG records electrical activity from muscles between two active electrodes and, as highlighted by <xref ref-type="bibr" rid="ref225">Sherman (2003)</xref>, the electrical signal that triggers muscle contraction in one area also influences electrical activity in adjacent areas. Therefore, the electrical activity generated by muscles underlying and adjacent to the target muscle could also be recorded. Therefore, the wider the positioning of the active electrodes, the greater the number of muscles whose signal will be acquired and the greater the amplitude of the sEMG signal recorded and shown. Narrow placement (approximately 2&#x2009;cm or less between active electrodes) is appropriate when you want to work with a specific muscle, minimizing cross talk between muscles, i.e., signals from adjacent or underlying muscles. A wider positioning, however, is appropriate for the relaxation of large groups of muscles, as you want to obtain as much information as possible regarding the muscular activity in the area of interest. Finally, in relation to the steps to follow for sEMG biofeedback training, after having identified the target muscle or muscles, we move on to positioning the electrodes based on the type of training you want to carry out. For example, if you want to isolate the activity of a target muscle, you place one set of electrodes on the muscle of interest and the other set on the muscle that co-contracts unnecessarily together with the muscle of interest. At this point the subject is asked to increase the tension in the muscle of interest and to observe what happens to the muscle that co-contracts. The purpose of this training is to teach the subject to activate the target muscle and to reduce the activation of the co-contracting muscle, through the use of real-time auditory or visual feedback (for example, the sEMG signal shown on the monitor screen computer) through which the subject, over the course of several sessions, learns to control his own muscle activation.</p>
</sec>
</sec>
<sec id="sec6">
<label>3</label>
<title>Neurofeedback</title>
<p>Neurofeedback (NF) is a form of biofeedback based on characteristics of brain activity. This is a technique that has been extensively studied over the last few decades and whose foundations have been laid since the 1930s. In fact, in the middle of these years, some groups of researchers trained subjects to block alpha waves through a classical conditioning mechanism (<xref ref-type="bibr" rid="ref65">Durup and Fessard, 1935</xref>; <xref ref-type="bibr" rid="ref157">Loomis et al., 1936</xref>). Subsequently, in a 1941 study, <xref ref-type="bibr" rid="ref115">Jasper and Shagass (1941)</xref> demonstrated, for the first time, that the alpha rhythm could be suppressed voluntarily, thus bringing to light the concept of &#x201C;voluntary control&#x201D; of electroencephalographic activity. For the use of operant conditioning to modulate EEG activity (i.e., using the information derived from the EEG as a reward to be provided to the subject in real time) we had to wait until the 1960s (<xref ref-type="bibr" rid="ref7">Arns, 2010</xref>; <xref ref-type="bibr" rid="ref237">Sterman et al., 2010</xref>; <xref ref-type="bibr" rid="ref120">Kamiya, 2011</xref>). Since that time this technique has been increasingly used for the treatment of various neuropsychiatric conditions (ADHD, epilepsy, stroke, developmental disabilities, migraines, insomnia, etc.), definitively establishing the birth of what we know today as Neurofeedback. In 2011, Hammond describes seven types of neurofeedback, which can be used to treat different conditions:</p>
<list list-type="order">
<list-item>
<p>The frequency/power NF (or EEG-NF): modifies the amplitude or speed of specific frequency bands within specific brain regions. For this purpose, electrodes placed on the surface of the subject&#x2019;s scalp are typically used and it is a technique classically used in the treatment of ADHD, learning disorders, anxiety, insomnia and other pathological and non-pathological conditions (for example, in improving sports performance; <xref ref-type="bibr" rid="ref215">Salimnejad et al., 2019</xref>; <xref ref-type="bibr" rid="ref89">Gong et al., 2021</xref>).</p>
</list-item>
<list-item>
<p>The Slow Cortical Potential NF (SCP-NF): modifies the direction (positive or negative) of slow cortical potentials and is used to treat ADHD, migraines, and epilepsy (<xref ref-type="bibr" rid="ref35">Christiansen et al., 2014</xref>).</p>
</list-item>
<list-item>
<p>The Low-Energy Neurofeedback System (LENS): uses a very weak electromagnetic signal to modify the subject&#x2019;s brain waves while the latter is in a condition of immobility and with his eyes closed (<xref ref-type="bibr" rid="ref269">Zandi-Mehran et al., 2014</xref>). This technique is considered a passive form of NF and has been used to treat conditions as diverse as head trauma, ADHD, insomnia, fibromyalgia, restless legs syndrome, anxiety, depression, and anger.</p>
</list-item>
<list-item>
<p>NF with Hemoencephalography (HEG): provides feedback regarding cerebral blood flow and is used to treat migraine (<xref ref-type="bibr" rid="ref60">Dias et al., 2012</xref>).</p>
</list-item>
<list-item>
<p>The Live Z-Score NF: involves the continuous comparison of several variables related to brain electrical activity (e.g., power, coherence, and asymmetry) with a normative database to provide moment-to-moment feedback and is used to treat insomnia (<xref ref-type="bibr" rid="ref44">Collura et al., 2010</xref>).</p>
</list-item>
<list-item>
<p>Low Resolution Electromagnetic Tomography (LORETA): uses 19 electrodes to monitor phase, power and coherence (<xref ref-type="bibr" rid="ref187">Pascual-Marqui et al., 1994</xref>) and is used for addictions, depression and obsessive-compulsive disorder.</p>
</list-item>
<list-item>
<p>Functional Magnetic Resonance Imaging NF (fMRI-NF): uses the activity of the subcortical areas of the brain as feedback (<xref ref-type="bibr" rid="ref150">L&#x00E9;vesque et al., 2006</xref>; <xref ref-type="bibr" rid="ref112">Hurt et al., 2014</xref>).</p>
</list-item>
</list>
<p>To understand the functioning of the NF, reference must be made to learning processes, which occur thanks to a brain capacity known as neuronal plasticity (<xref ref-type="bibr" rid="ref133">Kolb, 1995</xref>; <xref ref-type="bibr" rid="ref161">Maren and Baudry, 1995</xref>; <xref ref-type="bibr" rid="ref211">Rosenzweig and Bennett, 1996</xref>), based on neuromodulation and on long-term potentiation (LTP; <xref ref-type="bibr" rid="ref1">Abarbanel, 1995</xref>). It has been proposed that during NF training, the relevant neural networks are modified through the process of neuromodulation (<xref ref-type="bibr" rid="ref70">Evans and Abarbanel, 1999</xref>) and that these changes are consolidated through LTP triggered by continuous feedback activity during this training (<xref ref-type="bibr" rid="ref70">Evans and Abarbanel, 1999</xref>; <xref ref-type="bibr" rid="ref236">Sterman and Egner, 2006</xref>).</p>
<p>Recent discussions &#x0456;n the field &#x043E;f neurofeedback have often centered &#x043E;n the role &#x043E;f long-term potentiation (LTP) as a foundational mechanism underlying the efficacy &#x043E;f NF training protocols (<xref ref-type="bibr" rid="ref83">Gabrielsen et al., 2022</xref>; <xref ref-type="bibr" rid="ref235">Spreyermann, 2022</xref>). LTP, characterized by the long-lasting strengthening &#x043E;f synapses based &#x043E;n recent patterns &#x043E;f activity, has been widely recognized for its role &#x0456;n learning and memory within the neuroscience community. However, the complexity &#x043E;f neural responses elicited by NF protocols such as Alpha/Theta (A/T) and Infra-Low Frequency (ILF) NF suggests that a broader spectrum &#x043E;f neuroplastic mechanisms may be at play. Unlike traditional models that primarily focus &#x043E;n LTP&#x2019;s role &#x0456;n synaptic efficacy, A/T and ILF NF protocols exemplify how NF can modulate broader neural networks and states. This modulation does not solely rely &#x043E;n the strengthening &#x043E;f synaptic connections but also involves the induction &#x043E;f desirable brain states and the balance &#x043E;f neural oscillations across various frequency bands (<xref ref-type="bibr" rid="ref175">Mu&#x00F1;oz-Moldes and Cleeremans, 2020</xref>).</p>
<p>In this review, we will only consider EEG-NFB, as the included articles exclusively used this technique. During NF training, electrophysiological processes provide the basis for information transmission, whereby brain oscillations present in specific cortical areas reflect cognitive processes. These brain oscillations are divided into different frequency bands: delta (0.5&#x2013;4&#x2009;Hz), theta (4&#x2013;8&#x2009;Hz), alpha (8&#x2013;13&#x2009;Hz), beta (15&#x2013;30&#x2009;Hz), and gamma (&#x003E; 30&#x2009;Hz). In a classic NF set-up, EEG activity is recorded using a referential (or monopolar) montage. During an NF session, a real-time analysis of EEG frequencies is shown to provide information regarding the amplitude of activity within each of the different frequency bands. Once the desired changes in the electrophysiological patterns of interest have been produced, the subject will receive a reward in the form of an auditory, visual or even tactile signal. During numerous training sessions, the participant will learn to develop strategies to consciously and voluntarily modify and self-regulate their brain electrical activity. Neurofeedback therefore constitutes neurocognitive training based on the principles of operant conditioning and over the years has found application in the treatment of various psychopathological conditions and in the improvement of cognitive and motor performance.</p>
<p>There are several protocols that can be used for NF training:</p>
<list list-type="bullet">
<list-item>
<p>The alpha protocol consists of the enhancement or inhibition of this frequency band and is used in the treatment of pain and brain trauma, to reduce anxiety and stress and to improve cognitive performance (e.g., memory and functions executive).</p>
</list-item>
<list-item>
<p>The beta protocol is based on the enhancement of this frequency band, usually in association with the simultaneous inhibition of the theta frequency band, and is used in the treatment of ADHD, epilepsy and autism spectrum disorders and in the improvement of attention and concentration.</p>
</list-item>
<list-item>
<p>The alpha/theta protocol has the function of enhancing the theta frequency band compared to the alpha band and is used to reduce stress and for the treatment of anxiety and addictions.</p>
</list-item>
<list-item>
<p>The delta protocol consists of the enhancement or inhibition of this frequency band and is used in the treatment of ADHD and learning disabilities and to reduce depressive and anxious states and pain (e.g., headaches and migraines) and improve the quality of sleep.</p>
</list-item>
<list-item>
<p>The theta protocol focuses on the enhancement of this frequency band, in particular in the frontal-medial region (frontal-midline theta, FMT) and is used to improve motor performance (e.g., the flow experience) and cognitive performance (e.g., e.g., executive functions).</p>
</list-item>
<list-item>
<p>The Infra-Low Frequency (ILF) protocol targets the very low-frequency brain waves, often below 0.1&#x2009;Hz, engaging with the foundational aspects &#x043E;f brain function. ILF Neurofeedback &#x0456;s particularly noted for its potential &#x0456;n stabilizing the nervous system, thereby contributing t&#x043E; improvements &#x0456;n emotional regulation, stress reduction, and overall cognitive function. Its application spans a wide range &#x043E;f conditions, leveraging the deep and often subconscious levels &#x043E;f neural activity t&#x043E; facilitate therapeutic change. This protocol exemplifies the advanced frontier &#x043E;f neurofeedback research, exploring how subtle modulations &#x0456;n brain activity can yield significant health benefits (<xref ref-type="bibr" rid="ref62">Doren et al., 2018</xref>).</p>
</list-item>
</list>
<p>After discussing the various NF training protocols, such as alpha, beta, delta, and theta protocols, it is pertinent t&#x043E; delve deeper into the nuanced mechanisms &#x043E;f action behind these methods. Specifically, Alpha/Theta Neurofeedback and Infra-Low Frequency (ILF) Neurofeedback diverge from these protocols by focusing &#x043E;n state feedback rather than learning reinforcement. Alpha/Theta Neurofeedback &#x0456;s designed t&#x043E; induce a relaxed &#x043E;r meditative state, enhancing therapeutic outcomes through the modulation &#x043E;f brain states. Similarly, ILF Neurofeedback targets the autonomic nervous system, aiming t&#x043E; achieve a balanced physiological state. This delineation underscores the unique therapeutic potential &#x043E;f these modalities beyond the classical operant conditioning frameworks, highlighting their distinct approach t&#x043E; facilitating therapeutic change. Alpha/Theta Neurofeedback aims t&#x043E; induce a relaxed &#x043E;r meditative state, enhancing therapeutic outcomes through state feedback rather than learning reinforcement traditionally associated with neurofeedback. Similarly, ILF Neurofeedback focuses &#x043E;n modulating the autonomic nervous system t&#x043E; promote a balanced physiological state. This distinction highlights the unique mechanisms &#x043E;f action for these neurofeedback modalities, underscoring their therapeutic potential beyond classical operant conditioning frameworks.</p>
