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<journal-id journal-id-type="publisher-id">Front. Virtual Real.</journal-id>
<journal-title>Frontiers in Virtual Reality</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Virtual Real.</abbrev-journal-title>
<issn pub-type="epub">2673-4192</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
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<article-id pub-id-type="publisher-id">1468971</article-id>
<article-id pub-id-type="doi">10.3389/frvir.2025.1468971</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Virtual Reality</subject>
<subj-group>
<subject>Original Research</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>To pre-process or not to pre-process? On the role of EEG enhancement for cybersickness characterization and the importance of amplitude modulation features</article-title>
<alt-title alt-title-type="left-running-head">Rosanne et al.</alt-title>
<alt-title alt-title-type="right-running-head">
<ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/frvir.2025.1468971">10.3389/frvir.2025.1468971</ext-link>
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<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Rosanne</surname>
<given-names>Olivier</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
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<sup>&#x2020;</sup>
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<contrib contrib-type="author">
<name>
<surname>Benesch</surname>
<given-names>Danielle</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
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<xref ref-type="fn" rid="fn1">
<sup>&#x2020;</sup>
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<name>
<surname>Kratzig</surname>
<given-names>Gregory</given-names>
</name>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
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<xref ref-type="fn" rid="fn1">
<sup>&#x2020;</sup>
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<contrib contrib-type="author">
<name>
<surname>Par&#xe9;</surname>
<given-names>Simon</given-names>
</name>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
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<sup>&#x2020;</sup>
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<contrib contrib-type="author">
<name>
<surname>Bolt</surname>
<given-names>Nicole</given-names>
</name>
<xref ref-type="aff" rid="aff5">
<sup>5</sup>
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<xref ref-type="fn" rid="fn1">
<sup>&#x2020;</sup>
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<contrib contrib-type="author" corresp="yes">
<name>
<surname>Falk</surname>
<given-names>Tiago H.</given-names>
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<xref ref-type="aff" rid="aff1">
<sup>1</sup>
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<xref ref-type="corresp" rid="c001">&#x2a;</xref>
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<sup>&#x2020;</sup>
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<aff id="aff1">
<sup>1</sup>
<institution>Institut National de la Recherche Scientifique</institution>, <institution>University of Qu&#xe9;bec</institution>, <addr-line>Montreal</addr-line>, <addr-line>QC</addr-line>, <country>Canada</country>
</aff>
<aff id="aff2">
<sup>2</sup>
<institution>Thales Research and Technology Canada</institution>, <addr-line>Qu&#xe9;bec City</addr-line>, <addr-line>QC</addr-line>, <country>Canada</country>
</aff>
<aff id="aff3">
<sup>3</sup>
<institution>Department of Psychology, University of Regina</institution>, <addr-line>Regina</addr-line>, <addr-line>SK</addr-line>, <country>Canada</country>
</aff>
<aff id="aff4">
<sup>4</sup>
<institution>Public Safety Canada</institution>, <addr-line>Ottawa</addr-line>, <addr-line>ON</addr-line>, <country>Canada</country>
</aff>
<aff id="aff5">
<sup>5</sup>
<institution>Department of Psychology and Health Studies, University of Saskatchewan</institution>, <addr-line>Saskatoon</addr-line>, <addr-line>SK</addr-line>, <country>Canada</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>
<bold>Edited by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/140329/overview">J. Adam Jones</ext-link>, Mississippi State University, United States</p>
</fn>
<fn fn-type="edited-by">
<p>
<bold>Reviewed by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/1132291/overview">Diego Vilela Monteiro</ext-link>, ESIEA University, France</p>
<p>
<ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/79980/overview">Thomas A. Stoffregen</ext-link>, University of Minnesota Twin Cities, United States</p>
</fn>
<corresp id="c001">&#x2a;Correspondence: Tiago H. Falk, <email>tiago.falk@inrs.ca</email>
</corresp>
<fn fn-type="other" id="fn1">
<label>
<sup>&#x2020;</sup>
</label>
<p>ORCID: Olivier Rosanne, <ext-link ext-link-type="uri" xlink:href="http://orcid.org/0009-0002-4445-3469">orcid.org/0009-0002-4445-3469</ext-link>; Danielle Benesch, <ext-link ext-link-type="uri" xlink:href="http://orcid.org/0000-0002-2002-2325">orcid.org/0000-0002-2002-2325</ext-link>; Gregory Kratzig, <ext-link ext-link-type="uri" xlink:href="http://orcid.org/0000-0003-1604-3729">orcid.org/0000-0003-1604-3729</ext-link>; Simon Par&#xe9;, <ext-link ext-link-type="uri" xlink:href="http://orcid.org/0009-0009-0759-5899">orcid.org/0009-0009-0759-5899</ext-link>; Nicole Bolt, <ext-link ext-link-type="uri" xlink:href="http://orcid.org/0000-0002-2498-0555">orcid.org/0000-0002-2498-0555</ext-link>; Tiago H. Falk, <ext-link ext-link-type="uri" xlink:href="http://orcid.org/0000-0002-5739-2514">orcid.org/0000-0002-5739-2514</ext-link>
</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>30</day>
<month>01</month>
<year>2025</year>
</pub-date>
<pub-date pub-type="collection">
<year>2025</year>
</pub-date>
<volume>6</volume>
<elocation-id>1468971</elocation-id>
<history>
<date date-type="received">
<day>22</day>
<month>07</month>
<year>2024</year>
</date>
<date date-type="accepted">
<day>07</day>
<month>01</month>
<year>2025</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#xa9; 2025 Rosanne, Benesch, Kratzig, Par&#xe9;, Bolt and Falk.</copyright-statement>
<copyright-year>2025</copyright-year>
<copyright-holder>Rosanne, Benesch, Kratzig, Par&#xe9;, Bolt and Falk</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>Virtual Reality (VR) has expanded beyond the entertainment field and has become a valuable tool across different verticals, including healthcare, education, and professional training, just to name a few. Despite these advancements, widespread usage of VR systems is still limited, mostly due to motion sickness symptoms, such as dizziness, nausea, and headaches, which are collectively termed &#x201c;cybersickness&#x201d;. In this paper, we explore the use of electroencephalography (EEG) as a tool for real-time characterization of cybersickness. In particular, we aim to answer three research questions: (1) what neural patterns are indicative of cybersickness levels, (2) do EEG amplitude modulation features convey more important and explainable patterns, and (3) what role does EEG pre-processing play in overall cybersickness characterization. Experimental results show that minimal pre-processing retains artifacts that may be useful for cybersickness detection (e.g., head and eye movements), while more advanced methods enable the extraction of more interpretable neural patterns that may help the research community gain additional insights on the neural underpinnings of cybersickness. Our experiments show that the proposed amplitude modulation features comprise roughly 60% of the top-selected features for EEG-based cybersickness detection.</p>
</abstract>
<kwd-group>
<kwd>cybersickness</kwd>
<kwd>virtual reality</kwd>
<kwd>electroencephalography</kwd>
<kwd>amplitude modulation</kwd>
<kwd>artifact removal</kwd>
</kwd-group>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-at-acceptance</meta-name>
<meta-value>Virtual Reality and Human Behaviour</meta-value>
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</front>
<body>
<sec id="s1">
<title>1 Introduction</title>
<p>Virtual Reality (VR) has experienced significant growth in recent years due to advances in hardware technology and its increasing availability to the general public. Today, it is a widely adopted solution in various fields beyond entertainment, including medicine, therapy, and professional training, just to name a few (<xref ref-type="bibr" rid="B12">Angelov et al., 2020</xref>; <xref ref-type="bibr" rid="B136">Stecu&#x142;a, 2022</xref>; <xref ref-type="bibr" rid="B31">Cassani et al., 2020a</xref>). One of the reasons for its success is its ability to create highly realistic and modular environments at fairly low costs. This can provide exposure therapy for patients with, e.g., obsessive-compulsive disorder and post-traumatic stress disorder (<xref ref-type="bibr" rid="B39">Cullen et al., 2021</xref>; <xref ref-type="bibr" rid="B96">Maples-Keller et al., 2017</xref>) or allow for cost-effective training in various sectors, such as aerospace or remote surgery (e.g. (<xref ref-type="bibr" rid="B121">Rojas-S&#xe1;nchez et al., 2023</xref>; <xref ref-type="bibr" rid="B18">Barteit et al., 2021</xref>; <xref ref-type="bibr" rid="B46">Dymora et al., 2021</xref>; <xref ref-type="bibr" rid="B49">Fracaro et al., 2021</xref>)). Moreover, for training of law enforcement officers, VR is crucial to allow them to practice decision-making, communication, and tactical skills in computer-generated scenarios that closely resemble real-world situations. This overcomes logistical constraints and allows for training of cadets in safety-critical situations that would not otherwise be possible in the real-world (<xref ref-type="bibr" rid="B84">Koutitas et al., 2021</xref>; <xref ref-type="bibr" rid="B104">Mu&#xf1;oz et al., 2020</xref>; <xref ref-type="bibr" rid="B99">Mills et al., 2020</xref>).</p>
<p>However, the widespread adoption of VR has been hindered by a factor termed &#x2018;cybersickness&#x2019;, which is akin to motion sickness experienced by many in boats and moving cars. Cybersickness is characterized by symptoms such as dizziness, nausea, headaches, disorientation, vertigo, visual disturbances, and increased salivation. It can vary significantly among individuals and can be influenced by numerous factors, including age, gender (<xref ref-type="bibr" rid="B52">Gamito et al., 2008</xref>), prior VR exposure, characteristics of the VR system and the displayed content (e.g., resolution, field of view, motion dynamics, frame rate), as well as behavioural factors such head movements or standing versus sitting (<xref ref-type="bibr" rid="B101">Moss and Muth, 2011</xref>). The root causes of cybersickness and its variability across the general population are still unknown. The sensory conflict theory posits that cybersickness primarily arises from discrepancies between visual inputs and vestibular sensory feedback (<xref ref-type="bibr" rid="B32">Celikcan, 2019</xref>). Many studies have been interpreted in relation to the sensory conflict theory to explain the relationship between VR system specifications, content design, and cybersickness symptoms (<xref ref-type="bibr" rid="B128">Sawada et al., 2020</xref>; <xref ref-type="bibr" rid="B77">Kim et al., 2020</xref>; <xref ref-type="bibr" rid="B61">Irmak et al., 2023</xref>). However, these findings are often compatible with other etiological theories, and the results are not exclusive to sensory conflict explanations (<xref ref-type="bibr" rid="B135">Stanney et al., 2020</xref>). While the sensory conflict theory provides a framework for understanding cybersickness, it did not directly influence the design of this study, which instead focused on identifying neural markers associated with symptom intensity.</p>
<p>The traditional method of assessing cybersickness involves subjective questionnaires, such as the Simulator Sickness Questionnaire (SSQ) and the Fast Motion Sickness (FMS) (<xref ref-type="bibr" rid="B75">Keshavarz and Hecht, 2011</xref>). Notwithstanding, while subjective tests are valuable for quantifying the multidimensional impact of cybersickness, disrupting users to continuously report on their symptoms can negatively impact the immersiveness of the application. In recent years, there has been a push for more objective measures based on processing of different biosignals and user behaviours. These methods offer a more objective measure of the user&#x2019;s physiological state, enhancing our understanding and ability to quantify and compare the effectiveness of different VR systems and content designs to mitigate cybersickness.</p>