<p>Building &#x043E;n the discussion &#x043E;f various neurofeedback (NF) training protocols, &#x0456;t &#x0456;s crucial t&#x043E; address the potential for personalization within these therapeutic modalities. The concept &#x043E;f tailoring NF procedures t&#x043E; individual characteristics, as exemplified by M. Arns with Q-based NF and the symptom and state change-based individualization pioneered by the Othmer group, represents a significant advancement &#x0456;n the field. This approach underscores the importance &#x043E;f adapting NF protocols t&#x043E; meet the unique neurophysiological and psychological profiles &#x043E;f each individual, potentially transforming non-responders into responders.</p>
<p>The variability &#x0456;n response t&#x043E; standard NF protocols highlights the necessity for a more nuanced approach. Personalization can involve adjusting the training parameters based &#x043E;n quantitative EEG (qEEG) analyses, as done &#x0456;n Q-based NF, &#x043E;r modifying protocols based &#x043E;n symptomatic and state changes observed during the training process. Such individualized strategies not only cater t&#x043E; the specific needs &#x043E;f the participants but also optimize the chances &#x043E;f therapeutic success.</p>
<p>The results of NF training, however, are not always consistent. There is, in fact, a significant part of the population subjected to this treatment who does not seem to benefit from its effects and who does not achieve the required voluntary control of the frequency bands covered by the training, the so-called non-responders (or non-performers or non -regulators; <xref ref-type="bibr" rid="ref264">Weber et al., 2010</xref>; <xref ref-type="bibr" rid="ref4">Alkoby et al., 2018</xref>). In this regard, two categories of predictive factors of the ineffectiveness of NF training have been identified: psychological predictors and neurophysiological predictors. Regarding the former, <xref ref-type="bibr" rid="ref267">Witte et al. (2013)</xref> showed that subjects&#x2019; beliefs regarding their ability to control technological devices can predict performance in NF training, while <xref ref-type="bibr" rid="ref132">Kober et al. (2013)</xref> found an influence of the mental strategies used by subjects to control the bars that reflect their brain activity in real time. The authors found that the mental strategy used in NF sessions depended on the brain parameter chosen for training. For example, for the SMR protocol the participants who had not used mental strategies showed a better performance, while for the gamma protocol the mental strategy adopted showed no influence on performance. As regard neurophysiological predictors, <xref ref-type="bibr" rid="ref263">Wan et al. (2014)</xref> showed that alpha wave amplitude in resting condition before NF training significantly correlated with success in EEG learning. Also confirmed by other studies (e.g., <xref ref-type="bibr" rid="ref135">Kotchoubey et al., 1999</xref>; <xref ref-type="bibr" rid="ref181">Neumann and Birbaumer, 2003</xref>; <xref ref-type="bibr" rid="ref264">Weber et al., 2010</xref>), this observation has led to considering individual differences in the amplitude of the different frequency bands as a factor not to be underestimated within NF training. What we therefore asked ourselves is whether a personalization of NF procedures, in which the characteristics of the training are adapted to the individual, can transform non-responders into responders. For example, two different studies (<xref ref-type="bibr" rid="ref13">Bauer, 1976</xref>; <xref ref-type="bibr" rid="ref178">Nan et al., 2012</xref>), both aimed at improving performance in the digit span task following NF training aimed at the alpha frequency band, obtained opposite results: <xref ref-type="bibr" rid="ref13">Bauer (1976)</xref>, who used a fixed alpha band width, did not obtain improvements in subjects&#x2019; performance; while <xref ref-type="bibr" rid="ref178">Nan et al. (2012)</xref>, who used the individual alpha frequency (IAF; that is, they calculated the alpha band for each participant), observed improvements in the subjects in the same test used by Bauer. This demonstrated the need to adapt NF training to the specific characteristics of each subject&#x2019;s brain electrical activity. A second property to check is the type of feedback to use (visual, auditory, or tactile). For example, <xref ref-type="bibr" rid="ref167">Mathiak et al. (2015)</xref> studied the effect of using &#x201C;social&#x201D; feedback (a smiling avatar) on the ability to control an EEG frequency during NF training. The authors showed that social feedback produced greater activation in the anterior cingulate cortex and reward-related circuits compared to standard feedback (a moving bar). Furthermore, the use of this type of feedback improved the subjects&#x2019; ability to control the frequency bands trained during the NF procedure. Therefore, using a type of personalized feedback, based on the subject&#x2019;s characteristics, could lead to a better performance in the training. Finally, the last characteristic that must be taken into consideration is the type of mental strategy to employ. For example, <xref ref-type="bibr" rid="ref178">Nan et al. (2012)</xref> showed that thinking about pleasant situations or people (e.g., thinking about family and friends) represents an efficient mental strategy to enhance the alpha frequency band, while <xref ref-type="bibr" rid="ref105">Hardman et al. (1997)</xref> and <xref ref-type="bibr" rid="ref132">Kober et al. (2013)</xref> showed that the best way to make NF training effective, respectively, at slow cortical potential (SCP) and sensorimotor rhythm (SMR), is to not use any mental strategy. Therefore, customizing the type of mental strategy based on both the type of NF protocol and the individual&#x2019;s characteristics could lead to better performance in NF training.</p>
</sec>
<sec id="sec7">
<label>4</label>
<title>Clarification &#x043E;n the relationship and integration &#x043E;f BF and NF techniques</title>
<p>In the context &#x043E;f our review, &#x0456;t &#x0456;s essential t&#x043E; delineate the interrelation between BF and NF. While both modalities leverage the principle &#x043E;f feedback for self-regulation, their application domains and mechanisms &#x043E;f action differ. BF techniques facilitate control over various physiological processes, potentially including but not limited t&#x043E; cardiovascular, respiratory, and musculoskeletal systems. In contrast, NF exclusively focuses &#x043E;n modulating brain functions, offering a targeted approach t&#x043E; influence cognitive and psychological states.</p>
<p>It &#x0456;s crucial t&#x043E; note that the integration &#x043E;f these techniques can be implemented either &#x0456;n parallel &#x043E;r sequentially. In a parallel approach, BF and NF are applied simultaneously during the same treatment session, allowing the patient t&#x043E; receive feedback &#x043E;n both peripheral physiological parameters (such as heart rate variability &#x043E;r muscle tension &#x0456;n the case &#x043E;f BF) and brain activity (such as brain waves &#x0456;n the case &#x043E;f NF). This approach aims t&#x043E; maximize the treatment&#x2019;s effectiveness by synergizing the effects &#x043E;f both techniques. Alternatively, a sequential approach involves applying NF and BF &#x0456;n separate sessions, with the order &#x043E;f administration varying (first NF then BF, &#x043E;r vice versa). This method can be particularly useful for addressing specific patient needs, allowing for a greater focus &#x043E;n areas &#x043E;f intervention identified at different stages &#x043E;f the treatment. Both approaches have the potential t&#x043E; offer unique benefits, and the choice between parallel &#x043E;r sequential application should be guided by the specific needs &#x043E;f the patient, the conditions being treated, and the therapeutic objectives defined by the practitioner. Future research should further investigate the conditions under which each approach may be more advantageous, thus contributing t&#x043E; greater customization and effectiveness &#x043E;f treatments integrating BF and NF.</p>
<p>Our exploration into the combined use &#x043E;f BF and NF &#x0456;s predicated &#x043E;n the hypothesis that integrating these techniques can harness their respective strengths, potentially amplifying therapeutic and performance outcomes. By concurrently addressing the CNS and PNS, the integrated approach aims t&#x043E; promote a more comprehensive state &#x043E;f self-regulation, enhancing both mental and physical well-being. Our review seeks t&#x043E; contribute new insights into how this synergistic application &#x043E;f BF and NF might differ &#x0456;n effectiveness from using multiple BF techniques &#x0456;n isolation. By examining studies that implement this integrated methodology, we aspire t&#x043E; uncover distinct benefits that could redefine best practices &#x0456;n biofeedback applications for therapeutic and performance enhancement purposes.</p>
</sec>
<sec id="sec8">
<label>5</label>
<title>The integrated BF&#x2009;+&#x2009;NF approach</title>
<p>In the following paragraphs, we will examine the effectiveness of an integrated BF&#x2009;+&#x2009;NF training based on the results present in the literature.</p>
<sec id="sec9">
<label>5.1</label>
<title>Nicotine addiction</title>
<p>According to a study published in 2021 in The Lancet, there were an estimated 1.4 billion smokers worldwide in 2019 (<xref ref-type="bibr" rid="ref205">Reitsma et al., 2021</xref>). Smoking impacts all organs of the body and is the cause of numerous premature deaths and diseases (especially oncological and cardiovascular diseases; US Preventive Services Task Force, <xref ref-type="bibr" rid="ref182">Owens et al., 2020</xref>). Chronic nicotine use has been associated with both functional and structural impairments of the Central Nervous System (<xref ref-type="bibr" rid="ref197">Pomerleau, 1992</xref>; <xref ref-type="bibr" rid="ref176">Musso et al., 2007</xref>; <xref ref-type="bibr" rid="ref91">Goriounova and Mansvelder, 2012</xref>; <xref ref-type="bibr" rid="ref75">Fedota and Stein, 2015</xref>; <xref ref-type="bibr" rid="ref241">Sutherland et al., 2016</xref>) and several studies have reported atrophy of white and gray matter especially in the frontal, prefrontal, temporal, fronto-parietal areas and in the cingulate and cerebellar cortices (<xref ref-type="bibr" rid="ref28">Brody et al., 2004</xref>; <xref ref-type="bibr" rid="ref84">Gallinat et al., 2006</xref>; <xref ref-type="bibr" rid="ref242">Swan and Lessov-Schlaggar, 2007</xref>; <xref ref-type="bibr" rid="ref137">K&#x00FC;hn et al., 2012</xref>). Networks involved in cognition and executive functions, such as the Default Mode Network (DMN), have been shown to be affected by addiction (<xref ref-type="bibr" rid="ref110">Hong et al., 2009</xref>; <xref ref-type="bibr" rid="ref265">Weiland et al., 2015</xref>). The prefrontal networks involved in attention show a decrease in activity at least partly related to the duration of nicotine addiction (<xref ref-type="bibr" rid="ref176">Musso et al., 2007</xref>) and a disorganization of the network topology characterized by a decrease in the efficiency of the DMN has been shown and other brain networks (<xref ref-type="bibr" rid="ref152">Lin et al., 2015</xref>). These CNS alterations, which also include increased resting connectivity in prefrontal areas involved in reward circuits (<xref ref-type="bibr" rid="ref113">Janes et al., 2012</xref>), may help explain, at least in part, why interventions aimed at extinguishing reward addiction nicotine continue to be difficult or even ineffective (<xref ref-type="bibr" rid="ref9">Ashare et al., 2014</xref>). Furthermore, the greatest challenge in nicotine addiction cessation programs consists in the prevention of relapses, which are triggered, among other things, by negative affective states and conditions related to anxiety and stress, smoking being often used as a means to deal with these situations (<xref ref-type="bibr" rid="ref185">Pandria et al., 2018</xref>). Therefore, ex-smokers need alternative coping strategies (<xref ref-type="bibr" rid="ref25">Brandon et al., 1990</xref>; <xref ref-type="bibr" rid="ref49">Crevenna, 2010</xref>; <xref ref-type="bibr" rid="ref183">Pandria et al., 2020</xref>).</p>
<p>In addition to pharmacological interventions, whose side effects however constitute the main reason for their discontinuation (<xref ref-type="bibr" rid="ref266">Williams et al., 2007</xref>; <xref ref-type="bibr" rid="ref101">Halperin et al., 2009</xref>), alternative approaches have also been used to address substance addiction (nicotine included), such as behavioral therapies and biofeedback and neurofeedback programs. BF and NF training have been shown to be effective in the management of anxiety disorders, depression and stress-related conditions (<xref ref-type="bibr" rid="ref102">Hammond, 2005</xref>; <xref ref-type="bibr" rid="ref99">Gruzelier et al., 2014</xref>; <xref ref-type="bibr" rid="ref245">Tabachnick, 2015</xref>) and have been used since the 1970s, in the treatment of addictions (<xref ref-type="bibr" rid="ref142">Lamontagne et al., 1977</xref>; <xref ref-type="bibr" rid="ref57">DeGood and Valle, 1978</xref>).</p>
<p>For instance, given the significant challenge posed by alcohol dependence, particularly with relapse rates reaching up t&#x043E; 80%, the integration &#x043E;f neurofeedback (NF) and biofeedback (BF) &#x0456;n treatment protocols offers a promising avenue for intervention. Although some addiction facilities have begun t&#x043E; implement NF/BF approaches, the current deployment &#x0456;s not commensurate with the high prevalence and relapse rates associated with alcohol dependence. This disparity underscores a critical need for expanding and intensifying the use &#x043E;f NF/BF &#x0456;n addiction treatment programs.</p>
<p>The early work &#x043E;f Penniston &#x0456;n the realm &#x043E;f Alpha/Theta (A/T) neurofeedback for alcohol dependence highlights the potential &#x043E;f such personalized interventions. Initially utilizing thermal and Skin Conductance Level (SCL) feedback, Penniston&#x2019;s approach evolved t&#x043E; incorporate NF techniques, setting a foundational precedent for integrating various biofeedback modalities &#x0456;n treating addiction (<xref ref-type="bibr" rid="ref188">Peniston and Kulkosky, 1989</xref>). This multidimensional feedback strategy not only addresses the physiological aspects &#x043E;f addiction but also engages deeper psychological patterns associated with relapse.</p>
<p>These approaches have been shown to be encouraging in facilitating the self-regulation of relapse-related factors, such as craving and stress (<xref ref-type="bibr" rid="ref31">Canterberry et al., 2013</xref>; <xref ref-type="bibr" rid="ref104">Hanlon et al., 2013</xref>; <xref ref-type="bibr" rid="ref151">Li et al., 2013</xref>; <xref ref-type="bibr" rid="ref130">Kim et al., 2015</xref>; <xref ref-type="bibr" rid="ref107">Hartwell et al., 2016</xref>; <xref ref-type="bibr" rid="ref29">Bu et al., 2019</xref>) and can positively influence the degree of nicotine dependence and the presence of psychiatric symptoms (<xref ref-type="bibr" rid="ref185">Pandria et al., 2018</xref>).</p>
<p>In a recent 2023 study, Pandria and colleagues used an integrated BF&#x2009;+&#x2009;NF approach to evaluate its effects on extinguishing nicotine addiction. The intervention aimed to combine an increase in vasodilation through a BF training of peripheral skin temperature (<xref ref-type="bibr" rid="ref255">Tolin et al., 2020</xref>) and a facilitation of a state of deep relaxation through a NF training targeted at the alpha and theta (<xref ref-type="bibr" rid="ref95">Gruzelier, 2009</xref>, <xref ref-type="bibr" rid="ref96">2014a</xref>,<xref ref-type="bibr" rid="ref97">b</xref>,<xref ref-type="bibr" rid="ref98">c</xref>). The BF training of skin temperature was chosen as this constitutes a reliable marker of stress which, as previously mentioned, plays a primary role in nicotine addiction (<xref ref-type="bibr" rid="ref125">Kassel et al., 2003</xref>; <xref ref-type="bibr" rid="ref256">Tsourtos et al., 2008</xref>) and it is also influenced by nicotine itself through its stimulatory action on the sympathetic system, causing peripheral vasoconstriction (<xref ref-type="bibr" rid="ref18">Benowitz and Burbank, 2016</xref>). The alpha-theta NF protocol was instead chosen as it has been successfully applied in other forms of addiction (<xref ref-type="bibr" rid="ref188">Peniston and Kulkosky, 1989</xref>; <xref ref-type="bibr" rid="ref166">Masterpasqua and Healey, 2003</xref>; <xref ref-type="bibr" rid="ref219">Scott et al., 2005</xref>; <xref ref-type="bibr" rid="ref233">Sokhadze et al., 2008</xref>), in PTSD (<xref ref-type="bibr" rid="ref189">Peniston and Kulkosky, 1991</xref>) and in improving mood (<xref ref-type="bibr" rid="ref204">Raymond et al., 2005</xref>).</p>
<p>The study participants (17 smokers) underwent a multi-phase intervention. The baseline evaluation (baseline, T0) consisted of a first clinical and behavioral examination and a second electrophysiological and neuropsychological investigation. Subsequently, five BF training sessions were administered and, immediately afterwards, the participants underwent an intermediate evaluation (T1), at the end of which the alpha-theta NF protocol was administered, divided into 20 sessions. Finally, participants underwent the last survey (T2). The results of this integrated study showed a reduction in participants&#x2019; exhaled carbon monoxide (CO) levels and a decrease in total oxidative stress (TOS) levels. Smoking in fact leads to an increase in oxidative damage (<xref ref-type="bibr" rid="ref119">Kamceva et al., 2016</xref>; <xref ref-type="bibr" rid="ref122">Karademirci et al., 2018</xref>) which leads to the generation of free radicals and inflammatory responses (<xref ref-type="bibr" rid="ref51">Csordas and Bernhard, 2013</xref>; <xref ref-type="bibr" rid="ref170">Messner and Bernhard, 2014</xref>) and has been shown that there is a correlation between oxidative stress and the number of cigarettes smoked (<xref ref-type="bibr" rid="ref119">Kamceva et al., 2016</xref>). From these results we could suggest a protective role of BF&#x2009;+&#x2009;NF training against the oxidative load induced by smoking, as the participants in the study by <xref ref-type="bibr" rid="ref184">Pandria et al. (2023)</xref> who were highly dependent on nicotine still managed to achieve a significant reduction in oxidative stress levels. Smoking also causes dysregulation of hormonal responses to stress (<xref ref-type="bibr" rid="ref34">Childs and de Wit, 2009</xref>), leading to the establishment of abnormal anxiety thresholds. As argued by <xref ref-type="bibr" rid="ref118">Kalantzi-Azizi and Degleris (1992)</xref> and <xref ref-type="bibr" rid="ref186">Parrott (1998)</xref>, the variation in mood during both long and short periods of abstinence leads to conditioned learning, whereby abstinence and other negative affective states can be interpreted as stressors that lead to the act of smoking which, in turn, alleviates withdrawal symptoms and negative affective states, creating a vicious circle. Therefore, as argued by <xref ref-type="bibr" rid="ref185">Pandria et al. (2018)</xref>, stress constitutes a central element in nicotine addiction. In the study examined for this narrative review, positive changes were observed in relation to stress, as a reduction in the scores in the State&#x2013;Trait Anxiety Inventory was noted, in particular in the items relating to trait anxiety, confirming what <xref ref-type="bibr" rid="ref248">Taylor et al. (2014)</xref> claimed namely that quitting smoking reduces anxiety, stress and depressive symptoms, improving mood. BF&#x2009;+&#x2009;NF training has also proven effective in improving self-esteem, particularly in women and in participants with a strong nicotine addiction, subjects who, according to some studies, are characterized by a low level of self-esteem (<xref ref-type="bibr" rid="ref50">Croghan et al., 2006</xref>; <xref ref-type="bibr" rid="ref100">Guillon et al., 2007</xref>). Although a negative correlation between self-esteem and smoking has not yet been demonstrated (<xref ref-type="bibr" rid="ref244">Szinay et al., 2019</xref>), according to <xref ref-type="bibr" rid="ref79">Freijy and Kothe (2013)</xref> high levels of self-esteem lead to a greater likelihood of quitting smoking.</p>
<p>In addition, BF&#x2009;+&#x2009;NF training produced positive results in improving inhibitory control, visual attention, task switching, and working memory, assessed through the Stroop test, Trail A test, and Digit Span, respectively. Although some studies believe that nicotine promotes cognitive improvement through stimulation of brain areas related to cognition (<xref ref-type="bibr" rid="ref48">Couey et al., 2007</xref>; <xref ref-type="bibr" rid="ref128">Kenney and Gould, 2008</xref>; <xref ref-type="bibr" rid="ref262">Wallace and Bertrand, 2013</xref>; <xref ref-type="bibr" rid="ref140">Kutlu and Gould, 2015</xref>), there are no there is still clear evidence to support this thesis, as the cognitive improvement could simply be given by the relief from withdrawal symptoms (<xref ref-type="bibr" rid="ref108">Heishma et al., 1994</xref>; <xref ref-type="bibr" rid="ref109">Heishman, 1998</xref>). Finally, this study showed neuroplasticity capacity in the group of smokers subjected to integrated training, which showed increased synchronization especially between the networks involved in cognitive control (frontoparietal network, FPN), in goal-directed behavior (DMN) and in visual processing (visual network, VIS). The increased synchronization between the visual network and other resting-state networks (RSNs) is considered an indicator of better integration of sensory information (<xref ref-type="bibr" rid="ref61">Dobrushina et al., 2020</xref>). Finally, <xref ref-type="bibr" rid="ref172">Modi et al. (2015)</xref> found that trait anxiety is associated with reduced connectivity between the DMN and the VIS, thus the reduction in STAI trait anxiety scores observed in the study by <xref ref-type="bibr" rid="ref184">Pandria et al. (2023)</xref> it may reflect the increase in connectivity observed in these two networks.</p>
<p>The effectiveness of EEG-NF training in the treatment of nicotine addiction has also been documented by recent reviews (<xref ref-type="bibr" rid="ref183">Pandria et al., 2020</xref>; <xref ref-type="bibr" rid="ref126">Keilani et al., 2022</xref>). <xref ref-type="bibr" rid="ref92">Griffith and Crossman's (1983)</xref> study used an NF intervention targeting the alpha frequency band and showed that, while smoking a cigarette, all smokers had decreased occipital alpha activity, and immediately after smoking, five smokers of six showed a continuous increase in heart rate and four a decrease in skin temperature. Furthermore, during the NF training, four out of six smokers managed to increase their alpha activity, two participants stopped smoking at the end of the 6-month follow-up period and the other four reduced their daily number of cigarettes. The study by <xref ref-type="bibr" rid="ref29">Bu et al. (2019)</xref> also showed a notable decrease in the number of cigarettes smoked per day, as well as a significant improvement in craving scores and a significant reduction in the amplitude of the P300 event-related potential (ERP), related to craving and smoking (<xref ref-type="bibr" rid="ref155">Littel and Franken, 2011</xref>; <xref ref-type="bibr" rid="ref71">Evans et al., 2013</xref>). The review by <xref ref-type="bibr" rid="ref185">Pandria et al. (2018)</xref> also took into consideration the study by <xref ref-type="bibr" rid="ref243">Szalai et al. (1986)</xref>, which used an alpha frequency band modulation protocol and divided the participants into 10 deprived smokers (DS) and in 10 non-deprived smokers (NDS) including, as active controls, ex-smokers (EF), and non-smokers (NS). This study showed that deprived smokers and non-smokers were able to reduce the amplitude of the alpha frequency band during a backward memory task, while deprived smokers were able to reduce the alpha frequency band even during the alpha suppression condition &#x201C;alpha rhythm.&#x201D; Furthermore, only non-smokers were able to increase alpha amplitude during the alpha rhythm-enhanced condition, while non-deprived smokers showed a significant reduction during this task.</p>