<p>VR hardware today is equipped with numerous sensors that may be useful to characterize cybersickness. For example, several commercial head-mounted displays (HMDs) are equipped with IMUs (inertial measurement units) that can help track head movements, eye trackers to monitor gaze changes, and photoplethysmography (PPG) sensors to measure heart rate and heart rate variability. These sensors could be useful in monitoring discrepancies in perceived motion and orientation in space (<xref ref-type="bibr" rid="B94">Lopes et al., 2020</xref>), as well as in physiological changes such as heart rate (<xref ref-type="bibr" rid="B79">Kim et al., 2022</xref>), postural instability (<xref ref-type="bibr" rid="B119">Risi and Palmisano, 2019</xref>), and visual fatigue (<xref ref-type="bibr" rid="B134">Souchet et al., 2023</xref>), among others. These measures have been shown useful in predicting cybersickness severity (<xref ref-type="bibr" rid="B15">Arcioni et al., 2019</xref>; <xref ref-type="bibr" rid="B62">Islam et al., 2021</xref>; <xref ref-type="bibr" rid="B131">Shimada et al., 2023a</xref>; <xref ref-type="bibr" rid="B116">Reyero Lobo and Perez, 2022</xref>; <xref ref-type="bibr" rid="B76">Kim, 2024</xref>; <xref ref-type="bibr" rid="B130">Setiowati et al., 2020</xref>; <xref ref-type="bibr" rid="B149">Wang et al., 2022</xref>).</p>
<p>Moreover, there is a recent trend to add additional (bio)sensors to VR headsets. For example, the Galea and Kaptics headsets have proposed the inclusion of sensors such galvanic skin response (GSR), skin temperature, and electroencephalography (EEG) (<xref ref-type="bibr" rid="B21">Bernal et al., 2022</xref>; <xref ref-type="bibr" rid="B30">Cassani et al., 2020b</xref>). GSR can be useful in detecting sweat, a cybersickness symptom (<xref ref-type="bibr" rid="B42">Dennison et al., 2016</xref>; <xref ref-type="bibr" rid="B64">Islam et al., 2020</xref>; <xref ref-type="bibr" rid="B55">Guna et al., 2020</xref>), but also changes in mental states such as stress (<xref ref-type="bibr" rid="B53">Garrido et al., 2022</xref>) and cognitive load (<xref ref-type="bibr" rid="B129">Sepich et al., 2022</xref>), which could be due to cybersickness or other external factors (<xref ref-type="bibr" rid="B74">Katsigiannis et al., 2018</xref>; <xref ref-type="bibr" rid="B150">Wu and Lin, 2011</xref>). EEG, in turn, provides a real-time glimpse of neural changes linked to cybersickness (<xref ref-type="bibr" rid="B85">Krokos and Varshney, 2022</xref>; <xref ref-type="bibr" rid="B151">Yang et al., 2022a</xref>), potentially guiding new interventions to mitigate symptoms [e.g. (<xref ref-type="bibr" rid="B19">Benelli et al., 2023</xref>)]. Very recently, several works have suggested that to more accurately predict cybersickness, multiple signal modalities need to be explored concurrently, in particular EEG, electrocardiography (ECG), eye movements, and head movements (<xref ref-type="bibr" rid="B63">Islam et al., 2022</xref>; <xref ref-type="bibr" rid="B69">Jeong et al., 2023</xref>; <xref ref-type="bibr" rid="B114">Qu et al., 2022</xref>; <xref ref-type="bibr" rid="B60">Hwang et al., 2022</xref>; <xref ref-type="bibr" rid="B100">Moinnereau and Falk, 2024</xref>). Electrogastrography (EGG) has also shown to be useful in characterizing cybersickness, but requires electrodes to be placed around the participant&#x2019;s abdomen area, which could disrupt the user&#x2019;s immersive experience (<xref ref-type="bibr" rid="B137">Stern, 2002</xref>; <xref ref-type="bibr" rid="B154">Yin and Chen, 2013</xref>; <xref ref-type="bibr" rid="B65">Jakus et al., 2022</xref>).</p>
<p>Characterizing cybersickness using biosignals has some disadvantages. For example, signals are often contaminated with artifacts. While automated pre-processing algorithms exist [e.g. (<xref ref-type="bibr" rid="B153">Yildirim, 2020</xref>; <xref ref-type="bibr" rid="B40">Delorme, 2023</xref>)], it is not clear what impact they may have on signal patterns and, ultimately, on downstream cybersickness characterization tasks. As an example, automated pre-processing of EEG signals has shown to affect different diagnostic tasks, such as Alzheimer&#x2019;s disease diagnosis (<xref ref-type="bibr" rid="B29">Cassani et al., 2014</xref>). Moreover, when it comes to electrical biosignals, physiological processes often serve as contaminants. With EEG, for example, signals may be contaminated by heart beats, as well as by eye and/or head movements. In this case, removal of eye/head movement artifacts may indeed be removing information that could help characterize cybersickness.</p>
<p>Lastly, the latest trend in biosignal processing has involved the use of deep learning for both feature extraction and classification (<xref ref-type="bibr" rid="B153">Yildirim, 2020</xref>; <xref ref-type="bibr" rid="B90">Liao et al., 2020</xref>; <xref ref-type="bibr" rid="B92">Liu et al., 2024</xref>). In these scenarios, there is little interpretability and explainability (<xref ref-type="bibr" rid="B70">Jeong et al., 2019</xref>; <xref ref-type="bibr" rid="B47">Fan et al., 2021</xref>). As such, while prediction/detection of cybersickness is possible with high accuracy, few insights on what occurs in the brain/body during cybersickness are available, thus limiting the development of tactics to reduce symptoms. Moreover, existing datasets are relatively small and with a small number of subjects, which can likely lead to overfitting by highly-complex models (<xref ref-type="bibr" rid="B153">Yildirim, 2020</xref>; <xref ref-type="bibr" rid="B147">Tsimenidis, 2020</xref>), as well as to limited generalization capability (<xref ref-type="bibr" rid="B124">Roy et al., 2019</xref>).</p>
<p>In this paper, we aim to take a different approach to cybersickness detection. First, we explore the impact of different levels of artifact removal&#x2013;from very basic techniques where head/body artifacts are kept, to more advanced pipelines leaving only neural signatures for evaluation&#x2013;on cybersickness characterization. While the former effectively transforms the EEG into an embedded multimodal system, thus potentially improving detection accuracy, the latter can uncover the specific neurological patterns associated with cybersickness, thus leading to potential interventions to mitigate symptoms. Second, we extend our analysis beyond EEG conventional Power Spectral Density (PSD) features and propose the use of EEG Amplitude Modulation (AM) and connectivity features for detection of cybersickness symptoms, offering a complementary perspective on the neural interactions underlying cybersickness symptoms. AM analysis has shown to be useful for mental and cognitive state characterization (<xref ref-type="bibr" rid="B10">Albuquerque et al., 2020</xref>; <xref ref-type="bibr" rid="B37">Clerico et al., 2015</xref>; <xref ref-type="bibr" rid="B38">Clerico et al., 2018</xref>), as well as for health diagnostics (<xref ref-type="bibr" rid="B50">Fraga et al., 2013</xref>; <xref ref-type="bibr" rid="B146">Trambaiolli et al., 2011</xref>). To the best of our knowledge, this is the first time that AM features are being explored for cybersickness measurement.</p>
<p>AM is a second-order spectral analysis which aims to capture the temporal variations of amplitudes in cortical oscillations. It consists in constructing a frequency representation from the envelope of these oscillations. This hidden structure in EEG signals reflects the interaction between several fundamental mechanisms that occur naturally in the brain (<xref ref-type="bibr" rid="B24">Bondar&#x2019; and Fedotchev, 2000</xref>; <xref ref-type="bibr" rid="B57">Hidalgo et al., 2022</xref>; <xref ref-type="bibr" rid="B58">Hilla et al., 2020</xref>), and therefore may provide greater insights for cybersickness characterization.</p>
<p>Three different ablation studies are conducted to investigate the impact of the Automatic Artifact Removal (AAR) algorithm used, epoch size, and number of features. These ablation studies are used to find the optimal combination of such factors, which are then used to find the best cybersickness prediction model to be tested on an unseen test set. The goal of the first ablation study is to evaluate the efficacy of each AAR algorithm at removing head and eye movements. In the second ablation study, we investigate the predictive power of different combinations of AAR algorithms, feature types, and epoch sizes. Lastly, in the third ablation study, we explore the optimal number of features for cybersickness prediction.</p>
<p>The remainder of this paper is as follows: <xref ref-type="sec" rid="s2">Section 2</xref> will describe the methods and materials used in the study, while <xref ref-type="sec" rid="s3">Section 3</xref> presents the obtained results. <xref ref-type="sec" rid="s4">Section 4</xref> will discuss the implications of our findings and, finally, <xref ref-type="sec" rid="s5">Section 5</xref> will conclude the paper and suggest directions for future research.</p>
</sec>
<sec sec-type="materials|methods" id="s2">
<title>2 Materials and methods</title>
<sec id="s2-1">
<title>2.1 Dataset</title>
<p>For this study, we relied on a cybersickness dataset described in <xref ref-type="bibr" rid="B86">Li et al. (2021)</xref>, which followed an experimental protocol specifically designed to induce cybersickness. Data was collected from 20 participants who were immersed in two VR scenarios: a tunnel travel simulation and a roller coaster ride. The &#x2018;Tunnel&#x2019; session emphasized strong linear vection with minimal rotational motion to induce mild to moderate cybersickness. Participants who did not reach a cybersickness threshold of 11/20 on the Fast Motion Sickness (FMS) scale after 10 repetitions (approximately 10&#xa0;min) proceeded to the &#x2018;Roller Coaster&#x2019; session. This session included similar linear vection but added stronger rotational motion to intensify symptoms, ensuring that all participants reached sufficient cybersickness levels to enable subsequent analyses. The rationale behind these tasks was to account for individual differences in susceptibility while ensuring sensory conflict through visual motion without movements.</p>
<p>Each session lasted up to 10&#xa0;min, with the duration tailored to individual participant responses, as indicated by their cybersickness levels. Cybersickness severity was systematically measured using the 20-point FMS questionnaire, administered at the end of each minute, for as long as the participants could manage their symptoms until reaching an FMS score of 11. Some participants did not experience cybersickness and reported FMS values not exceeding 4 (out of 20). Specifically, subjects 1, 3, 10 and 15 in the Tunnel session and subjects 1, 3, 10 and 16 in the Roller coaster session. In addition, data from 10 subjects in the Roller Coaster session was not available since these subjects did not continue to the second part of the experiment due to severe discomfort after the first video. In the roller coaster session only the data from subjects 7, 8, 11, 13, 15 and 20 were included in the analysis.</p>
<p>The study recorded multi-channel EEG, 1-channel Electrooculography (EOG), and head movements via a 3-axis accelerometer. The seven EEG channel locations used in this study included Fz, Pz, P3, P4, Cz, CP5, and CP6, recording with a sampling rate of 500&#xa0;Hz. The EOG channel, located on the left lower eyelid, was used to monitor eye movements and eye blinks. Both the ground and reference electrodes were connected together and attached to the right earlobe using an ear clip. The interested reader is referred to <xref ref-type="bibr" rid="B86">Li et al. (2021)</xref> for complete details about the data collection process and the dataset used.</p>
</sec>
<sec id="s2-2">
<title>2.2 Pre-processing</title>