<p>However, regarding the effectiveness of peripheral skin temperature BF in the treatment of nicotine addiction, the study by <xref ref-type="bibr" rid="ref185">Pandria et al. (2018)</xref>, reviewed by <xref ref-type="bibr" rid="ref183">Pandria et al. (2020)</xref> and by <xref ref-type="bibr" rid="ref126">Keilani et al. (2022)</xref>, used finger temperature as BF training with the aim of having participants gain control over ANS functions. The results showed positive effects of BF on the ability to control skin temperature and a significant improvement (in males, but not in females) in the degree of nicotine dependence, measured with the Fagerstr&#x00F6;m test, and in the score of the General Health Questionnaire. Furthermore, a reduction in the presence of psychiatric symptoms, anxiety, depression, and withdrawal symptoms was observed, while an increase in self-esteem was observed. Finally, a reduction in the number of participants with moderate and severe addiction was noted. The second study taken into consideration in the review by <xref ref-type="bibr" rid="ref183">Pandria et al. (2020)</xref> is that of <xref ref-type="bibr" rid="ref94">Grimsley (1990)</xref>, which aimed to compare the ability to increase the skin temperature of the hand between smokers and non-smokers and used three groups of subjects: smokers who smoked before the BF session (SS), smokers who did not smoke before the session (SNS), and non-smokers (NS). This study demonstrated how smoking influences the ability to control skin temperature, as the NS and SNS groups were able to increase their skin temperature, while the SS group not only did not have this ability, but also showed a slight decrease of skin temperature after the BF session. Grimsley therefore argues that smoking causes lower hand skin temperature due to vasoconstriction and hinders the ability to modulate it, influencing the results of BF sessions and other psychological treatments involving relaxation.</p>
<p>Although the reviews taken into consideration present limitations, both at the level of the included studies (for example: methodological limitations such as the lack of a control group, a sample consisting of few subjects or non-standardized clinical outcomes) and at the level of the reviews themselves (for example: a small number of studies included and a poor quality of the same), the results show that these alternative approaches constitute promising measures to help smokers to quit smoking, facilitating the modulation of the activity of the Central and Autonomic Nervous System. Similarly, the study by <xref ref-type="bibr" rid="ref184">Pandria et al. (2023)</xref> confirms what emerged from the reviews examined, demonstrating the effectiveness of an integrated BF&#x2009;+&#x2009;NF approach on the clinical, behavioral, and cognitive aspects of smokers. At present, it is not possible to determine whether this integrated approach produces better results than the two approaches applied individually, as there are no effect size measures either in the reviews considered or in the study by Pandria and collaborators. Furthermore, more studies, greater methodological rigor and follow-ups at multiple time intervals are needed to be able to carry out a precise analysis of the effectiveness of these techniques.</p>
<p>Recent studies have emphasized the importance &#x043E;f stress modulation techniques as crucial components &#x0456;n behavioral therapies, highlighting the potential &#x043E;f suicidal thoughts t&#x043E; temporarily reduce stress through the decrease &#x043E;f heart rate variability (HRV) and skin conductance response (SCR), as demonstrated by <xref ref-type="bibr" rid="ref154">Linehan et al. (2015)</xref>. This suggests a calming effect &#x043E;f dysfunctional covert actions (suicidal thoughts), raising significant questions about the efficacy &#x043E;f targeted therapeutic strategies, such as paced breathing taught &#x0456;n dialectical behavior therapy. However, &#x0456;t &#x0456;s critical t&#x043E; note that such techniques have traditionally been taught without the integration &#x043E;f BF/NF techniques, specifically mentioning the absence &#x043E;f a combined NF&#x2009;+&#x2009;BF approach. This observation opens new avenues for future research, suggesting that the integration &#x043E;f NF and BF could offer an innovative intervention strategy t&#x043E; enhance stress management and reduce the incidence &#x043E;f suicidal thoughts. Our current study identifies and highlights the need t&#x043E; further explore this hypothesis through methodologically rigorous studies, &#x0456;n order t&#x043E; assess the efficacy &#x043E;f an integrated therapeutic approach combining BF and NF t&#x043E; effectively address stress-related dysfunctions.</p>
</sec>
<sec id="sec10">
<label>5.2</label>
<title>Sports performance</title>
<p>In the sporting world, psychophysiology provides valid support for improving the performance aspects of an athlete, who often finds himself facing races and competitions. The evaluation of performance aspects is limited if these are considered exclusively or attesting to physiological and mental parameters. Mind and body are one, they appear as two sides of the same coin that interact in the various dynamic processes studied and explored in depth in the various interdisciplinary fields that have long sought to provide answers on the body&#x2013;mind combination (<xref ref-type="bibr" rid="ref30">Cacioppo et al., 2007</xref>). In recent years, the psychophysiological monitoring of this combination has grown exponentially, thanks to the growing awareness that athletes and coaches are continuously searching for alternative and innovative methodologies for enhancing physical and mental abilities that can be positively correlated with sports performance (<xref ref-type="bibr" rid="ref1007">Diotaiuti et al., 2021a</xref>,<xref ref-type="bibr" rid="ref1008">b</xref>, <xref ref-type="bibr" rid="ref1011">2023</xref>; <xref ref-type="bibr" rid="ref229">Sieka&#x0144;ska et al., 2021</xref>; <xref ref-type="bibr" rid="ref111">Hsieh et al., 2023</xref>). Athletes, having to manage the times and methods of execution of the technical/athletic gesture, look for programs and technologies that accurately and thoroughly improve their performance (<xref ref-type="bibr" rid="ref144">Lange-Smith et al., 2023</xref>). An example is given by sports such as archery or shooting where the management of arousal turns out to be a fundamental aspect for dealing with physiological and behavioral conditioning coming from internal and external responses which influence performance (<xref ref-type="bibr" rid="ref165">Marzbani et al., 2016</xref>; <xref ref-type="bibr" rid="ref171">Mikicin et al., 2018</xref>; <xref ref-type="bibr" rid="ref1009">Diotaiuti et al., 2021c</xref>).</p>
<p>The evolution of research has led to the identification of a way to monitor and intervene on these aspects: biofeedback and neurofeedback training. In the sports field, the first studies were conducted using biofeedback and date back to 1991, when Petruzzello and colleagues were the first to investigate the use of this technique in this area. At the beginning, the studies did not produce significant effects due to various problems, attributed by the researchers to exploratory interventions and the lack of preliminary knowledge of the basic levels of EEG, HR and respiration (<xref ref-type="bibr" rid="ref191">Petruzzello et al., 1991</xref>). Over the years, the exploratory and interventional phenomenon of BF has extended to new protocols, highlighting its real effectiveness in physiological processes such as heart rate variability and muscle tension. Training aimed at these aspects can increase the effects of personal awareness to reduce and control states of stress (<xref ref-type="bibr" rid="ref56">De Witte et al., 2019</xref>). A classic example is deep breathing used to lower the heart rate, inducing a state of relaxation during high-pressure moments in a competition (<xref ref-type="bibr" rid="ref212">Russo et al., 2017</xref>; <xref ref-type="bibr" rid="ref141">Lalanza et al., 2023</xref>). Over time, in addition to the BF technique, the application of NF has also begun to take hold in the field of sports performance, through which the athlete learns to modulate his own brain activity by trying to achieve the desired states associated with a greater control of attention during performance.</p>
<p>The research conducted using the NF has mainly focused on the study of athletes belonging to sports disciplines that require attention and concentration skills. In this regard, some authors have been able to verify the effectiveness of NF training on the brain activity of some golfers. Athletes were trained to self-regulate their brain functions, particularly theta waves of the medial frontal region associated with cognitive and attentional control (<xref ref-type="bibr" rid="ref33">Chen et al., 2022</xref>; <xref ref-type="bibr" rid="ref1005">Corrado et al., 2024</xref>). Recently, <xref ref-type="bibr" rid="ref213">Rydzik et al. (2023)</xref> highlighted that the effect of sports training is positively associated with the NF method which, if used by athletes during training, can lead to the control and improvement of psychophysiological aspects. However, the author himself does not hide the limitations of the research by inviting the production of further research aimed at verifying the effectiveness of other protocols that would lead to better results in sporting contexts and with individual athletes.</p>
<p>Despite the considerable presence of NF studies, there are many difficulties faced by researchers in verifying the effectiveness and reliability of the various types of training proposed in sport (<xref ref-type="bibr" rid="ref1006">Vernon, 2005</xref>).</p>
<p>In a recent review on the topic, <xref ref-type="bibr" rid="ref89">Gong et al. (2021)</xref> examined the experiences and points of view of practitioners carrying out NF training in sport. The authors have brought to light many controversies related to the technical aspects and application areas of the various NF protocols adopted. There are many studies conducted with BF and NF training, but little evidence has been shown on the effectiveness of combined scientific protocols. If integrated, neurofeedback and biofeedback can provide a valid contribution to the athlete&#x2019;s performance (<xref ref-type="bibr" rid="ref223">Shaw et al., 2012</xref>). By monitoring brain activity and physiological responses, athletes can learn to regulate their emotions, manage fatigue, and achieve an optimal state of performance (<xref ref-type="bibr" rid="ref63">Dupee et al., 2016</xref>). Other evidence has emerged in the rehabilitation field: NF and BF techniques can in fact also be used in rehabilitation from injuries. In this case, neurofeedback can help athletes retrain and recover brain functions affected by concussions or other traumatic brain injuries (<xref ref-type="bibr" rid="ref45">Conder and Conder, 2014</xref>). Furthermore, it has been seen how biofeedback can help monitor and manage physiological responses during rehabilitation exercises (<xref ref-type="bibr" rid="ref88">Giggins et al., 2013</xref>). This confirms the hypothesis according to which the combination of neurofeedback and biofeedback protocols can provide a valid contribution to the improvement of mental and physical states, even if they are carried out separately (<xref ref-type="bibr" rid="ref230">Sime, 2003</xref>). This approach is very close to the theory of Neural Synergy Systems, which explains brain functionality as a complex system, with multiple components and networks that work together to produce coherent and integrated behaviors. This theory supports the idea that the brain operates through the coordination and cooperation of different neural systems rather than individual isolated parts. In their studies conducted with clinical cases, <xref ref-type="bibr" rid="ref253">Thompson et al. (2010)</xref> confirmed the need to proceed with an integrated biofeedback and neurofeedback approach. Both draw from Porges&#x2019; Polyvagal Theory, which provides theoretical aspects to understand the role that some nervous pathways have in relation to the physiological and psychological responses connected to each other. It has been shown that BF can train individuals to vary heart rate, which is an indicator of vagal tone and overall autonomic flexibility (<xref ref-type="bibr" rid="ref116">Jimenez Morgan and Molina Mora, 2017</xref>; <xref ref-type="bibr" rid="ref174">Mosley and Laborde, 2022</xref>). Similarly, NF can lead to an improvement in vagal tone, providing individuals with strategies to self-regulate their brain waves and promoting emotional and social well-being (<xref ref-type="bibr" rid="ref260">Villamil et al., 2019</xref>). In our comprehensive review &#x043E;f biofeedback and neurofeedback applications, &#x0456;t &#x0456;s crucial t&#x043E; highlight the groundbreaking contributions &#x043E;f Michael and Lynda Thompson &#x0456;n the field. Thompson&#x2019;s research, which elucidates the correlation between the sensorimotor rhythm (SMR) envelope (and thus power) and the outbreath during heart rate variability (HRV) biofeedback, marks a significant advancement &#x0456;n our understanding &#x043E;f the physiological underpinnings &#x043E;f biofeedback interventions (<xref ref-type="bibr" rid="ref251">Thompson and Thompson, 2009</xref>). This correlation underscores the intricate relationship between neurological processes and respiratory patterns, offering novel insights into the design and optimization &#x043E;f biofeedback protocols for various therapeutic outcomes. The gap &#x0456;n the literature regarding studies that combine end-tidal carbon dioxide (etCO2) measurements with neurofeedback (NF) &#x0456;s noteworthy and points t&#x043E; an exciting frontier for research, exploring the intersections &#x043E;f respiratory, cardiovascular, and neurological biofeedback t&#x043E; deepen our understanding &#x043E;f physiological coherence and its implications for health and disease. Thompsons&#x2019; extensive work, incorporating electromyography (EMG) biofeedback as a consistent component &#x043E;f their interventions, has contributed t&#x043E; a more holistic approach t&#x043E; biofeedback therapy. Their integrative methodology, emphasizing the simultaneous application &#x043E;f neurofeedback and EMG biofeedback, has been instrumental &#x0456;n addressing complex clinical presentations (<xref ref-type="bibr" rid="ref252">Thompson and Thompson, 2023</xref>).</p>