<p>Pre-processing is crucial in EEG research to remove unwanted physiological (e.g., heart beats, muscle/eye/head movements) and environmental (e.g., powerline, temperature, humidity) interferences (<xref ref-type="bibr" rid="B141">Tanner et al., 2016</xref>; <xref ref-type="bibr" rid="B23">Bigdely-Shamlo et al., 2020</xref>). With such pre-processing algorithms, a trade-off must always be achieved between the aggressiveness of the artifact removal step and the potential (unwanted) removal of useful discriminatory information from the collected signals (<xref ref-type="bibr" rid="B40">Delorme, 2023</xref>; <xref ref-type="bibr" rid="B120">Robbins et al., 2020</xref>). For example, AAR algorithms based on Independent Component Analysis (ICA) are susceptible to causing phase distortion (<xref ref-type="bibr" rid="B142">Thatcher et al., 2020</xref>) and/or loss of useful information (<xref ref-type="bibr" rid="B126">Sadiya et al., 2021</xref>; <xref ref-type="bibr" rid="B81">Klug and Gramann, 2021</xref>). Similarly, rejecting channels and segments of the signal contaminated by artifacts introduces information loss and discontinuities (<xref ref-type="bibr" rid="B126">Sadiya et al., 2021</xref>; <xref ref-type="bibr" rid="B59">Huberty et al., 2024</xref>).</p>
<p>With cybersickness prediction, however, artifact removal may play a crucial role, as the information that is often removed, such as head movements, eye movements, and heart beats, may indeed help in the prediction process. As such, here we explore three different levels of AAR, from light to aggressive, to gauge the effect this has on cybersickness characterization, as well as on the insights generated by the top features later used for the prediction task. This, in fact, has been recently emphasized in <xref ref-type="bibr" rid="B40">Delorme (2023)</xref> where a reduction in the amount of pre-processing was suggested to prevent the loss of relevant neural information of event related potentials. In addition, authors in <xref ref-type="bibr" rid="B142">Thatcher et al. (2020)</xref> demonstrate that AAR based on ICA result in phase distortion that could compromise connectivity analysis. The three different pre-processing techniques explored herein are detailed next.</p>
<sec id="s2-2-1">
<title>2.2.1 Minimal pre-processing</title>
<p>Inspired by the work in <xref ref-type="bibr" rid="B40">Delorme (2023)</xref>, an extremely simple pre-processing pipeline&#x2013;called &#x2018;Minimal&#x2019; &#x2013; was tested to minimize potential distortion of the EEG signals at the cost of limited noise reduction. The &#x2018;Minimal&#x2019; pre-processing strategy comprised exclusively of a high-pass filtering using a zero-phase Butterworth filter set to a cutoff frequency of 0.25&#xa0;Hz used to eliminate low-frequency drift. This method should preserve artifacts related to eye, muscle, and head movements, as well as powerline interference. Previous studies [e.g. (<xref ref-type="bibr" rid="B157">Zao et al., 2016</xref>; <xref ref-type="bibr" rid="B35">Chang et al., 2021</xref>; <xref ref-type="bibr" rid="B72">Jin et al., 2018</xref>)] have demonstrated the utility of EOG and head movement data in cybersickness detection, motivating our exploration of whether these signals could be indirectly captured and utilized from EEG alone.</p>
</sec>
<sec id="s2-2-2">
<title>2.2.2 Artifact subspace reconstruction pre-processing</title>
<p>In this second approach, the widely-used artifact Subspace Reconstruction (ASR) algorithm (<xref ref-type="bibr" rid="B102">Mullen et al., 2013</xref>) followed by an independent component rejection step using the ICLabel algorithm (<xref ref-type="bibr" rid="B112">Pion-Tonachini et al., 2019</xref>) was used. This configuration is known to remove many common EEG artifacts and to minimally interfere with relevant EEG information (<xref ref-type="bibr" rid="B40">Delorme, 2023</xref>). It is important to note that, while the efficiency of ICA may be reduced when applied to datasets with a small number of channels, empirical evidence suggests that ICA-based pre-processing has performed satisfactorily despite these limitations (<xref ref-type="bibr" rid="B115">Rejer and G&#xf3;rski, 2015</xref>). Following ASR pre-processing, any removed channels were replaced using default EEGLAB spherical interpolation (<xref ref-type="bibr" rid="B41">Delorme and Makeig, 2004</xref>), ensuring a consistent dataset for subsequent analyses.</p>
</sec>
<sec id="s2-2-3">
<title>2.2.3 Data-driven pre-processing</title>
<p>Automatic artifact detection algorithms, such as ASR, utilize threshold-based techniques or depend upon predefined templates and assumptions about the nature of EEG noise. In contrast to these conventional approaches, data-driven pre-processing pipelines make use of experiment-specific artifact data from both EOG and head movement measurements thereby offering more precise noise reduction of specific types of distortion.</p>
<p>Regression ICA (RegICA) is one such method which combines blind source separation and regression to more accurately remove, e.g., ocular artifacts (<xref ref-type="bibr" rid="B80">Klados et al., 2011</xref>). Here, RegICA is used to dynamically attenuate EEG frequency components that originate from non-neuronal sources, such as ocular and head movements. Reference signals (i.e., EOG and head accelerometry) are used to characterize components of the EEG signal that have high correlations (here, characterized as a correlation greater than 0.25) with the non-neuronal signal.</p>
<p>Since EEG signals and reference signals have very different magnitudes, the data was scaled by subtracting the median of each channel and dividing by the median absolute deviation to avoid numerical instability. Subsequently, RegICA is applied twice: initially using the head accelerometer signals as references, and then using EOG signals. Here, the following hyperparameters are used: a filter order of 3, sigma of 0.01, a forgetting factor of 0.999 and stable root mean square error as the optimization criterion. Using both EOG and accelerometer signals as reference with RegICA should remove eye and head movements in a data-driven manner.</p>
</sec>
</sec>
<sec id="s2-3">
<title>2.3 Feature extraction</title>
<sec id="s2-3-1">
<title>2.3.1 Power spectral density and coupling</title>
<p>Traditional methods have relied on conventional power spectral density measures computed for different EEG frequency bands, namely,: delta (1&#x2013;4&#xa0;Hz), theta (4&#x2013;8&#xa0;Hz), alpha (8&#x2013;12&#xa0;Hz), beta (12&#x2013;30&#xa0;Hz), and gamma (30&#x2013;50&#xa0;Hz) bands (<xref ref-type="bibr" rid="B87">Li et al., 2022</xref>; <xref ref-type="bibr" rid="B109">Ozkan et al., 2023</xref>). Here, band decomposition was achieved using a filter bank (FB) of zero-phase Finite impulse response (FIR) filter, which applied two successive filtering steps in opposite directions on a mirror-padded version of the input signal, thereby producing Band-filtered time series (BFT). Band-filtered time series were then epoched with window sizes corresponding to 2, 5, 8, 20 and 30&#xa0;s and shifts of 2&#xa0;s.</p>
<p>Power values were computed per sub-band by squaring the samples and then normalizing by the total EEG power. Three statistical functionals are then used to aggregate the per-epoch features: mean, standard deviation, and skewness. This approach resulted in 105 PSD candidate features per epoch duration (5 bands <inline-formula id="inf1">
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<p>Moreover, to measure the coupling between brain regions (i.e., between different electrodes) and between EEG frequency bands, a coupling measure is computed using either the Pearson correlation or mutual information to measure linear and non-linear properties, respectively, between different electrode pairs or frequency bands (<xref ref-type="bibr" rid="B38">Clerico et al., 2018</xref>; <xref ref-type="bibr" rid="B6">Akhand et al., 2024</xref>; <xref ref-type="bibr" rid="B3">Afshani et al., 2019</xref>; <xref ref-type="bibr" rid="B95">Lu et al., 2011</xref>). Here, Inter-channel coupling (CCPL) accounts for 630 candidate features (2 coupling types <inline-formula id="inf6">
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</sec>
<sec id="s2-3-2">
<title>2.3.2 Amplitude modulation features and coupling</title>
<p>To derive the AM time series, we first extract the temporal envelope of each of the five BFT employed for the extraction of PSD features. This initial step is represented in the top left block of <xref ref-type="fig" rid="F1">Figure 1A</xref>, which shows how the raw signal is filtered by the filter bank. The &#x2018;envelope extraction&#x2019; block consists of computing the analytical representation of the signal by applying a Hilbert transform. In this process, the Hilbert transform is implemented using a Kaiser-windowed sinc FIR filter. The envelope is then extracted from the norm of the analytical representation. Finally, we further decompose the envelopes using the same five bands, represented in <xref ref-type="fig" rid="F1">Figure 1A</xref> by five BFT blocks, resulting in a total of 25 AM time series. The matrix at the bottom of <xref ref-type="fig" rid="F1">Figure 1A</xref> depicts the AM time series resulting from this process.</p>
<fig id="F1" position="float">
<label>FIGURE 1</label>
<caption>
<p>
<bold>(A)</bold> Data flow diagram presenting each step of the AM time series extraction process. Blue arrows and cells correspond to meaningful AM band while bands marked as red are discarded. <bold>(B)</bold> Abstract data flow showing the general extraction process of coupling measurements from a set of time series. The combination operation generates all unique pairs of channels or bands. Unique pairs refer to the unique occurrence of joint elements regardless of their order. For example, both pairs (P3, P4) and (P4, P3) refer to the same coupling measure, therefore to prevent redundancy in the coupling analysis only one occurrence is kept. <bold>(C)</bold> Schematic representing how time series are selected for the computation of either AM-CCPL or AM-BCPL.</p>
</caption>
<graphic xlink:href="frvir-06-1468971-g001.tif"/>
</fig>
<p>However, according to Bedrosian&#x2019;s theorem (<xref ref-type="bibr" rid="B144">Trajin et al., 2008</xref>), only 14 of these 25 series are considered valid due to the inappropriate modulation of low-frequency bands by high-frequency bands resulting in signals that are not physically meaningful. The valid AM bands are represented in blue in <xref ref-type="fig" rid="F1">Figure 1A</xref>. The interested reader is referred to <xref ref-type="bibr" rid="B50">Fraga et al. (2013)</xref>; <xref ref-type="bibr" rid="B27">Cassani and Falk (2018)</xref> for a more comprehensive exploration of the features derived from AM.</p>
<p>For these new AM features, the epoch duration is a critical parameter, as it directly influences the latency in feature extraction and resolution. Furthermore, identifying the optimal epoch duration is essential for gaining insights into the temporal dynamics at which cybersickness-related neuronal patterns become discernible. In the literature, epoch durations when using AM features have ranged from 5, 8, to 20&#xa0;s (<xref ref-type="bibr" rid="B50">Fraga et al., 2013</xref>; <xref ref-type="bibr" rid="B28">Cassani and Falk, 2019</xref>; <xref ref-type="bibr" rid="B145">Trambaiolli et al., 2020</xref>) to effectively capture neuronal patterns needed for diagnostics.</p>
<p>As this is the first attempt at using these features for cybersickness detection, we leave epoch size as a hyper-parameter to be optimized in the experiments. To capture potential transient micro-state changes (<xref ref-type="bibr" rid="B105">Nam et al., 2022</xref>; <xref ref-type="bibr" rid="B34">Chang et al., 2023</xref>; <xref ref-type="bibr" rid="B16">Aubonnet et al., 2023</xref>), shorter windows are also explored. For completeness, we explore epoch sizes of 2, 5, 8, 20, and 30&#xa0;s. The power in each of the 14 <inline-formula id="inf16">
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<p>Moreover, as with spectral coupling measures, coupling between different AM times series was shown in <xref ref-type="bibr" rid="B38">Clerico et al. (2018)</xref> to better characterize different mental states. As such, AM-CCPL is used to capture interactions between every possible pair of channels, while AM-BCPL to measure coupling across all possible cross-band combinations. <xref ref-type="fig" rid="F1">Figures 1B, C</xref> depict the processing steps to compute the coupling parameters for the two different scenarios, respectively. <xref ref-type="fig" rid="F1">Figure 1C</xref> depicts the process of selecting channels or bands (indicated by green and blue colors, respectively) and combining them to compute AM-CCPL and AM-BCPL features. The green color represents selected channels that are paired to compute spatial interactions (AM-CCPL), while the blue color represents selected bands that are paired to compute spectral interactions (AM-BCPL). The pairing itself is handled by the process illustrated in <xref ref-type="fig" rid="F1">Figure 1B</xref>. In both cases, the notation used for AM-CCPL and AM-BCPL AM_{feature subtype}_{statistic} c &#x3d; <inline-formula id="inf21">
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</sec>
</sec>
<sec id="s2-4">
<title>2.4 Testing setup</title>
<p>
<xref ref-type="fig" rid="F2">Figure 2</xref> illustrates the general testing methodology employed in this experiment. With the dataset used, cybersickness FMS ratings were provided every minute.</p>
<fig id="F2" position="float">
<label>FIGURE 2</label>
<caption>
<p>Flowchart presenting the testing methodology which is divided into two main stages: Tuning stage (top light grey area) relies on the validation set (33% of the original dataset). Training and testing stage (bottom white area) relies on the development set (67% of the original dataset). <bold>(A)</bold> Features are ranked using their correlation with the FMS score. <bold>(B)</bold> Incremental cross-validation determines the optimal number of features, ensuring only the top features are retained in the development set. <bold>(C)</bold> The validation set is used to find the best hyperparameters for SVR. Once the tuning stage is completed, the optimal features and hyperparameters are used to train and validate the model <bold>(D)</bold>.</p>
</caption>
<graphic xlink:href="frvir-06-1468971-g002.tif"/>
</fig>
<p>FMS scores were recorded by participants at the end of each 1-min interval, while the EEG data used in regression analysis were taken from the same 1-min segment. This means that EEG trials could correspond to any moment within the interval-potentially near the beginning or end of the minute-relative to the reported FMS score. This approach may introduce a small temporal mismatch between the EEG features and the moment the FMS score reflects. As such, in this study we are measuring the cybersickness level (given by the FMS score) on a per-minute basis. Future studies could take this further and use the EEG trials to predict cybersickness levels many minutes ahead.</p>
<p>To augment the amount of data available for training of the classifiers, a bootstrapping method was applied where a random selection of epochs within a certain 1-min EEG segment under the same FMS rating were used. The statistical functionals, such as mean, standard deviation, and skewness were then computed from the resulting subset. This process can be repeated multiple times where after each iteration a distinct set is created. The number of epochs taken per 1-min segment and the number of times this bootstrap sampling was done was empirically set to 75% of total epoch number within the minute and 10 repetitions, respectively.</p>
<p>The data augmentation process produced a total of 712 samples from the collected data, as compared to the 7,035 features extracted for analysis. Feature selection methods were implemented to mitigate the high sample-to-feature ratio, ensuring a more robust and interpretable regression model. The tuning stage involved the use of a validation set to estimate the best subset of features, as depicted in <xref ref-type="fig" rid="F2">Figures 2A, B</xref>.</p>
<p>To avoid data leakage between training and test samples, a Stratified-group K-fold methodology was used to restrict groups of samples from the same minute segment to a unique data subset (i.e., train or test). This step corresponds to item (d) in <xref ref-type="fig" rid="F2">Figure 2</xref>. Train and test set were generated from the development set which correspond to a portion of 67% of samples reserved exclusively for training and testing. Hyperparameters of the support vector regression model were optimized using the validation set, as represented by <xref ref-type="fig" rid="F2">Figure 2C</xref>, during the tuning stage.</p>
</sec>
<sec id="s2-5">
<title>2.5 Post-processing</title>
<p>After extracting features from each EEG recording session, outlier detection was conducted independently on each feature using a threshold of three times the median absolute deviation. Detected outliers, along with near infinite, near zero, and missing samples (Not-A-Number), were corrected via linear interpolation of time contiguous samples. Lastly, FMS ratings were normalized to a scale ranging from 0 to 1 to facilitate the use of the root-mean-square error (RMSE) as a figure-of-merit to gauge system accuracy.</p>
</sec>
<sec id="s2-6">
<title>2.6 Feature ranking and selection</title>
<p>Given that the used dataset has a low sample-to-feature ratio, feature selection is needed to reduce the number of features to a manageable number to prevent overfitting. Additionally, to mitigate the risk of data leakage, features selection is performed on a validation subset (set as 33% samples of the dataset) of the data using the &#x201c;StratifiedGroupKFold&#x201d; module within scikit-learn (<xref ref-type="bibr" rid="B111">Pedregosa et al., 2011</xref>) prior to the train/test split procedure. This approach ensures that the validation samples come from different time instances than those reserved for testing, keeping the test set completely unseen.</p>
<p>Here, a simple feature ranking method was utilized based on Spearman correlation. For each feature, the correlation was calculated between samples and their corresponding FMS rating. This process is represented by step (a) in <xref ref-type="fig" rid="F2">Figure 2</xref>. The correlation score attributed to each feature is used in ablation study II presented in <xref ref-type="sec" rid="s3-2">Section 3.2</xref>.</p>
<p>The rank ordering was based firstly by statistical significance (Holm-Bonferroni corrected with significance set at a threshold of 0.05), followed by absolute Spearman correlation coefficient values. After this ranking, the top 100 features were selected (empirically) for further analysis. To gauge the impact of including additional features on cybersickness measurement, top-features were added one by one and regression performance on the validation set was assessed via stratified 5-fold cross-validation. This step corresponds to item (b) of the Tuning stage presented in <xref ref-type="fig" rid="F2">Figure 2</xref>; this step further described in the ablation study III in <xref ref-type="sec" rid="s3-3">Section 3.3</xref>. The final number of features to be used is the one that leads to the smallest RMSE value obtained on the validation set after Gaussian smoothing.</p>
</sec>
<sec id="s2-7">
<title>2.7 Regression analysis</title>
<p>A Support Vector Regressor (SVR) was selected as the regression algorithm, motivated by its robustness to overfitting, a characteristic particularly advantageous for high dimensional datasets. Hyper-parameter optimization for the SVR model was carried out through an exhaustive 3-fold cross-validation grid search, exploring combinations of 3 &#xd7; 4 &#xd7; 20x20 for kernel types (&#x2018;poly&#x2019;, &#x2018;rbf&#x2019;, and &#x2018;sigmoid&#x2019;), polynomial degrees (2 through 5), and the parameters C and gamma. The search covered logarithmic scales from <inline-formula id="inf25">
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</sec>
</sec>
<sec sec-type="results" id="s3">
<title>3 Results</title>
<p>The following sub-sections presents the results of a series of ablation studies aimed at examining the impact of different EEG pre-processing methods, feature types, and epoch sizes on cybersickness prediction. Ablation studies are analytical approaches used to investigate the contribution of specific components or processing steps to the performance of a predictive model. By systematically isolating and testing individual factors, such as pre-processing strategies or feature sets, these studies allow us to evaluate their independent effects on the inference process.</p>
<sec id="s3-1">
<title>3.1 Ablation study I: artifacts and artifact removal</title>
<p>To better understand the impact of head movements and eye movements on certain EEG frequency bands, <xref ref-type="fig" rid="F3">Figures 3</xref>, <xref ref-type="fig" rid="F4">4</xref> depict (top plots) the power spectral representation of the accelerometer signals (averaged across the x, y, and <italic>z</italic>-axes) and the Signal-to-Noise Ratio (SNR) representation (bottom plot), for each of these two signal modalities, respectively. SNR is computed for each frequency bin as the ratio between the power of the bin&#x2019;s central frequency and the mean power of neighboring frequencies excluding immediately adjacent ones (<xref ref-type="bibr" rid="B97">Meigen and Bach, 1999</xref>).</p>
<fig id="F3" position="float">
<label>FIGURE 3</label>
<caption>
<p>
<bold>(A)</bold> Spectral analysis of accelerometer data: This graph presents the spectral representation of accelerometer data averaged across the x, y, and <italic>z</italic>-axes for multiple subjects and sessions. On the <italic>y</italic>-axis, power is expressed in decibels (dB), while the <italic>x</italic>-axis displays frequency in Hertz (Hz), covering a spectrum from 1&#xa0;Hz to 50&#xa0;Hz. The blue curve illustrates the mean power spectrum, and the shaded area represents the standard deviation, reflecting variability across recordings. <bold>(B)</bold> Signal-to-Noise Ratio (SNR): This part of the figure presents the SNR across the frequency spectrum, amplifying local activity in relation to adjacent background noise levels. The <italic>x</italic>-axis displays the frequency in Hertz (Hz), covering the same range as in Figure <bold>(A)</bold>.</p>
</caption>
<graphic xlink:href="frvir-06-1468971-g003.tif"/>
</fig>
<fig id="F4" position="float">
<label>FIGURE 4</label>
<caption>
<p>
<bold>(A)</bold> Spectral representation of EOG signals: This graph presents the EOG signal averaged across various subjects and sessions, providing a spectral overview. The <italic>y</italic>-axis quantifies power in decibels (dB), and the <italic>x</italic>-axis represents frequency in Hertz (Hz), spanning from 1&#xa0;Hz to 50&#xa0;Hz. The blue curve indicates the average power spectrum, while the shaded area around this curve illustrates the standard deviation, reflecting variability among subjects and sessions. <bold>(B)</bold> Signal-to-Noise Ratio (SNR) of the corresponding EOG spectrum.</p>
</caption>
<graphic xlink:href="frvir-06-1468971-g004.tif"/>
</fig>
<p>As can be seen from <xref ref-type="fig" rid="F3">Figure 3</xref>, notable power peaks occur at 1.7&#xa0;Hz, 3.3&#xa0;Hz, and 4.9&#xa0;Hz, likely harmonics of the head movements. These findings suggest that head movement information can likely be a confound for EEG features based on delta and theta bands. Similarly, from <xref ref-type="fig" rid="F4">Figure 4</xref> ocular activity exhibits a 1/f spectral roll-off, suggesting that eye movements may also affect lower frequency bands, specifically the delta and theta bands.</p>