<p>Given the connection and the aspects that the two interventions have in common, it would be reasonable to think that the combined use of the two protocols could produce better effects than their separate application. Most studies conducted in sports have used the two interventions separately (<xref ref-type="bibr" rid="ref208">Rijken et al., 2016</xref>).</p>
<p>In 2021, Shokri and collaborators compared the integrated BF&#x2009;+&#x2009;NF approach with BF alone on a sample of 45 novice basketball players. The authors randomized the sample into three intervention, two experimental, and one control groups. In the first experimental group the sample performed only 24 biofeedback sessions, while the second experimental group received a combination of neurofeedback and biofeedback. Athletes were monitored in four basic technical skills: lay-ups, chest passes, dribbling, and free throws. Participants in the combined intervention group showed significant improvement in all four core skills, while the biofeedback-only group showed improvements only in layup and passing performance. In each of the four skills measured, attention, reaction time, and vigilance play a decisive role so that, compared to the group that received only the BF, the level of performance was better in the group that received the intervention integrated, confirming its effectiveness. This improvement can be attributed to the changes produced in the brain by neurofeedback, which can lead to a concrete increase in attention and a reduction in reaction times (<xref ref-type="bibr" rid="ref228">Shokri and Nosratabadi, 2021</xref>).</p>
<p>The results of these two recent studies are clear and evident and show the effectiveness of the double intervention. Future research in sports should focus on protocols that include integrated intervention training. If in the past studies on sport have focused on a separate use of BF and NF, today the integrated approach can provide more possibilities for intervention, integrating multiple aspects to be strengthened. By providing both psychological and physiological training, concrete and effective results can be achieved.</p>
</sec>
<sec id="sec11">
<label>5.3</label>
<title>Attention deficit hyperactivity disorder</title>
<p>In recent decades, advances in neuroscience have led to a greater understanding of the functioning of the brain and its dysfunctions associated with disorders such as ADHD (<xref ref-type="bibr" rid="ref146">Leffa et al., 2022</xref>). Attention Deficit Hyperactivity Disorder (ADHD) is characterized by a pattern of inattention and/or hyperactivity-impulsivity that interferes with functioning or development. It is considered one of the most common psychiatric disorders in children and adolescents (<xref ref-type="bibr" rid="ref74">Fawns, 2021</xref>) and leads to problems in school, impaired social skills and poorer adaptive functioning in major life activities (<xref ref-type="bibr" rid="ref86">Gevensleben et al., 2009</xref>). ADHD causes cognitive deficits especially in reference to executive functions, which allow the production of behaviors aimed at achieving a specific goal (<xref ref-type="bibr" rid="ref164">Mart&#x00ED;nez et al., 2016</xref>) and is also characterized by excessive sensitivity to reinforcements, which corresponds to a difficulty in waiting for gratification. One of the executive functions most affected in ADHD is inhibitory control, that is, the inability to inhibit irrelevant responses (<xref ref-type="bibr" rid="ref11">Barkley, 2022</xref>). People with ADHD have slower response times during cognitive tasks (<xref ref-type="bibr" rid="ref224">Shen et al., 2011</xref>). The inhibitory deficit is associated with both structural and functional anomalies in the frontostriatal and frontoparietal circuits, highlighting hypoactivation in &#x201C;go/no go&#x201D; type tasks compared to the normal population (<xref ref-type="bibr" rid="ref55">De La Fuente et al., 2013</xref>; <xref ref-type="bibr" rid="ref106">Hart et al., 2013</xref>). The disorder also consists of considerable difficulties in the modulation of affective states, due to alterations in motor control (<xref ref-type="bibr" rid="ref232">Sobanski et al., 2010</xref>), and in the recognition and understanding of emotional information and all this often translates into aggression, irritability, or frustration (<xref ref-type="bibr" rid="ref162">Martel and Nigg, 2006</xref>). For this reason, various pharmacological, cognitive-behavioral, and family treatments are recommended (<xref ref-type="bibr" rid="ref247">Taylor et al., 2004</xref>). However, cognitive-behavioral intervention strategies have not always proven effective, especially with regard to generalization and long-term effects (<xref ref-type="bibr" rid="ref47">Cortese et al., 2015</xref>; <xref ref-type="bibr" rid="ref72">Evans et al., 2018</xref>). Therefore, we tried to find other effective strategies in improving the attention and self-management skills of patients suffering from ADHD.</p>
<p>Research on the rhythms of brain electrical activity in various frequency bands highlights that anatomically complex homeostatic systems regulate the power spectrum of the EEG. Cortical, thalamic, and brainstem processes mediate this regulation through major neurotransmitters, so a deficiency or excess of any neurotransmitter can produce a change in the EEG spectrum and contribute to psychiatric pathophysiology (<xref ref-type="bibr" rid="ref43">Coburn et al., 2006</xref>). Conditions such as epilepsy, anxiety disorder, depression, dementia, obsessive-compulsive disorder, schizophrenia, learning disability, and ADHD present abnormal patterns in brain electrical activity (<xref ref-type="bibr" rid="ref198">Popa et al., 2020</xref>). The presence of an excessive amount of slow waves in the frontal areas of the brain leads to difficulty in controlling attention, behavior, and emotions. In this case, people usually present problems with concentration, memory, impulse control, and hyperactivity, along with dysfunctions in focus and intellectual efficiency (<xref ref-type="bibr" rid="ref103">Hammond, 2011</xref>). The discovery of alterations in the rhythms of brain electrical activity has led to the demonstration that these rhythms play an important role in the maintenance of brain function and, consequently, can be used in the diagnosis of brain dysfunction (<xref ref-type="bibr" rid="ref26">Britton et al., 2016</xref>). Furthermore, as previously highlighted, the ability to modify specific patterns of brain activity leads to the possibility of using other therapies or alternative treatments, such as neurofeedback (<xref ref-type="bibr" rid="ref231">Sitaram et al., 2017</xref>).</p>
<p>The main goal of neurofeedback in the treatment of ADHD is to help the brain regulate activity in neural circuits responsible for attention and self-control (<xref ref-type="bibr" rid="ref68">Enriquez-Geppert et al., 2019</xref>), encouraging a reduction in their activity dysfunctional and promoting the activation of regions related to calm and concentration (<xref ref-type="bibr" rid="ref252">Thompson and Thompson, 2023</xref>). Over the past 5&#x2009;years, studies using neurofeedback have reported consistent small to medium sized effects in symptom improvement. In 2019, Enriquez-Geppert and collaborators provided an overview of the use of NF in the treatment of ADHD, examining the scientific evidence on its effectiveness and clinical implementations. Based on meta-analysis studies, three standard NF protocols (theta/beta, sensorimotor rhythm, and slow cortical potential) have been identified that have proven effective in the treatment of ADHD. However, there are currently no uniform treatment standards in the clinical setting. This leads to the need to regulate NF as a therapy and to have application standards at an international level. The same authors noted that thanks to NF a patient can reduce symptoms of impulsivity and improve concentration, successfully interrupting drug therapy (<xref ref-type="bibr" rid="ref68">Enriquez-Geppert et al., 2019</xref>). However, pharmacological therapy remains a fixed and essential point for treating the symptoms of ADHD. In the same year, other authors conducted a systematic review with the aim of comparing the efficacy and tolerability of methylphenidate (MPH) and NF as treatments for ADHD. The results showed that the two treatments do not show any difference, although this conclusion is not unanimously accepted (<xref ref-type="bibr" rid="ref1011">Yan et al., 2019</xref>). A 2022 study investigated the potential additional effects of NF when combined with drug therapy, finding that NF combined with medications shows positive effects on global ADHD symptomatology and inattention symptoms, even if the effects do not persist for more than 6&#x2009;months after treatment. Overall, the findings support the idea that supplementing NF with medications provides additional benefits in the treatment of global and inattention symptoms in ADHD patients (<xref ref-type="bibr" rid="ref153">Lin et al., 2022</xref>).</p>
<p>In 2021, Baena and colleagues investigated the effectiveness of NF interventions in children with ADHD and showed the utility of NF in improving ADHD symptomatology in children through learning appropriate video training (<xref ref-type="bibr" rid="ref158">Luo et al., 2023</xref>). NF has been shown to have positive and long-lasting effects on ADHD symptoms, significantly improving behavior, attention, IQ and reaction times, with related benefits in motor control and bimanual coordination, which are often problematic in children with ADHD (<xref ref-type="bibr" rid="ref1012">Sampedro Baena et al., 2021</xref>). In a further meta-analysis, some authors examined the efficacy of NF in the treatment of core symptoms of ADHD, highlighting significant improvements in symptoms of inattention and hyperactivity/impulsivity and in global symptoms of ADHD, which appear to be associated with a reduction in theta waves (<xref ref-type="bibr" rid="ref82">Fullen et al., 2020</xref>). However, according to some authors, NF remains a controversial approach, arguing that it is a purely experimental method that cannot be considered valid for ADHD. In fact, although many studies on NF have reported positive effects, <xref ref-type="bibr" rid="ref270">Zilverstand et al. (2017)</xref> highlighted conflicting results, finding positive effects only on cognitive functioning. Neurofeedback intervention aimed at reducing the theta/beta ratio represents the main choice for the treatment of ADHD (<xref ref-type="bibr" rid="ref258">Van Doren et al., 2017</xref>). However, its results have not been fully proven (<xref ref-type="bibr" rid="ref180">Neuh&#x00E4;u&#x00DF;er et al., 2023</xref>). The presence of individual variations in EEG tracings could explain this ineffectiveness (<xref ref-type="bibr" rid="ref23">Bluschke et al., 2016</xref>). In fact, it has been seen how the alpha rhythm (which plays an important role in the cognitive, psychomotor, psychoemotional, and physiological functions of the brain) could be mistakenly considered as high theta activity according to the normal frequency ranges (<xref ref-type="bibr" rid="ref69">Escolano et al., 2014</xref>). This has led to evidence that children with ADHD have a higher theta/alpha ratio, in addition to the theta/beta ratio (<xref ref-type="bibr" rid="ref114">Janssen et al., 2020</xref>). NF targeting theta/beta ratio could negatively affect alpha activity if frequency bands are not identified correctly. Therefore, it is important to track individual frequency bands based on peak frequency and alpha band width. Furthermore, it has emerged that individual variability in the EEG can influence irrelevant areas of the brain if not taken into account (<xref ref-type="bibr" rid="ref159">MacDonald et al., 2009</xref>) and this could have a negative impact on ADHD-related activities, risking worsening symptoms instead of improving them.</p>