<p>Next, we wish to explore the potential of the three different AAR algorithms at removing these two artifact sources. To this end, we utilize the mutual information computed from the processed EEG signal and the temporal series of the EOG and the averaged tri-axes accelerometer signals. A higher mutual information will signal that the artifacts have not been removed and the EEG signal still contains substantial artifactual information embedded in the signal. In turn, lower mutual information values suggest that the artifacts were correctly removed. <xref ref-type="fig" rid="F5">Figure 5</xref> presents the computed mutual information (averaged over the head and eye movement signals) for each of the seven EEG channels. As can be seen, minimal processing showed the highest mutual information, as expected. The RegICA method removed some of the artifacts, while the more complex ASR &#x2b; ICLabel combination resulted in the least amount of mutual information, suggesting the most aggressive removal of artifacts.</p>
<fig id="F5" position="float">
<label>FIGURE 5</label>
<caption>
<p>Comparative analysis of pre-processing algorithms for EEG signals based on mutual information. The bar plots illustrate the average mutual information scores between EEG channels of pre-processed signals and recorded noise signals (EOG and accelerometer signals) for different pre-processing pipelines. The <italic>y</italic>-axis represents the mutual information score, quantifying the dependency between the EEG signals and noise, while the <italic>x</italic>-axis categorizes EEG electrodes. Error bars indicate standard error, reflecting variability among subjects and sessions.</p>
</caption>
<graphic xlink:href="frvir-06-1468971-g005.tif"/>
</fig>
<p>Lastly, <xref ref-type="fig" rid="F6">Figure 6</xref> depicts the EEG Power Spectral Density averaged across channels processed by the Minimal and the ASR &#x2b; ICLabel pipelines. As can be seen, the 1.7&#xa0;Hz, 2.5, and 3.2&#xa0;Hz peaks, likely due to head movements, can be seen with the former, but not the latter. The spectral density above 6&#xa0;Hz, in turn, closely matches in both scenarios.</p>
<fig id="F6" position="float">
<label>FIGURE 6</label>
<caption>
<p>Comparison of power spectral density between Minimal and ASR &#x2b; ICLabel pre-processings methods. The <italic>y</italic>-axis quantifies power density in <inline-formula id="inf28">
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</caption>
<graphic xlink:href="frvir-06-1468971-g006.tif"/>
</fig>
<p>Comparison of the spectra of the two pipelines, Minimal and ASR &#x2b; ICLabel, suggests that the components identified as ocular and motion artifacts, in <xref ref-type="fig" rid="F4">Figures 3</xref>, <xref ref-type="fig" rid="F3">4</xref> respectively, were eliminated by the ASR &#x2b; ICLabel pipeline, but not by the Minimal pipeline. This observation in the spectral domain is consistent with the results obtained from the mutual information measurements.</p>
</sec>
<sec id="s3-2">
<title>3.2 Ablation study II: combination of AARs, epoch size, and feature type</title>
<p>Despite the effective removal of artifacts, AARs can distort the signals. Therefore, we investigated their impact on the useful information related to cybersickness. We compared different combinations of epoch sizes and each AARs for the predictive power of each type of feature. As a figure-of-merit, we employed the correlation measures described in <xref ref-type="sec" rid="s2-6">Section 2.6</xref>, which were calculated between the samples and the associated FMS rating independently for each feature.</p>
<p>
<xref ref-type="fig" rid="F7">Figure 7</xref> presents the Spearman correlation between different features and the FMS scores in the training set. The correlation map shows results for the different AAR methods, feature types, and epoch sizes. As can be seen, PSD and AMP features showed the highest correlations with the Minimal processing pipeline with the 8 and 20&#xa0;s epochs for AMP features and 8-s epochs for PSDs. Moreover, the band and channel coupling measures showed mild to moderate correlation with FMS across various pre-processing scenarios, suggesting their potential complementarity for cybersickness characterization.</p>
<fig id="F7" position="float">
<label>FIGURE 7</label>
<caption>
<p>Comparative analysis of feature type distribution across different pre-processing conditions and epoch sizes, encompassing six distinct feature types: AMP, PSD, AM-CCPL, CCPL, AM-BCPL, and BCPL. The color intensity within the heatmap denotes the magnitude of the average correlation between data of selected features and FMS ratings.</p>
</caption>
<graphic xlink:href="frvir-06-1468971-g007.tif"/>
</fig>
<p>Overall, the RegICA and ASR &#x2b; ICLabel AAR methods showed lower correlation scores with FMS ratings across most epoch sizes and feature types, whereas the Minimal pre-processing showed the highest. These findings suggest that, indeed, retaining artifacts related to blinks, eye movements, and head movements can be useful to characterize the multimodal effects of cybersickness.</p>
</sec>
<sec id="s3-3">
<title>3.3 Ablation study III: feature selection</title>
<p>Next, we explore the selection of the optimal number of features. <xref ref-type="fig" rid="F8">Figure 8</xref> shows the coefficient of determination <inline-formula id="inf29">
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<fig id="F8" position="float">
<label>FIGURE 8</label>
<caption>
<p>Performance metrics for the ASR &#x2b; ICLabel pre-processing method over a 5-s epoch, as a function of feature count. The graph illustrates the variation of coefficient of determination <inline-formula id="inf32">
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</caption>
<graphic xlink:href="frvir-06-1468971-g008.tif"/>
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<table-wrap id="T1" position="float">
<label>TABLE 1</label>
<caption>
<p>Optimal number of features selected for each combination of epoch sizes and pre-processing techniques. The maximum number of features is set (empirically) to 100 to prevent overfitting.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="center">Epoch size</th>
<th align="center">Minimal</th>
<th align="center">REGICA</th>
<th align="center">ASR &#x2b; ICLabel</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="center">2</td>
<td align="center">100</td>
<td align="center">23</td>
<td align="center">67</td>
</tr>
<tr>
<td align="center">5</td>
<td align="center">100</td>
<td align="center">86</td>
<td align="center">100</td>
</tr>
<tr>
<td align="center">8</td>
<td align="center">97</td>
<td align="center">100</td>
<td align="center">73</td>
</tr>
<tr>
<td align="center">20</td>
<td align="center">78</td>
<td align="center">97</td>
<td align="center">100</td>
</tr>
<tr>
<td align="center">30</td>
<td align="center">81</td>
<td align="center">94</td>
<td align="center">81</td>
</tr>
</tbody>
</table>
</table-wrap>
</sec>
<sec id="s3-4">
<title>3.4 Top-features analysis</title>
<p>To gain greater insight into cybersickness characterization, two analyses were performed based on the interpretation of the most relevant features. The first analysis explores the neural patterns indicative of cybersickness, while the second investigates the multi-modal potential of cybersickness detection with minimal EEG pre-processing.</p>
<p>We employed a strategy to summarize the multiple lists of top features generated for each combination of the AAR algorithm and epoch size. For each AAR, a unified list was created by gathering all features that appeared in at least one of the lists across various epoch sizes. A common list is then defined as the intersection of two unified lists, meaning that a feature must be present in both lists to be included. Therefore, the analysis in the discussion section is based on common features between the two AARs, regardless of the epoch size.</p>
<sec id="s3-4-1">
<title>3.4.1 Neurological patterns associated with cybersickness</title>
<p>For this analysis, the underlying assumption is that the common top-ranked features selected with and without pre-processing will most likely convey details about the neural underpinnings associated with cybersickness. Based on the ablation studies, we use the &#x2018;ASR &#x2b; ICLabel&#x2019; and the &#x2018;Minimal&#x2019; pre-processing methods in this analysis. It was found that the common/overlapped top features list comprised 51 features with 22 accounting for AMP and PSD; 11 for inter-channel coupling features; and 18 for inter-band coupling features. More details about these top features are given next.</p>
<sec id="s3-4-1-1">
<title>3.4.1.1 PSD and AM power features</title>
<p>
<xref ref-type="fig" rid="F9">Figure 9</xref> shows the average correlation with FMS ratings of the top-22 common features from the AMP and PSD categories. In the figure, the electrode locations and feature types are detailed in the <italic>x</italic>-axis labels, while the frequency bands are color-coded. Spatially, the neuronal patterns correlated with cybersickness form two distinct clusters: alpha-mtheta, alpha, and theta bands are prevalent in the parietal (P3, P4, Pz) and centro-parietal (CP5, CP6) areas, while alpha-mdelta, delta, and beta-mdelta bands are primarily observed in the central (Cz) and frontal (Fz) regions.</p>
<fig id="F9" position="float">
<label>FIGURE 9</label>
<caption>
<p>Bar plot representing average correlation between overlapped AMP and PSD features and FMS ratings. The feature types and EEG electrodes are described on the <italic>x</italic>-axis, while the corresponding frequency bands are color-coded (see the figure legend).</p>
</caption>
<graphic xlink:href="frvir-06-1468971-g009.tif"/>
</fig>
<p>The average AM power (AMP_mean) primarily consists of alpha-mtheta frequencies, while the average band power (PSD_mean) is mainly characterized by theta and alpha frequencies. Notably, theta oscillations are more significant when their average power across an entire minute is taken, indicating their role as a persistent process.</p>
<p>Moreover, the variability in power, as indicated by the standard deviation features (AMP_std and PSD_std), is most closely associated with the alpha-mdelta and alpha bands, respectively. The observed increase in the variability of alpha-mdelta band power, taken over a 1-min window indicate instability of the alpha band slow temporal dynamic as the perceived cybersickness symptoms increase. This feature may reflect neuronal mechanisms capable of flexible and adaptive responses to cybersickness.</p>
<p>Next, we take a more in-depth look at the two features with the highest correlation with FMS in <xref ref-type="fig" rid="F9">Figure 9</xref>, namely, mean alpha-mtheta at CP6 and the standard deviation of alpha-mdelta power at CP5. As can be seen in <xref ref-type="fig" rid="F10">Figure 10</xref>, the average alpha-mtheta activity and the alpha-mdelta power standard deviation exhibits a significant positive correlation with FMS ratings. Notably, variability among participants is increased within the 0.5-1 normalized FMS score range, suggesting a more unstable/inconsistent pattern across this interval.</p>
<fig id="F10" position="float">
<label>FIGURE 10</label>
<caption>
<p>Lateral Parietal Grand average feature values of AMP_mean_alpha-mtheta_CP6 and AMP_std_alpha-mdelta_CP5 versus FMS ratings using the ASR &#x2b; ICLabel pre-processed dataset. The grand average was calculated by grouping individual subject ratings, averaging them within subjects, and then averaging these values across all subjects to obtain a unified measure for each feature. Both features show a significant positive correlation. The filled areas correspond to standard errors around each curve. Coefficients marked with &#x2a; and &#x2a;&#x2a; represent the Pearson correlation between the grand average and FMS ratings with a p-value <inline-formula id="inf34">
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<p>
<xref ref-type="fig" rid="F11">Figure 11</xref>, in turn, depicts the temporal changes of the two features over the 10-min experiment which exhibited increased cybersickness levels over time. As can be seen, both features exhibited a significant increase over time, suggesting they may serve as a precursor to predict the onset of cybersickness, with symptomatic manifestation becoming consistently evident across participants only after they have been exposed to VR for an extended period. Moreover, it is important to highlight that the variability across subjects (represented by the shaded bands) increased towards the end of the experiment, likely attributed to the reduced amount of data available for accurate standard deviation estimation, as not all participants reached the end of the experiment due to nausea symptoms.</p>
<fig id="F11" position="float">
<label>FIGURE 11</label>
<caption>
<p>Lateral Parietal Grand average feature value of AMP_mean_alpha-mtheta_CP6 (blue curve) and AMP_std_alpha-mdelta_CP5 (orange curve) as a function of time using ASR &#x2b; ICLabel pre-processed dataset with 5&#xa0;s epoch size. Both features show an increase over time, suggesting potential tracking of cybersickness levels. The filled area corresponds to the standard error around each curves. Coefficients marked with &#x2a;&#x2a;&#x2a; represent the Pearson correlation with a p-value <inline-formula id="inf36">
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<mml:mo>&#x3c;</mml:mo>
<mml:mn>0.001</mml:mn>
</mml:mrow>
</mml:math>
</inline-formula> between grand average and time stamps.</p>
</caption>
<graphic xlink:href="frvir-06-1468971-g011.tif"/>
</fig>
</sec>
<sec id="s3-4-1-2">
<title>3.4.1.2 Inter-channel coupling features</title>
<p>
<xref ref-type="fig" rid="F12">Figure 12</xref> depicts the average correlation between data from CCPL based features and FMS ratings. As observed, the most relevant pattern appears to be associated with the beta band. Both average and standard deviation power exhibit similar correlations with cybersickness, specifically with beta-mtheta and beta for AM-CCPL and CCPL, respectively. Channel coupling seems to predominantly occur in centro-parietal (channels Cz, CP5, CP6) and parietal regions (channels P3, Pz, P4). The predominance of centro-parietal activity correlated with FMS ratings suggests involvement in proprioceptive processes, visual/sensorial stimulus processing, and the integration of contextual information (<xref ref-type="bibr" rid="B8">Albanese et al., 2023</xref>; <xref ref-type="bibr" rid="B148">Walter and Dassonville, 2008</xref>; <xref ref-type="bibr" rid="B138">Summerfield and Mangels, 2005</xref>) during cybersickness.</p>
<fig id="F12" position="float">
<label>FIGURE 12</label>
<caption>
<p>Bar plot representing average correlation between overlapped CCPL features and FMS ratings. The feature subtype and coupled channel pairs are described in the <italic>x</italic>-axis, while the corresponding frequency bands are color coded (see figure legend).</p>
</caption>
<graphic xlink:href="frvir-06-1468971-g012.tif"/>
</fig>
<p>Moreover, the figure reveals a significant pattern of coupling within the beta-mtheta band, evidenced by features such as AM_ccor_mean CP5 &#xd7; CP6 and AM_ccor_std Pz &#xd7; Cz. This pattern emphasizes the crucial role of the beta band in mediating interactions between various cortical areas.</p>
</sec>
<sec id="s3-4-1-3">
<title>3.4.1.3 Inter-band coupling features</title>
<p>
<xref ref-type="fig" rid="F13">Figure 13</xref> depicts the average correlations between data from inter-band coupling features and FMS ratings. Within BCPL features only two features appeared in the top: an average decoupling is observed between theta and gamma in left Parietal area (channel P3) whereas a strong coupling variability occurs between theta and beta band in left centro-parietal area (channel CP5).</p>
<fig id="F13" position="float">
<label>FIGURE 13</label>
<caption>
<p>Bar plot representing average correlation between overlapped BCPL features data and FMS ratings. The feature subtype and coupled band pairs are described in the <italic>x</italic>-axis, while the corresponding channels are color coded (see figure legend).</p>
</caption>
<graphic xlink:href="frvir-06-1468971-g013.tif"/>
</fig>
<p>AM-BCPL features are, in turn, predominant in the top feature list. As can be seen, activities correlated with cybersickness intensity are observed in multiples cortical regions with alpha and beta band couplings in the midline electrodes (Fz, Cz and Pz) represented by features alpha-mdelta<inline-formula id="inf39">
<mml:math id="m39">
<mml:mrow>
<mml:mo>&#xd7;</mml:mo>
</mml:mrow>
</mml:math>
</inline-formula>beta-mdelta and alpha-mdelta<inline-formula id="inf40">
<mml:math id="m40">
<mml:mrow>
<mml:mo>&#xd7;</mml:mo>
</mml:mrow>
</mml:math>
</inline-formula>beta-mbeta. In the centro-parietal region, increased coupling is observed in bilateral parietal area between gamma-mtheta and beta-mdelta (P4) and gamma-malpha (P3), accompanied by decoupling within the beta band: beta-mtheta<inline-formula id="inf41">
<mml:math id="m41">
<mml:mrow>
<mml:mo>&#xd7;</mml:mo>
</mml:mrow>
</mml:math>
</inline-formula>beta-malpha (Pz, P4).</p>
<p>The frontal lobe (channel Fz), like the centro-parietal area, seems to be particularly important in the coupling between frequency bands. A notable decoupling between gamma and alpha bands, represented by the feature alpha-mtheta<inline-formula id="inf42">
<mml:math id="m42">
<mml:mrow>
<mml:mo>&#xd7;</mml:mo>
</mml:mrow>
</mml:math>
</inline-formula>gamma-malpha, is concurrently observed with an increase in coupling within the temporal structure of both beta and gamma bands represented by the features gamma-mdelta<inline-formula id="inf43">
<mml:math id="m43">
<mml:mrow>
<mml:mo>&#xd7;</mml:mo>
</mml:mrow>
</mml:math>
</inline-formula>gamma-mtheta and beta-mdelta<inline-formula id="inf44">
<mml:math id="m44">
<mml:mrow>
<mml:mo>&#xd7;</mml:mo>
</mml:mrow>
</mml:math>
</inline-formula>beta-mtheta. Taking gamma as an example, gamma-mdelta and gamma-mtheta bands measure the slowest changes in the instantaneous amplitude of the band. The increased coupling between these two bands can be interpreted as the progressive homogenization of the long time scale structure of gamma oscillations.</p>
<p>Overall, the prevalent patterns involve the average coupling of the modulated beta band with alpha and gamma bands, suggesting that the beta band may act as a conduit between slow and rapid neuronal activities during cybersickness episodes. Furthermore, the coupling between beta-mtheta and beta-malpha can be identified as a significant pattern associated with cybersickness. Theta and alpha bands appear to engage in a common neuronal mechanism that modulates the amplitude of fast oscillations, notably within the beta band. According to the top-down theory (<xref ref-type="bibr" rid="B118">Richter et al., 2017</xref>), this modulation could be attributed to changes in activity within local neuronal assemblies&#x2013;represented by fast oscillations&#x2013;under the remote control of deeper brain structures through slower waves.</p>
<p>The manifestation of coupling related to the beta band, both spatially across centro-parietal channels (Cz, CP5, CP6, Pz) and spectrally between the beta-mtheta and beta-malpha bands, highlights the beta band&#x2019;s central role in facilitating the dynamic formation and integration of cortical networks under cybersickness conditions.</p>
<p>The negative correlation between cybersickness severity and the coupling between beta-mtheta and beta-malpha indicates a diminishing interaction between their respective cortical processes as cybersickness intensifies, as depicted by <xref ref-type="fig" rid="F14">Figures 14</xref>, <xref ref-type="fig" rid="F15">15</xref>. It could be argued that increased presence of artifacts affecting the theta band with rising cybersickness levels, could lead to a decoupling. However, the temporal progression of both beta-mtheta and beta-malpha, shown in <xref ref-type="fig" rid="F16">Figure 16</xref>, exhibits a significant increase over time. The increase is also observed in the P4 electrode, although not significant, as illustrated in <xref ref-type="fig" rid="F17">Figure 17</xref>. Furthermore, the similar correlation values of &#x2212;0.31 and &#x2212;0.29 for the Minimal and ASR &#x2b; ICLabel pipelines, respectively, suggest that the decoupling between beta-mtheta and beta-malpha bands is not primarily due to artifacts.</p>
<fig id="F14" position="float">
<label>FIGURE 14</label>
<caption>
<p>Right Parietal Grand average feature value of AMP_mean_beta-malpha_P4 (blue), AMP_mean_beta-mtheta_P4 (orange) and AM_bcor_mean_P4_beta-mtheta_beta-malpha (green) across recordings as a function of normalized FMS ratings using ASR &#x2b; ICLabel pre-processed dataset with 5&#xa0;s epoch size. A strong significant negative correlation is observed with AM_bcor_mean_P4_beta-mtheta_beta-malpha. Coefficients marked with &#x2a; and n.s. represent the Pearson correlation between grand average and FMS ratings with a p-value <inline-formula id="inf45">
<mml:math id="m45">
<mml:mrow>
<mml:mo>&#x3c;</mml:mo>
<mml:mn>0.05</mml:mn>
</mml:mrow>
</mml:math>
</inline-formula> and non-significance, respectively.</p>
</caption>
<graphic xlink:href="frvir-06-1468971-g014.tif"/>
</fig>
<fig id="F15" position="float">
<label>FIGURE 15</label>
<caption>
<p>Parietal Grand average feature value of AMP_mean_beta-malpha_Pz (blue), AMP_mean_beta-mtheta_Pz (orange) and AM_bcor_mean_Pz_beta-mtheta_beta-malpha (green) across subjects and sessions as a function of normalized FMS ratings using ASR &#x2b; ICLabel pre-processed dataset. A strong significant negative correlation is observed with AM_bcor_mean_Pz_beta-mtheta_beta-malpha. Coefficients marked with &#x2a;&#x2a; and n.s. represent the Pearson correlation between grand average and FMS ratings with a p-value <inline-formula id="inf46">
<mml:math id="m46">
<mml:mrow>
<mml:mo>&#x3c;</mml:mo>
<mml:mn>0.01</mml:mn>
</mml:mrow>
</mml:math>
</inline-formula> and non significance respectively.</p>
</caption>
<graphic xlink:href="frvir-06-1468971-g015.tif"/>
</fig>
<fig id="F16" position="float">
<label>FIGURE 16</label>
<caption>
<p>Parietal Grand average feature value of AMP_mean_beta-malpha_Pz (blue), AMP_mean_beta-mtheta_Pz (orange) and AM_bcor_mean_Pz_beta-mtheta_beta-malpha (green) across subjects and sessions as a function of time using ASR &#x2b; ICLabel pre-processed dataset. Both power beta-malpha and beta-mtheta features show a significant strong positive correlation with time. Coefficients marked with &#x2a;&#x2a;, &#x2a; and n.s. represent the Pearson correlation between grand average and FMS ratings with a p-value <inline-formula id="inf47">
<mml:math id="m47">
<mml:mrow>
<mml:mo>&#x3c;</mml:mo>
<mml:mn>0.01</mml:mn>
</mml:mrow>
</mml:math>
</inline-formula>, p-value <inline-formula id="inf48">
<mml:math id="m48">
<mml:mrow>
<mml:mo>&#x3c;</mml:mo>
<mml:mn>0.05</mml:mn>
</mml:mrow>
</mml:math>
</inline-formula> and non significance, respectively.</p>
</caption>
<graphic xlink:href="frvir-06-1468971-g016.tif"/>
</fig>
<fig id="F17" position="float">
<label>FIGURE 17</label>
<caption>
<p>Right Parietal Grand average feature value of AMP_mean_beta-malpha_P4 (blue), AMP_mean_beta-mtheta_P4 (orange) and AM_bcor_mean_P4_beta-mtheta_beta-malpha (green) across recordings as a function of time using ASR &#x2b; ICLabel pre-processed dataset. Both power beta-malpha and beta-mtheta features show a weak positive correlation with time. Coefficients represent the Pearson correlation between grand average and FMS ratings. None of the correlations were significant as indicated by n.s.</p>
</caption>
<graphic xlink:href="frvir-06-1468971-g017.tif"/>
</fig>
<p>Additionally, both bands display a similarly weak, non-significant correlation with FMS ratings for both channels P4 and Pz, as illustrated in <xref ref-type="fig" rid="F14">Figures 14</xref>, <xref ref-type="fig" rid="F15">15</xref>. Considering the absence of a significant correlation with FMS ratings, the observed decoupling between beta-mtheta and beta-malpha bands is unlikely to stem from direct changes in power within either band. Instead, this pattern underscores a more complex interaction, suggesting a dynamic rerouting or reorganization of the cortical network as an adaptive response to cybersickness. This observation support the robustness of AM-based features in extracting meaningful patterns regardless of the presence of artifacts.</p>
</sec>
</sec>
<sec id="s3-4-2">
<title>3.4.2 EEG-based embedding of multiple modalities and their role in cybersickness prediction</title>