<p>Recent studies have highlighted that, although a significant subgroup &#x043E;f individuals with ADHD exhibit patterns &#x043E;f hypoactivation, there &#x0456;s also a pattern &#x043E;f hyperactivation &#x0456;n other cases. This diversity &#x0456;n activation patterns has been linked t&#x043E; variability &#x0456;n responses t&#x043E; pharmacological treatments, such as the alpha channel blocker guanfacine and the differences &#x0456;n the effectiveness &#x043E;f dopamine vs. noradrenaline reuptake inhibitors. Research conducted by <xref ref-type="bibr" rid="ref37">Clark et al. (2022)</xref>, <xref ref-type="bibr" rid="ref8">Arns et al. (2020)</xref>, as well as <xref ref-type="bibr" rid="ref136">Kropotov (2020)</xref>, has demonstrated these differences &#x0456;n EEG patterns, suggesting that the hypoactivation hypothesis cannot be universally applied t&#x043E; all individuals with ADHD. This variability underscores the importance &#x043E;f considering a personalized approach &#x0456;n the diagnosis and treatment &#x043E;f ADHD, taking into account the specific neurophysiological characteristics &#x043E;f the individual. In addition t&#x043E; the discussion &#x043E;n the effect &#x043E;f an excessive amount &#x043E;f slow waves &#x0456;n the frontal area compromising control, recent studies, such as those conducted by <xref ref-type="bibr" rid="ref37">Clark et al. (2022)</xref>, have highlighted how an excessive presence &#x043E;f fast waves, specifically the &#x201C;beta-spindling&#x201D; phenomenon, can have a similar impact. This evidence broadens our understanding &#x043E;f how specific variations &#x0456;n brain activity patterns can influence cognitive and behavioral control. The elevated presence &#x043E;f beta activity, associated with states &#x043E;f anxiety, hyper-vigilance, &#x043E;r stress, suggests that both slow and fast oscillations must be considered &#x0456;n assessing brain functionality and designing therapeutic interventions. Therefore, &#x0456;n our study, we have included a more comprehensive assessment &#x043E;f brain activity patterns, recognizing that both hypoactivation and hyperactivation can contribute t&#x043E; behavioral and cognitive dysfunctions &#x0456;n various clinical conditions.</p>
<p>Some authors suggest that NF causes non-specific effects, improving concentration, self-efficacy and the ability to sit still in children, but these changes may not only be due to cortical regulation, but also to other factors such as breathing or eye movements (<xref ref-type="bibr" rid="ref124">Karjalainen et al., 2023</xref>). To establish the specific efficacy of cortical regulation in NF it is important to use adequate controls. A common control modality is &#x201C;sham neurofeedback,&#x201D; which provides non-specific or non-real signals to a control group in order to determine whether the changes observed in the experimental group are attributable to the effects of real NF (<xref ref-type="bibr" rid="ref217">Sch&#x00F6;nenberg et al., 2017</xref>). However, the use of fake NF can lead to methodological difficulties and ethical concerns, as it involves the administration of fake feedback to children with ADHD who in this way, despite having contributed to the experimental project, were not able to derive any benefits from the treatment.</p>
<p>In addition &#x043E;n the methodological critique &#x043E;f neurofeedback (NF), &#x0456;t &#x0456;s imperative t&#x043E; consider the analogy between sham controls &#x0456;n NF research and placebo controls &#x0456;n medication studies. Recent discussions, as highlighted by studies such as those by <xref ref-type="bibr" rid="ref160">Maneeton et al. (2015)</xref> have emphasized the substantial effects &#x043E;f placebos &#x0456;n medication trials. This &#x0456;s particularly relevant when comparing the efficacy &#x043E;f medications like methylphenidate (MPH) against placebo, where the difference, albeit significant, also underscores the non-negligible impact &#x043E;f placebo itself. Considering this, we propose a nuanced exploration &#x043E;f the placebo effect &#x0456;n medication trials relative t&#x043E; sham NF controls. This involves questioning whether the baseline t&#x043E; post-treatment placebo effect &#x0456;s indeed smaller than the interaction effect observed &#x0456;n comparisons like MPH(t1&#x2009;&#x2212;&#x2009;t2)&#x2009;&#x2212;&#x2009;Placebo(t1&#x2009;&#x2212;&#x2009;t2). Such an inquiry &#x0456;s not only pivotal for understanding the magnitude &#x043E;f placebo effects but also for appreciating the complexity &#x043E;f interpreting NF efficacy against these backgrounds. This approach underscores the importance &#x043E;f rigorous, comparative study designs &#x0456;n elucidating the true value &#x043E;f NF &#x0456;n contrast to, and potentially &#x0456;n combination with, traditional pharmacological treatments.</p>
<p>We acknowledge that, alongside our discourse &#x043E;n ADHD and the T/B (Theta/Beta) methodology, &#x0456;t &#x0456;s critical t&#x043E; incorporate an analysis &#x043E;f Slow Cortical Potentials (SCP, according t&#x043E; <xref ref-type="bibr" rid="ref21">Birbaumer, 1999</xref>) and Infra-Low Frequency (ILF). SCPs offer EMG control via the oculogram, essential for ADHD clients during specific parts &#x043E;f the training that require EEG control, such as during the 8-s phase &#x043E;f the SCPs, making &#x0456;t difficult for ADHD clients not t&#x043E; blink. Studies like those by <xref ref-type="bibr" rid="ref238">Strehl et al. (2017)</xref> have demonstrated the effectiveness &#x043E;f EMG as a control group, highlighting that even &#x0456;n methodologies that include EMG control, the training could be beneficial. Moreover, the integration &#x043E;f ILF, as discussed &#x0456;n special editions &#x043E;f Frontiers, adds an additional layer &#x043E;f complexity and potential efficacy t&#x043E; the treatment &#x043E;f ADHD, offering a deeper understanding and new avenues for therapeutic intervention. Regarding medication, &#x0456;t &#x0456;s known that many children d&#x043E; not tolerate Methylphenidate (MPH) due t&#x043E; side effects such as premature graying, insomnia, and psychotic symptoms. If Theta/Beta Neurofeedback training proves t&#x043E; be as effective as MPH without these side effects, patients should be informed &#x043E;f the existence &#x043E;f this therapeutic alternative.</p>
<p>An alternative to NF could be the use of electromyographic BF (EMG-BF), which targets motor control rather than regulation of cortical activity. This method could represent a type of control suitable for investigating the specificity of the effects of NF. It was noted that the electromyogenic (EMG) signal generated by the forehead muscles could explain the poor efficacy of NF in ADHD. Elevated forehead muscle tone is considered a sign of psychoemotional tension or mental stress, which may be present in ADHD, and this has led to the hypothesis that the effectiveness of NF treatment may further increase if combined with a practice of EMG-BF (<xref ref-type="bibr" rid="ref12">Barth et al., 2017</xref>).</p>
<p>In 2013, some authors attempted to demonstrate a differential EMG-BF training method for children with ADHD through the use of different NF training protocols. This method was designed as control training. EMG-BF was used to monitor the activity of arm muscles involved in fine motor skills, such as writing and grip strength control. The authors managed to demonstrate improvements in motor regulation in various task conditions, achieving a significant reduction in behavioral symptoms related to ADHD. The differential EMG-BF approach is found to be useful and provides adequate control conditions for NF training in ADHD research (<xref ref-type="bibr" rid="ref168">Maurizio et al., 2013</xref>). In 2011, some authors put forward the idea of comparing two types of training to evaluate the effects on the primary symptoms of ADHD: NF to reduce the theta/beta ratio and EMG-BF aimed at relaxing the frontal muscles. For this study, 35 children with ADHD were randomly assigned to the NF group (18 participants) and the BF control group (17 participants). Both groups received 30 treatment sessions. The results showed that the NF group effectively reduced theta/beta ratios and EMG level, and BF achieved a positive impact similar to NF. The study demonstrated that NF is effective in reducing symptoms of inattention in children with ADHD, but suggests that other factors may also influence symptom improvements (<xref ref-type="bibr" rid="ref10">Bakhshayesh et al., 2011</xref>).</p>
<p><xref ref-type="bibr" rid="ref15">Bazanova et al. (2018)</xref> conducted a study to evaluate the effectiveness of a personalized NF intervention based on the theta/beta ratio by combining it with the frontal EMG-BF protocol, in order to treat 94 children with ADHD aged between 6 and 9&#x2009;years. The experimental design involved randomly dividing participants into four groups in order to reduce the theta/beta ratio (TBR): standard NFT group (sNFT; <italic>n</italic>&#x2009;=&#x2009;17) with standard frequency bands (4&#x2013;8&#x2009;Hz for theta and 12, 5&#x2013;20&#x2009;Hz for beta); individual neurofeedback training group (iNFT; <italic>n</italic>&#x2009;=&#x2009;31), in which theta and beta target frequency bands were individually adapted for each participant; individual NFT group with simultaneous EMG (iNFT_EMG; <italic>n</italic>&#x2009;=&#x2009;32) where participants received a customized NFT with targeted adjustments to frequency bands and integrated frontalis muscle EMG power to reduce muscle tension; placebo group (sham NF).</p>
<p>The researchers followed a conventional Neurofeedback Training (NFT) protocol to address attention deficit hyperactivity disorder (ADHD) by reducing Theta-beta ratio (TBR) levels, referring to work of <xref ref-type="bibr" rid="ref173">Monastra (2005)</xref>. In this case, the participants underwent 10 sessions of NF each lasting 16&#x2009;min with their eyes open. During these training sessions, participants sitting in front of a computer monitor and tasked with modulating their TBR were encouraged to develop a mental strategy to reduce their TBR.</p>
<p>The reward criteria were set such that TBR values exceeded a certain threshold in the respective groups. The threshold calculation varied as follows: For the sNFT group, the threshold was based on the average standard frequency power (4&#x2013;8&#x2009;Hz for theta and 12&#x2013;15&#x2009;Hz for beta). For the iNFT and iNFT_EMG groups, the thresholds were based on the average power of the individually adjusted frequency ranges, while in the iNFT_EMG group the average power of the integrated frontal EMG was considered. In this case the feedback signal appeared only when both the TBR and EMG signals fell below their respective thresholds.</p>
<p>The results of the study confirmed most of the findings on the electrophysiological profile of ADHD, demonstrating a capacity of alpha and beta powers, as well as a leftward shift of the peak frequency of the individual alpha wave in ADHD compared to the control group. Furthermore, it has been shown that personalized NF is more effective in improving attention and impulse control in children with ADHD than the standard protocol and that the effect is more long-lasting when combined with simultaneous EMG control. In conclusion, the effectiveness of NF can be increased by taking into account individual characteristics of EEG and muscle tension (<xref ref-type="bibr" rid="ref15">Bazanova et al., 2018</xref>).</p>
<p>Research has shown that individuals with ADHD exhibit differences in specific measures of HRV (<xref ref-type="bibr" rid="ref222">Shaffer et al., 2014</xref>). It has been seen that heart rate variability can provide important information on sustained attention and disturbances in emotional and behavioral regulation observed in ADHD (<xref ref-type="bibr" rid="ref93">Griffiths et al., 2017</xref>). HRV is a therapeutic approach that aims to train individuals to control a specific aspect of HRV known as respiratory sinus arrhythmia (RSA) (<xref ref-type="bibr" rid="ref149">Lehrer and Gevirtz, 2014</xref>). The goal of this intervention is to increase heart rate variability leading to positive effects on psychological well-being, such as the reduction of stress and symptoms of anxiety, depression, and post-traumatic stress disorder (PTSD; <xref ref-type="bibr" rid="ref87">Gevirtz, 2013</xref>). <xref ref-type="bibr" rid="ref156">Lloyd et al. (2010)</xref> subjected children with ADHD to HRV training and showed that this treatment helps reduce several behavioral symptoms of ADHD, providing a promising non-pharmacological treatment strategy for individuals with this condition.</p>
<p>In conclusion, ADHD is a disorder characterized by symptoms that can affect the daily functioning of individuals who suffer from it. Traditional interventions, such as drug treatment and cognitive-behavioral therapy, can be effective but have limitations, including side effects of medications and uncertain long-term outcomes for behavioral therapies. Despite some methodological controversies, NF represents a promising therapeutic option for the treatment of ADHD, with the possibility of reducing drug dependency and improving patients&#x2019; quality of life. The demonstration is given by the fact that Neurofeedback, in particular that aimed at reducing the theta/beta ratio, can have positive effects on the symptoms of ADHD. However, there are individual variations in EEG tracings that can influence the effectiveness of the treatment. For this reason it is important to consider individual factors when designing neurofeedback training. Combining neurofeedback with electromyographic biofeedback (EMG-BF) targeting muscle control may further improve outcomes in the treatment of ADHD. This combination appears to have positive effects on the global symptomatology of ADHD and on the reduction of frontal muscle tension. Despite the positive effects observed, there is a need to regulate neurofeedback as a valid therapy for ADHD and establish application standards internationally to ensure consistent and reliable results.</p>
</sec>
<sec id="sec12">
<label>5.4</label>
<title>Autism</title>
<p>Autism Spectrum Disorder (ASD) is an early-onset neurodevelopmental disorder characterized by difficulties in social interaction and communication, restricted interests and repetitive and stereotyped behaviors, and deficits in executive functions and emotional regulation (<xref ref-type="bibr" rid="ref5">APA, 2013</xref>). The latest revision of the Statistical and Diagnostic Manual of Mental Disorders, the DSM-5 (<xref ref-type="bibr" rid="ref5">APA, 2013</xref>), has modified the diagnostic classification of this pathology by introducing the concept of &#x201C;autism spectrum&#x201D; (which includes four independent diagnoses from the previous DSM-IV: autistic disorder, Asperger syndrome, pervasive developmental disorder not otherwise specified and childhood disintegrative disorder) and moving from a categorical diagnosis typical of previous versions of the manual to a dimensional diagnosis, in which the level of severity of the symptoms, or of general clinical problem, takes on a central role in the diagnostic process. Therefore, each characteristic, symptom or deficit is defined along a continuum within which intensity and severity can be placed. From a neurobiological point of view, ASD is characterized by impairments in some brain regions, such as the amygdala and the facial fusiform area (<xref ref-type="bibr" rid="ref3">Adolphs et al., 2001</xref>; <xref ref-type="bibr" rid="ref218">Schultz et al., 2003</xref>), and by alterations in connectivity functional within and between brain networks, such as the Default Mode Network, the Salience Network, the Executive Control Network, and the Mirror Neuron System (<xref ref-type="bibr" rid="ref127">Kennedy et al., 2006</xref>; <xref ref-type="bibr" rid="ref257">Uddin and Menon, 2009</xref>; <xref ref-type="bibr" rid="ref227">Shih et al., 2010</xref>; <xref ref-type="bibr" rid="ref77">Fishman et al., 2014</xref>). These anomalous connectivity patterns may underlie the disorganized and dysfunctional integration of information that characterizes individuals with ASD (<xref ref-type="bibr" rid="ref27">Brock et al., 2002</xref>; <xref ref-type="bibr" rid="ref16">Belmonte et al., 2004</xref>).</p>
<p>In addressing the critical insights into neurofeedback (NF) applications within Autism Spectrum Disorder (ASD), &#x0456;t &#x0456;s imperative t&#x043E; acknowledge the pioneering work &#x043E;f Robert Coben. His research has significantly contributed t&#x043E; our understanding &#x043E;f the neural underpinnings &#x043E;f ASD, particularly regarding the patterns &#x043E;f over and underconnectivity observed &#x0456;n individuals with ASD (<xref ref-type="bibr" rid="ref40">Coben et al., 2008</xref>, <xref ref-type="bibr" rid="ref41">2010</xref>; <xref ref-type="bibr" rid="ref42">Coben and Myers, 2008</xref>). Coben&#x2019;s work has elucidated the complex neural connectivity issues that characterize ASD, highlighting the potential for targeted neurofeedback interventions t&#x043E; ameliorate these specific neural discrepancies. Coben&#x2019;s innovative approach t&#x043E; coherence neurofeedback distinguishes his work within the field. Coherence neurofeedback, focusing &#x043E;n the synchronization between different regions &#x043E;f the brain, has shown promising results &#x0456;n improving the symptoms &#x043E;f ASD, including social interaction, communication, and behavioral flexibility. Coben&#x2019;s methodology involves the careful assessment and modulation &#x043E;f brain connectivity, offering a tailored therapeutic intervention that addresses the unique neurophysiological profile &#x043E;f each individual with ASD.</p>
<p>At a non-central level, however, attention has begun to be paid to the role that the Peripheral Nervous System (PNS) plays in this pathology. According to Polyvagal Theory of <xref ref-type="bibr" rid="ref199">Porges (2001</xref>, <xref ref-type="bibr" rid="ref200">2003</xref>, <xref ref-type="bibr" rid="ref201">2007)</xref>, the vagus nerve is a mediator of social behavior and, therefore, its dysfunction may contribute to social disorders such as autism. The vagus nerve contributes to the regulation of the Autonomic Nervous System (ANS) through connections with the heart and other visceral organs and is involved in the Social Engagement System (which includes a series of elements related to sociality, such as gaze, facial expression, prosody, etc.), so it is thought that its malfunction could mediate the social avoidance behaviors typical of ASD.</p>
<p>Given the importance attributed to the Central Nervous System (CNS) and the Peripheral Nervous System in the typical dysfunctions of ASD, <xref ref-type="bibr" rid="ref90">Goodman et al. (2018)</xref> conducted a study aimed at intervening on both top-down (CNS) and bottom-up processes -up (SNP) in order to evaluate its effectiveness in improving ASD symptoms. Specifically, the aim of their study was 2-fold: to evaluate the effect of a BF intervention using HRV (HRV-BF) on ASD symptoms and to examine whether a combination of HRV-BF and NF targeted the Mu rhythm (MRS-NF) was more effective than HRV-BF applied individually. The Mu rhythm was chosen as the target of NF training as it is linked to the activity of the Mirror Neuron System and, therefore, implicated in social and imitation behaviors (<xref ref-type="bibr" rid="ref193">Pineda, 2008</xref>; <xref ref-type="bibr" rid="ref19">Bernier et al., 2013</xref>; <xref ref-type="bibr" rid="ref24">Braadbaart et al., 2013</xref>), compromises in subjects suffering from ASD. Training this brain wave has shown promise in reducing linguistic symptoms and deficits in social cognition and emotional responsivity (<xref ref-type="bibr" rid="ref194">Pineda et al., 2008</xref>, <xref ref-type="bibr" rid="ref195">2014a</xref>; <xref ref-type="bibr" rid="ref80">Friedrich et al., 2015</xref>). HRV training was instead chosen as it could reflect social behavior based on the principle of neurovisceral integration (<xref ref-type="bibr" rid="ref250">Thayer and Lane, 2000</xref>). It is not only the CNS that influences the activity of the ANS through efferent connections mediated by the vagus nerve, but also the visceral regions send afferent information to the brain areas. This bidirectional system is known as the Central Autonomic Network (<xref ref-type="bibr" rid="ref17">Benarroch, 1993</xref>) and some regions of this network (such as the amygdala, the insula and the anterior cingulate and orbitofrontal cortices) overlap with networks involved in attentional, emotional and social processing which play a role in ASD (<xref ref-type="bibr" rid="ref214">Sabbagh, 2004</xref>; <xref ref-type="bibr" rid="ref121">Kana et al., 2007</xref>; <xref ref-type="bibr" rid="ref59">Di Martino et al., 2009</xref>; <xref ref-type="bibr" rid="ref257">Uddin and Menon, 2009</xref>). This system maintains the homeostatic balance between the CNS and the PNS, therefore HRV training not only acts on the PNS, but also influences the activity of the CNS.</p>
<p>The sample of the study by <xref ref-type="bibr" rid="ref90">Goodman et al. (2018)</xref> consisted of 15 children diagnosed with ASD divided into two groups: Group 1 underwent HRV-BF training, while Group 2 underwent HRV-BF&#x2009;+&#x2009;MRS-NF training. All children underwent a pre-test phase (T1) consisting of qEEG, Mu rhythm suppression index, baseline HRV, Social Responsiveness Scale-2 (<xref ref-type="bibr" rid="ref46">Constantino, 2012</xref>), Emotion Regulation Checklist (<xref ref-type="bibr" rid="ref226">Shields and Cicchetti, 1997</xref>), Spence Children&#x2019;s Anxiety Scale (<xref ref-type="bibr" rid="ref234">Spence, 1998</xref>; <xref ref-type="bibr" rid="ref179">Nauta et al., 2004</xref>), and Autism Treatment Evaluation Checklist (<xref ref-type="bibr" rid="ref209">Rimland and Edelson, 1999</xref>). They were subsequently subjected to diagnostic tests and four preliminary sessions of HRV-BF. Group 1 was then given an additional 12&#x2009;h of HRV-BF (in which children were reinforced for breathing at their resonant rate, while punished for breathing faster), while Group 2 was given 12&#x2009;h of HRV-BF&#x2009;+&#x2009;MRS-NF in which, not only were children reinforced and punished for breathing at their resonant frequency, but they were also reinforced when they increased Mu rhythm levels and punished when they decreased them. Finally, all children underwent a post-test phase similar to the pre-test phase (T2).</p>
<p>The results of this study showed no differences between groups over time in social behavior, autistic symptoms, emotion regulation, anxiety, or HRV. However, Group 1 showed significant improvements in emotional regulation (&#x014B;<sup>2</sup>&#x2009;=&#x2009;0.511) and social behavior (&#x014B;<sup>2</sup>&#x2009;=&#x2009;0.730), while in Group 2 significant improvements occurred in emotional negativity/lability (&#x014B;<sup>2</sup>&#x2009;=&#x2009;0.461), autistic symptoms (&#x014B;<sup>2</sup>&#x2009;=&#x2009;0.499) and in HRV (&#x014B;<sup>2</sup>&#x2009;=&#x2009;0.226). Furthermore, significant time&#x2009;&#x00D7;&#x2009;group differences (&#x014B;<sup>2</sup>&#x2009;=&#x2009;0.364) were found in Mu rhythm suppression according to a pattern contrary to what the authors hypothesized: Group 1 showed a small increase in Mu rhythm suppression, while Group 2 did there is a large reduction in the suppression of this rhythm (i.e., a less adaptive response). In this study, the effect of MRS-NF on Mu rhythm suppression contrasts with what was observed previously in the literature (<xref ref-type="bibr" rid="ref192">Pineda, 2005</xref>; <xref ref-type="bibr" rid="ref194">Pineda et al., 2008</xref>, <xref ref-type="bibr" rid="ref196">2014b</xref>; <xref ref-type="bibr" rid="ref80">Friedrich et al., 2015</xref>) and this could be due to several reasons. For example, the ability to suppress the Mu rhythm may require a longer training period than allowed in the study by Goodman and colleagues (<xref ref-type="bibr" rid="ref194">Pineda et al., 2008</xref>; <xref ref-type="bibr" rid="ref80">Friedrich et al., 2015</xref>). A second possibility is that synergistic alpha synchronization occurred in the HRV-BF&#x2009;+&#x2009;MRS-NF group, as slow breathing may induce a higher alpha rhythm due to relaxation (<xref ref-type="bibr" rid="ref32">Casciaro et al., 2013</xref>). Another explanation could be that the training protocol used did not actually provide a reward and, finally, it is possible that the results were distorted by the poorness of the EEG signal or the presence of artifacts during data collection. Regarding HRV-BF, the study by Goodman and colleagues was the first to suggest that this technique can positively influence the symptoms of ASD, as shown by the results obtained from Group 1. However, due to the small number of participants and the lack of a control group, the results obtained by both groups cannot be generalized to the reference population.</p>