<p>As mentioned previously, minimal pre-processing of the EEG signal leaves several artifacts within the EEG time series that may be useful for cybersickness prediction, such as eye and head movements. In this analysis, we take an in-depth look at the top-features selected with the Minimal pre-processing pipeline that did not overlap with those selected from the other two more complex pre-processing methods. The top-features were selected based on their prevalence within the top feature lists across at least three out of five epoch sizes tested within the Minimal pre-processing condition.</p>
<p>
<xref ref-type="fig" rid="F18">Figure 18</xref> shows the top PSD and AM power-based features, which accounted to 23 of the 44 top features. As can be seen, the correlation values are higher than those reported from the previous analysis. Moreover, a marked increase in the occurrence of the delta and theta band features is shown, especially around the central and parietal regions (channels Cz, CP5, CP6, P3, Pz, P4). As was discussed in <xref ref-type="sec" rid="s3-1">Section 3.1</xref>, these bands tend to be more sensitive to head and eye movements artifacts, thus may be encoding such details.</p>
<fig id="F18" position="float">
<label>FIGURE 18</label>
<caption>
<p>Bar plot representing average correlation between feature data and FMS ratings from the top features list using Minimal pre-processing method. Some features overlap with those from the ASR &#x2b; ICLabel preprocessing. Only the AMP and PSD features are represented. The feature type and EEG electrodes are described in the <italic>x</italic>-axis, while the corresponding frequency bands are color coded (see figure legend).</p>
</caption>
<graphic xlink:href="frvir-06-1468971-g018.tif"/>
</fig>
<p>Comparing <xref ref-type="fig" rid="F18">Figure 18</xref> with <xref ref-type="fig" rid="F9">Figure 9</xref>, the presence of delta and theta bands in the latter remains limited. This is likely due to contamination by ocular and movement artifacts preserved by Minimal pipeline but removed by ASR &#x2b; ICLabel. Notwithstanding, the previous analysis also showed the presence of theta band activity within the top features that overlapped the ASR &#x2b; ICLabel and Minimal pre-processing approaches, thus suggesting that theta-band patterns may not be entirely attributed to artifacts, but may also convey some neurological origin related to cybersickness.</p>
<p>
<xref ref-type="table" rid="T2">Table 2</xref> shows the remaining top-21 features (out of total 44) from the CCPL and BCPL feature categories. As can be seen, the majority of the top features correspond to band coupling between amplitude modulated bands. The most recurring carrier band is gamma followed by beta, while the most recurring modulator band is theta.</p>
<table-wrap id="T2" position="float">
<label>TABLE 2</label>
<caption>
<p>Top-selected coupling features (BCPL, CCPL, AM-BCPL and AM-CCPL) identified using Minimal pre-processing across different epoch durations (2, 5, 8, 20, and 30&#xa0;s).</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="center">Feature type</th>
<th align="center">Band</th>
<th align="center">Channel</th>
<th align="center">Mean absolute correlation</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="center">beta</td>
<td align="center">CCPL_std</td>
<td align="center">Pz<inline-formula id="inf49">
<mml:math id="m49">
<mml:mrow>
<mml:mo>&#xd7;</mml:mo>
</mml:mrow>
</mml:math>
</inline-formula>P3</td>
<td align="center">0.34</td>
</tr>
<tr>
<td align="center">gamma-mtheta<inline-formula id="inf50">
<mml:math id="m50">
<mml:mrow>
<mml:mo>&#xd7;</mml:mo>
</mml:mrow>
</mml:math>
</inline-formula>gamma-malpha</td>
<td align="center">AM_BCPL_mean</td>
<td align="center">Fz</td>
<td align="center">0.34</td>
</tr>
<tr>
<td align="center">beta-malpha<inline-formula id="inf51">
<mml:math id="m51">
<mml:mrow>
<mml:mo>&#xd7;</mml:mo>
</mml:mrow>
</mml:math>
</inline-formula>beta-mbeta</td>
<td align="center">AM_BCPL_mean</td>
<td align="center">P4</td>
<td align="center">0.33</td>
</tr>
<tr>
<td align="center">alpha-mtheta<inline-formula id="inf52">
<mml:math id="m52">
<mml:mrow>
<mml:mo>&#xd7;</mml:mo>
</mml:mrow>
</mml:math>
</inline-formula>gamma-mbeta</td>
<td align="center">AM_BCPL_mean</td>
<td align="center">Fz</td>
<td align="center">0.33</td>
</tr>
<tr>
<td align="center">gamma-mtheta<inline-formula id="inf53">
<mml:math id="m53">
<mml:mrow>
<mml:mo>&#xd7;</mml:mo>
</mml:mrow>
</mml:math>
</inline-formula>gamma-malpha</td>
<td align="center">AM_BCPL_mean</td>
<td align="center">Pz</td>
<td align="center">0.32</td>
</tr>
<tr>
<td align="center">gamma-mbeta<inline-formula id="inf54">
<mml:math id="m54">
<mml:mrow>
<mml:mo>&#xd7;</mml:mo>
</mml:mrow>
</mml:math>
</inline-formula>gamma-mgamma</td>
<td align="center">AM_BCPL_mean</td>
<td align="center">P3</td>
<td align="center">0.32</td>
</tr>
<tr>
<td align="center">gamma-mdelta<inline-formula id="inf55">
<mml:math id="m55">
<mml:mrow>
<mml:mo>&#xd7;</mml:mo>
</mml:mrow>
</mml:math>
</inline-formula>gamma-malpha</td>
<td align="center">AM_BCPL_mean</td>
<td align="center">Pz</td>
<td align="center">0.32</td>
</tr>
<tr>
<td align="center">theta-mtheta<inline-formula id="inf56">
<mml:math id="m56">
<mml:mrow>
<mml:mo>&#xd7;</mml:mo>
</mml:mrow>
</mml:math>
</inline-formula>gamma-mbeta</td>
<td align="center">AM_BCPL_mean</td>
<td align="center">Cz</td>
<td align="center">0.32</td>
</tr>
<tr>
<td align="center">gamma-mtheta<inline-formula id="inf57">
<mml:math id="m57">
<mml:mrow>
<mml:mo>&#xd7;</mml:mo>
</mml:mrow>
</mml:math>
</inline-formula>gamma-malpha</td>
<td align="center">AM_BCPL_mean</td>
<td align="center">P3</td>
<td align="center">0.32</td>
</tr>
<tr>
<td align="center">theta-mtheta<inline-formula id="inf58">
<mml:math id="m58">
<mml:mrow>
<mml:mo>&#xd7;</mml:mo>
</mml:mrow>
</mml:math>
</inline-formula>gamma-mbeta</td>
<td align="center">AM_BCPL_mean</td>
<td align="center">P3</td>
<td align="center">0.31</td>
</tr>
<tr>
<td align="center">gamma-mdelta<inline-formula id="inf59">
<mml:math id="m59">
<mml:mrow>
<mml:mo>&#xd7;</mml:mo>
</mml:mrow>
</mml:math>
</inline-formula>gamma-mtheta</td>
<td align="center">AM_BCPL_mean</td>
<td align="center">CP6</td>
<td align="center">0.31</td>
</tr>
<tr>
<td align="center">beta-mdelta<inline-formula id="inf60">
<mml:math id="m60">
<mml:mrow>
<mml:mo>&#xd7;</mml:mo>
</mml:mrow>
</mml:math>
</inline-formula>beta-mtheta</td>
<td align="center">AM_BCPL_mean</td>
<td align="center">CP6</td>
<td align="center">0.31</td>
</tr>
<tr>
<td align="center">beta-mtheta<inline-formula id="inf61">
<mml:math id="m61">
<mml:mrow>
<mml:mo>&#xd7;</mml:mo>
</mml:mrow>
</mml:math>
</inline-formula>beta-malpha</td>
<td align="center">AM_BCPL_mean</td>
<td align="center">P4</td>
<td align="center">0.31</td>
</tr>
<tr>
<td align="center">beta-malpha<inline-formula id="inf62">
<mml:math id="m62">
<mml:mrow>
<mml:mo>&#xd7;</mml:mo>
</mml:mrow>
</mml:math>
</inline-formula>beta-mbeta</td>
<td align="center">AM_BCPL_mean</td>
<td align="center">P3</td>
<td align="center">0.31</td>
</tr>
<tr>
<td align="center">gamma-mtheta<inline-formula id="inf63">
<mml:math id="m63">
<mml:mrow>
<mml:mo>&#xd7;</mml:mo>
</mml:mrow>
</mml:math>
</inline-formula>gamma-mbeta</td>
<td align="center">AM_BCPL_std</td>
<td align="center">Fz</td>
<td align="center">0.31</td>
</tr>
<tr>
<td align="center">gamma-mtheta<inline-formula id="inf64">
<mml:math id="m64">
<mml:mrow>
<mml:mo>&#xd7;</mml:mo>
</mml:mrow>
</mml:math>
</inline-formula>gamma-malpha</td>
<td align="center">AM_BCPL_mean</td>
<td align="center">CP6</td>
<td align="center">0.31</td>
</tr>
<tr>
<td align="center">gamma-mdelta<inline-formula id="inf65">
<mml:math id="m65">
<mml:mrow>
<mml:mo>&#xd7;</mml:mo>
</mml:mrow>
</mml:math>
</inline-formula>gamma-malpha</td>
<td align="center">AM_BCPL_mean</td>
<td align="center">P3</td>
<td align="center">0.30</td>
</tr>
<tr>
<td align="center">gamma-mbeta<inline-formula id="inf66">
<mml:math id="m66">
<mml:mrow>
<mml:mo>&#xd7;</mml:mo>
</mml:mrow>
</mml:math>
</inline-formula>gamma-mgamma</td>
<td align="center">AM_BCPL_std</td>
<td align="center">CP5</td>
<td align="center">0.30</td>
</tr>
<tr>
<td align="center">gamma-mdelta<inline-formula id="inf67">
<mml:math id="m67">
<mml:mrow>
<mml:mo>&#xd7;</mml:mo>
</mml:mrow>
</mml:math>
</inline-formula>gamma-mtheta</td>
<td align="center">AM_BCPL_mean</td>
<td align="center">P3</td>
<td align="center">0.30</td>
</tr>
<tr>
<td align="center">beta-mdelta</td>
<td align="center">AM_CCPL_std</td>
<td align="center">Pz<inline-formula id="inf68">
<mml:math id="m68">
<mml:mrow>
<mml:mo>&#xd7;</mml:mo>
</mml:mrow>
</mml:math>
</inline-formula>P3</td>
<td align="center">0.29</td>
</tr>
<tr>
<td align="center">beta-mbeta<inline-formula id="inf69">
<mml:math id="m69">
<mml:mrow>
<mml:mo>&#xd7;</mml:mo>
</mml:mrow>
</mml:math>
</inline-formula>gamma-mgamma</td>
<td align="center">AM_BCPL_mean</td>
<td align="center">P4</td>
<td align="center">0.29</td>
</tr>
</tbody>
</table>
</table-wrap>
</sec>
</sec>
<sec id="s3-5">
<title>3.5 Overall cybersickness characterization</title>
<p>
<xref ref-type="table" rid="T3">Table 3</xref> lists the final RMSE achieved between the real (normalized) FMS ratings and the predicted ones for each pre-processing strategy and epoch size. These results reflect the model&#x2019;s performance on unseen data, as the training and testing folds used in cross-validation are strictly non-overlapping. To gauge the significance of the results in the table over chance, a random classifier is also trained where the FMS ratings, which serve as regression labels, are randomized. As can be seen, across all tested configurations, performance significantly exceeded this chance level. <xref ref-type="table" rid="T4">Table 4</xref> summarizes the main relevant features used for cybersickness level measurement.</p>
<table-wrap id="T3" position="float">
<label>TABLE 3</label>
<caption>
<p>RMSE values derived from a 5-fold cross-validation regression analysis, assessing the impact of various pre-processing techniques over different epoch durations on regression performance. The benchmark for random performance was established through successive permutation tests and random FMS ratings. Entries significantly surpassing this benchmark (p <inline-formula id="inf70">
<mml:math id="m70">
<mml:mrow>
<mml:mo>&#x3c;</mml:mo>
<mml:mn>0.05</mml:mn>
</mml:mrow>
</mml:math>
</inline-formula>) are denoted by an asterisk (&#x2a;). Lower RMSE values, indicative of best model prediction across epoch sizes, are emphasized in bold for each pre-processing condition.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="center"/>
<th colspan="2" align="center">Minimal</th>
<th colspan="2" align="center">REGICA</th>
<th colspan="2" align="center">ASR &#x2b; ICLabel</th>
</tr>
<tr>
<th align="center">Epoch size</th>
<th align="center">Score</th>
<th align="center">Random</th>
<th align="center">Score</th>
<th align="center">Random</th>
<th align="center">Score</th>
<th align="center">Random</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="center">2</td>
<td align="center">0.253&#x2a;</td>
<td align="center">0.333</td>
<td align="center">0.268&#x2a;</td>
<td align="center">0.337</td>
<td align="center">0.254&#x2a;</td>
<td align="center">0.32</td>
</tr>
<tr>
<td align="center">5</td>
<td align="center">0.246&#x2a;</td>
<td align="center">0.331</td>
<td align="center">0.249&#x2a;</td>
<td align="center">0.323</td>
<td align="center">
<bold>0.247&#x2a;</bold>
</td>
<td align="center">0.327</td>
</tr>
<tr>
<td align="center">8</td>
<td align="center">
<bold>0.234&#x2a;</bold>
</td>
<td align="center">0.327</td>
<td align="center">0.262&#x2a;</td>
<td align="center">0.326</td>
<td align="center">0.254&#x2a;</td>
<td align="center">0.327</td>
</tr>
<tr>
<td align="center">20</td>
<td align="center">0.258&#x2a;</td>
<td align="center">0.327</td>
<td align="center">0.248&#x2a;</td>
<td align="center">0.327</td>
<td align="center">0.248&#x2a;</td>
<td align="center">0.309</td>
</tr>
<tr>
<td align="center">30</td>
<td align="center">0.25&#x2a;</td>
<td align="center">0.324</td>
<td align="center">
<bold>0.245&#x2a;</bold>
</td>
<td align="center">0.329</td>
<td align="center">0.257&#x2a;</td>
<td align="center">0.332</td>
</tr>
</tbody>
</table>
</table-wrap>
<table-wrap id="T4" position="float">
<label>TABLE 4</label>
<caption>
<p>Summary of relevant features for cybersickness measurement.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="left">Type</th>