<p>Since there are no systematic reviews in the literature relating to the effectiveness of BF training in improving the symptoms of ASD, we will limit ourselves to comparing only the results of MRS-NF training obtained by <xref ref-type="bibr" rid="ref90">Goodman et al. (2018)</xref> with those reported in the only systematic review to have taken into consideration studies conducted with the NF technique on subjects suffering from ASD, in order to confirm or refute its effectiveness. <xref ref-type="bibr" rid="ref139">Kumari and Sharma&#x2019;s (2020)</xref> review includes 17 studies that used NF training to improve social cognition deficits in ASD. However, only five studies used the Mu rhythm-targeted protocol. Of these, the study by <xref ref-type="bibr" rid="ref195">Pineda et al. (2014a)</xref> showed improvements in social/cognitive awareness and communication, the study by <xref ref-type="bibr" rid="ref54">Datko et al. (2018)</xref> highlighted positive changes in communication, the studies by <xref ref-type="bibr" rid="ref194">Pineda et al. (2008)</xref> detected changes in social/cognitive awareness and imitation and the 2015 study by Friedrich and colleagues demonstrated improvements in communication and imitation. Unfortunately, however, due to the heterogeneity of the studies in terms of design, follow-up and presentation of details, Kumari and Sharma were unable to conduct a quantitative pre-post training analysis, so there are no effect size measures that provide robustness to the results obtained, thus not allowing precise conclusions to be drawn. In our literature search we found two other reviews that dealt with the topic of NF in relation to ASD, but they were not included in our work for two reasons. First, in the review by <xref ref-type="bibr" rid="ref207">Ribas et al. (2022)</xref>, the NF interventions were different from the one examined in our review (i.e., the MRS-NFB) and, secondly, although in the work of <xref ref-type="bibr" rid="ref112">Hurt et al. (2014)</xref> there were four studies based on NF training, only two had used the protocol targeting the Mu rhythm (<xref ref-type="bibr" rid="ref194">Pineda et al., 2008</xref>) and they were both already mentioned in the 2020 review by Kumari and Sharma cited previously.</p>
<p>In conclusion, by comparing the results obtained by <xref ref-type="bibr" rid="ref90">Goodman et al. (2018)</xref> with those highlighted by the review by <xref ref-type="bibr" rid="ref139">Kumari and Sharma (2020)</xref>, it is possible to highlight, although not in a rigorous manner, the ability of an MRS-NF intervention to bring about improvements in various aspects of social cognition in individuals with ASD, such as communication, imitation, social/cognitive awareness, and social behavior. However, as previously mentioned, these results cannot be generalized and should be interpreted with caution due to both the small number of studies present in the literature and the methodological limitations they present. Further research characterized by greater methodological rigor (randomization, follow-up, presence of a control group, description of the sample and the procedure and clear explanation of the statistical analysis carried out and the results obtained) are therefore necessary to better understand the potential that a NF intervention has in improving the deficits in social cognition that characterize subjects affected by ASD. Similarly, based on the results obtained by <xref ref-type="bibr" rid="ref90">Goodman et al. (2018)</xref> and in consideration of the existing interconnection between CNS and ANS, future studies could deepen the use of vagal stimulation training via HRV-BF in order to verify its effectiveness on the social cognition deficits typical of ASD. If the effectiveness of this technique were to be confirmed, it could be used in joint NF&#x2009;+&#x2009;BF experiments, with the aim of establishing its validity and advantages compared to individual approaches applied individually.</p>
</sec>
</sec>
<sec id="sec13">
<label>6</label>
<title>Conclusion and future perspectives</title>
<p>Our discussion synthesizes the new insights garnered from the review, emphasizing the implications for both theory and practice. We delineate the unique contributions &#x043E;f integrating BF and NF, including the identification &#x043E;f specific conditions and settings where this approach yields significant benefits. By comparing our findings with existing literature, we spotlight gaps that our review addresses, such as the potential for personalized therapy protocols and the exploration &#x043E;f combined biofeedback modalities &#x0456;n diverse populations. Furthermore, we propose a framework for future investigations, underlining the necessity for robust, innovative studies t&#x043E; fully unravel the complexities &#x043E;f biological feedback. Ultimately, our review not only sheds light &#x043E;n previously uncharted territories but also sets the stage for transformative research &#x0456;n the field.</p>
<p>While &#x0456;t &#x0456;s true that the limited number &#x043E;f studies and the absence &#x043E;f detailed statistical data, such as effect size measures, necessitate caution &#x0456;n interpreting the results, this does not entirely preclude the possibility &#x043E;f drawing meaningful preliminary conclusions. Our review, despite highlighting these limitations, aims t&#x043E; emphasize the potential &#x043E;f the integrated BF&#x2009;+&#x2009;NF approach &#x0456;n improving various conditions and performances, based &#x043E;n the observed trends &#x0456;n the available data.</p>
<p>Specifically, we have identified several areas where the integrated approach appears promising, though further research &#x0456;s needed t&#x043E; confirm these findings. These areas include improvements &#x0456;n stress management, attention and impulse control, as well as overall psychological well-being. Additionally, we discussed how treatment personalization based &#x043E;n specific EEG profiles may represent a significant methodological innovation, enhancing treatment efficacy.</p>
<p>We recognize the importance &#x043E;f conducting future studies with greater methodological rigor, including active control groups and random assignment &#x043E;f subjects, t&#x043E; reduce the risk &#x043E;f bias and confirm the effectiveness &#x043E;f the intervention. Furthermore, we emphasize the need for clear and detailed reporting &#x043E;f statistical analyses and related data, with a particular focus &#x043E;n effect size measures, t&#x043E; provide a more robust understanding &#x043E;f the relationship between combined BF&#x2009;+&#x2009;NF training and the observed outcomes.</p>
<p>The small number of studies collected, together with the lack of statistical data (effect size measures), does not allow us to draw reliable conclusions to support the effectiveness and validity of an integrated BF&#x2009;+&#x2009;NF intervention. Therefore, as mentioned previously, ours represents a description of the literature present to date on the topic, with the aim of highlighting the potential results of using an integrated BF&#x2009;+&#x2009;NF approach and providing a narrative basis for any future studies. Further investigations are in fact necessary to determine the real usefulness of this method. These studies should be characterized by a more rigorous methodology, including an active control group (sham BF&#x2009;+&#x2009;NF) and the randomized assignment of subjects to each group, to reduce the risk of bias and be able to correlate any benefits observed with the treatment being studied of the study, thus limiting the probability of interference by confounding variables. Furthermore, as widely demonstrated by several studies (e.g., <xref ref-type="bibr" rid="ref69">Escolano et al., 2014</xref>; <xref ref-type="bibr" rid="ref15">Bazanova et al., 2018</xref>), it would be preferable to use individualized NF protocols, based on quantitative EEG (qEEG) measurements, which take into account consideration of individual variability in EEG profiles (<xref ref-type="bibr" rid="ref134">K&#x00F6;pruner et al., 1984</xref>; <xref ref-type="bibr" rid="ref131">Klimesch, 1999</xref>; <xref ref-type="bibr" rid="ref39">Clark et al., 2004</xref>) and allow the use of personalized protocols for each subject, thus maximizing the probability of treatment success. Furthermore, future research should report clearly and in great detail the type of statistical analysis carried out and the related data obtained, making particular reference to the effect size measures, thanks to which it would be possible to determine the strength of the relationship between the combined BF&#x2009;+&#x2009;NF training and the reduction of the symptoms of a specific pathology or the improvement of sporting or cognitive performance. Finally, follow-ups at multiple time intervals should be foreseen in the experimental procedure, in order to determine whether the results of the combined approach are maintained over time and to quantify their duration.</p>
<p>One final consideration concerns the distinction between the theoretical potential &#x043E;f integrated biofeedback (BF) and neurofeedback (NF) protocols and their practical application &#x0456;n clinical settings outside &#x043E;f academia. In practice, the availability and ease &#x043E;f use &#x043E;f combined protocols are largely dependent &#x043E;n the software and systems provided by vendors. This gap between the theoretical benefits &#x043E;f integrated BF and NF training and the practical challenges faced by practitioners underscores a critical need. Vendors play a crucial role &#x0456;n bridging this gap by developing more user-friendly, integrated solutions. Without vendor support &#x0456;n making these protocols more accessible and easier t&#x043E; implement, the potential for these innovative treatments to reach patients outside &#x043E;f academic research remains limited.</p>
<p>In conclusion, while acknowledging the significant contributions &#x043E;f previous studies, this review has unearthed new insights that enrich our understanding &#x043E;f the integrated use &#x043E;f biofeedback and neurofeedback techniques. Specifically, we have identified and highlighted:</p>
<list list-type="bullet">
<list-item>
<p>New areas &#x043E;f application: Our analysis has revealed that, despite the presence &#x043E;f prior studies, there are specific areas and conditions where the integrated BF&#x2009;+&#x2009;NF approach can be further explored t&#x043E; maximize therapeutic benefits and performance enhancement.</p>
</list-item>
<list-item>
<p>Methodological innovations: We have emphasized the importance &#x043E;f innovative methodological approaches &#x0456;n the application &#x043E;f BF and NF techniques, which can offer new perspectives &#x043E;n their therapeutic potential and mechanisms &#x043E;f action.</p>
</list-item>
<list-item>
<p>Practical implications for treatment personalization: Our review suggests that the integration &#x043E;f BF and NF could be personalized based &#x043E;n individual needs, offering potential for more targeted and effective treatments.</p>
</list-item>
</list>
<p>These insights contribute t&#x043E; a richer and more nuanced understanding &#x043E;f the integrated use &#x043E;f BF and NF, proposing new directions for future research and underscoring the need for further rigorous and methodologically innovative studies. We encourage researchers t&#x043E; build &#x043E;n these foundations, exploring uncharted potentials and refining treatment strategies t&#x043E; further improve clinical and performance outcomes.</p>
</sec>
<sec sec-type="author-contributions" id="sec14">
<title>Author contributions</title>
<p>BT: Conceptualization, Investigation, Writing &#x2013; original draft. SC: Conceptualization, Investigation, Writing &#x2013; original draft. SM: Methodology, Writing &#x2013; review &#x0026; editing. TDL: Methodology, Writing &#x2013; review &#x0026; editing. AR: Supervision, Writing &#x2013; review &#x0026; editing. AA: Supervision, Writing &#x2013; review &#x0026; editing. PD: Supervision, Writing &#x2013; review &#x0026; editing.</p>
</sec>
</body>
<back>
<sec sec-type="funding-information" id="sec15">
<title>Funding</title>
<p>The author(s) declare financial support was received for the research, authorship, and/or publication of this article. Project ECS 0000024 &#x201C;Ecosistema dell&#x2019;innovazione&#x2014;Rome Technopole&#x201D; financed by EU in NextGenerationEU plan through MUR Decree n. 1051 23.06.2022 PNRR Missione 4 Componente 2 Investimento 1.5&#x2014;CUP H33C22000420001.</p>
</sec>
<sec sec-type="COI-statement" id="sec16">
<title>Conflict of interest</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
<sec id="sec100" sec-type="disclaimer">
<title>Publisher&#x2019;s note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
</sec>
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