<th align="left">Function</th>
<th align="left">Channel</th>
<th align="left">Band</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left">PSD</td>
<td align="left">Mean</td>
<td align="left">CP6</td>
<td align="left">Alpha-mTheta</td>
</tr>
<tr>
<td align="left">PSD</td>
<td align="left">Std</td>
<td align="left">CP5</td>
<td align="left">Alpha-mDelta</td>
</tr>
<tr>
<td align="left">PSD</td>
<td align="left">Mean</td>
<td align="left">P3</td>
<td align="left">Alpha</td>
</tr>
<tr>
<td align="left">PSD</td>
<td align="left">Std</td>
<td align="left">Pz</td>
<td align="left">Alpha</td>
</tr>
<tr>
<td align="left">AM</td>
<td align="left">Mean</td>
<td align="left">P4</td>
<td align="left">Beta-mDelta</td>
</tr>
<tr>
<td align="left">AM</td>
<td align="left">Std</td>
<td align="left">Pz</td>
<td align="left">Beta-mTheta</td>
</tr>
<tr>
<td align="left">AM</td>
<td align="left">Mean</td>
<td align="left">P3</td>
<td align="left">Gamma-mTheta</td>
</tr>
<tr>
<td align="left">AM</td>
<td align="left">Mean</td>
<td align="left">Fz</td>
<td align="left">Gamma-mBeta</td>
</tr>
<tr>
<td align="left">AM-BCPL</td>
<td align="left">Mean</td>
<td align="left">Fz</td>
<td align="left">Alpha-mTheta &#xd7; Gamma-mBeta</td>
</tr>
<tr>
<td align="left">AM-BCPL</td>
<td align="left">Std</td>
<td align="left">Pz</td>
<td align="left">Beta-mTheta &#xd7; Beta-mAlpha</td>
</tr>
<tr>
<td align="left">AM-BCPL</td>
<td align="left">Mean</td>
<td align="left">CP6</td>
<td align="left">Gamma-mDelta &#xd7; Gamma-mTheta</td>
</tr>
<tr>
<td align="left">AM-CCPL</td>
<td align="left">Mean</td>
<td align="left">Cz &#xd7; CP6</td>
<td align="left">Beta</td>
</tr>
<tr>
<td align="left">CCPL</td>
<td align="left">Std</td>
<td align="left">Pz &#xd7; P3</td>
<td align="left">Beta</td>
</tr>
<tr>
<td align="left">BCPL</td>
<td align="left">Mean</td>
<td align="left">P4</td>
<td align="left">Theta &#xd7; Gamma</td>
</tr>
</tbody>
</table>
</table-wrap>
<p>Overall, the &#x2018;Minimal&#x2019; pre-processing approach achieved the lowest RMSE values with top features computed from 8-s epochs, achieving an RMSE of 0.234, significantly lower than chance-level (0.327), corroborating the importance of the multi-modal aspect achieved by leaving artifacts untouched. In contrast, the RegICA and ASR &#x2b; ICLabel pre-processing approaches achieved their lowest RMSE values at higher epoch sizes. As these methods tend to remove artifacts, the regressors are relying solely on neural signatures for cybersickness prediction. In such cases, the longer duration epochs are needed to capture the neural underpinnings of cybersickness, which may be present in lower-frequency activity.</p>
</sec>
</sec>
<sec sec-type="discussion" id="s4">
<title>4 Discussion</title>
<p>In this study, we started with two main objectives: (1) to better understand the impact of artifact removal on EEG-based cybersickness prediction, and (2) to obtain more insights on the neural underpinnings of cybersickness via the use of new amplitude modulation features. Via a series of ablation studies, correlation analyses, and top-feature evaluations, our experiments have provided cues into these two objectives. In the subsequent sections, we discuss these findings in more detail.</p>
<sec id="s4-1">
<title>4.1 To pre-process or not to pre-process?</title>
<p>In EEG studies, the presence of artifacts can negatively influence the validity and interpretation of results (<xref ref-type="bibr" rid="B158">Zhou et al., 2023</xref>; <xref ref-type="bibr" rid="B93">Lopes et al., 2023</xref>; <xref ref-type="bibr" rid="B20">Bennett et al., 2021</xref>), as artifacts can take on various forms (<xref ref-type="bibr" rid="B40">Delorme, 2023</xref>; <xref ref-type="bibr" rid="B98">Michel and Brunet, 2019</xref>; <xref ref-type="bibr" rid="B73">Jin et al., 2023</xref>) and overlap with neurological signals in spatial, temporal and spectral domains (<xref ref-type="bibr" rid="B143">Thompson et al., 2008</xref>; <xref ref-type="bibr" rid="B36">Chiarion et al., 2023</xref>). While this makes the use of pre-processing an essential step in EEG signal analysis, there is no universally accepted method. Algorithms are developed to target certain types of artifacts [e.g. (<xref ref-type="bibr" rid="B120">Robbins et al., 2020</xref>; <xref ref-type="bibr" rid="B155">Yu et al., 2022</xref>)] and each pre-processing method comes with its own set of advantages and limitations. As such, researchers must trade-off between effective artifact removal and minimal signal distortion (<xref ref-type="bibr" rid="B26">Bouazizi and Ltifi, 2024</xref>; <xref ref-type="bibr" rid="B140">Tajmirriahi et al., 2022</xref>; <xref ref-type="bibr" rid="B17">Bao et al., 2022</xref>).</p>
<p>Recently, the extensive use of AAR has been contested due to the excessive data distortions and destruction they might cause to the data (<xref ref-type="bibr" rid="B40">Delorme, 2023</xref>; <xref ref-type="bibr" rid="B36">Chiarion et al., 2023</xref>). For instance, ICA has been shown to produce distortions due to the non-stationary nature of EEG signals (<xref ref-type="bibr" rid="B36">Chiarion et al., 2023</xref>; <xref ref-type="bibr" rid="B26">Bouazizi and Ltifi, 2024</xref>). Additionally, it may mix neurological and non-neurological sources within the same components when the number of channels is much smaller than the number of sources (<xref ref-type="bibr" rid="B143">Thompson et al., 2008</xref>; <xref ref-type="bibr" rid="B139">Sun and Mou, 2023</xref>; <xref ref-type="bibr" rid="B33">Chaddad et al., 2023</xref>), which can often be the case in VR applications.</p>
<p>As with most EEG studies, our results also indicate that non-neurological activity is recorded along with neurological activity. More specifically, we show that ocular activity and head movements are observed in the lower frequencies of the EEG spectrum, such as delta and theta, and these were selected as top-features in the Minimal processing case. In turn, other features from these regions, but measuring temporal dynamics information, could be indicative of regulatory and coordinating roles in cognitive processes.</p>
<p>Unlike other studies, however, for cybersickness prediction, the presence of physiological artifacts can serve as useful sources of multimodal information to predict cybersickness levels (<xref ref-type="bibr" rid="B62">Islam et al., 2021</xref>; <xref ref-type="bibr" rid="B42">Dennison et al., 2016</xref>; <xref ref-type="bibr" rid="B63">Islam et al., 2022</xref>; <xref ref-type="bibr" rid="B35">Chang et al., 2021</xref>; <xref ref-type="bibr" rid="B132">Shimada et al., 2023b</xref>; <xref ref-type="bibr" rid="B68">Jeong et al., 2022</xref>). The obtained findings showed that Minimal processing, indeed, resulted in the lowest cybersickness level prediction error. Therefore, if one is interested in maximizing cybersickness prediction accuracy, performing minimal pre-processing may be the way to go. It is suggested, however, that careful scrutiny of the top-used features be evaluated, to ensure that indeed the developed models are also relying on relevant neural data, and not just physiological artifacts. Furthermore, the main sources of artifacts should be precisely identified when implementing an EEG-embedded multimodal system, as not all artifacts are useful for predictions and may negatively impact outcomes.</p>
</sec>
<sec id="s4-2">
<title>4.2 Cybersickness and neural insights</title>
<sec id="s4-2-1">
<title>4.2.1 Beta band insights</title>
<p>We showed that the features measuring CCPL and AM-CCPL variability in the centro-parietal region (channels Cz, CP5, P3, Pz, P4) within the beta and beta-mtheta bands indicated an increase in coupling variability as the FMS score increased. With the increase in cybersickness symptoms reflected by the FMS score, not only did we observe a decrease in the interaction between distant regions of the parietal area, but their connections also become more unstable.</p>
<p>Although a decrease in beta power is the most recurrent pattern related to cybersickness in the literature (<xref ref-type="bibr" rid="B34">Chang et al., 2023</xref>; <xref ref-type="bibr" rid="B66">Jang et al., 2022</xref>; <xref ref-type="bibr" rid="B2">Achanccaray and Sumioka, 2023</xref>), some studies showed that spectral activity above 11&#xa0;Hz showed no significant difference (<xref ref-type="bibr" rid="B108">N&#xfc;rnberger et al., 2021</xref>) (or inconsistent trend across subjects and electrodes (<xref ref-type="bibr" rid="B109">Ozkan et al., 2023</xref>)) between baseline and severe cybersickness conditions. In our analyses, features measuring beta power were not representative of the most correlated features with cybersickness. Thus, since most of the observed beta activity was related to coupling measures, our results better align with the theory that beta is linked to the temporary cohesion of distant cortical regions (<xref ref-type="bibr" rid="B86">Li et al., 2021</xref>; <xref ref-type="bibr" rid="B152">Yang et al., 2022b</xref>), rather than due to a specific change in local activity.</p>
<p>Overall, cortical networks formed within the beta band have been associated with fundamental function of complex cognitive processes, such as active waiting and anticipation of a stimulus (<xref ref-type="bibr" rid="B22">Betti et al., 2021</xref>), temporary retention of sensory information (<xref ref-type="bibr" rid="B89">Liang et al., 2021</xref>; <xref ref-type="bibr" rid="B133">Silberstein and Klimesch, 2006</xref>), and the dynamic allocation of cognitive resources (<xref ref-type="bibr" rid="B22">Betti et al., 2021</xref>). The dynamic nature of these networks explains the rapid changes in activity observed in the beta band, thereby leading to the disparity in observations across cybersickness studies. Moreover, power change observed during high levels of cybersickness might be attributed to cybersickness related physiological states such as arousal (<xref ref-type="bibr" rid="B4">Agi&#x107; and Mandi&#x107;, 2019</xref>), cognitive effort (<xref ref-type="bibr" rid="B86">Li et al., 2021</xref>; <xref ref-type="bibr" rid="B14">Arafat et al., 2018</xref>), as well as visual and mental fatigue (<xref ref-type="bibr" rid="B48">Foong et al., 2019</xref>; <xref ref-type="bibr" rid="B156">Yue and Wang, 2019</xref>).</p>
<p>Moreover, decreases in the correlation between the beta-mtheta and beta-malpha bands at the Pz and P4 electrodes were observed as the intensity of the cybersickness symptoms increased. As shown in <xref ref-type="fig" rid="F15">Figures 14</xref>, <xref ref-type="fig" rid="F14">15</xref>, the power of the two beta-malpha and beta-mtheta bands increases with the FMS score, and their correlation decreases. These findings corroborate the importance of the AM features in capturing the temporal dynamics of the beta band.</p>
<p>According to the literature, the theta band plays a role in the temporal organization of cognitive processes (<xref ref-type="bibr" rid="B56">Herweg et al., 2016</xref>; <xref ref-type="bibr" rid="B113">Popov et al., 2018</xref>). Therefore, we hypothesize that beta-mtheta may be linked to the process of integration of sensory information mentioned earlier. Moreover, since alpha is known to reflect selective inhibition of population of neurons [as per (<xref ref-type="bibr" rid="B5">Ahn et al., 2021</xref>) and (<xref ref-type="bibr" rid="B127">Sauseng et al., 2005</xref>)], and beta is associated with intense cognitive activity [(<xref ref-type="bibr" rid="B25">Borra et al., 2023</xref>) and (<xref ref-type="bibr" rid="B54">Ghiani et al., 2021</xref>)], the beta-malpha feature may reflect a selective attention mechanism. Although alpha and beta are associated with opposite mechanisms, it is hypothesized that their interaction may serve a complementary role in the integration of extracted visual features into a coherent representation of the object (<xref ref-type="bibr" rid="B43">Di Dona and Ronconi, 2023</xref>). The proposed AM measures may be able to capturing and quantifying this interaction.</p>
</sec>
<sec id="s4-2-2">
<title>4.2.2 Alpha band insights</title>
<p>In addition to its interaction with beta, the alpha band power in the parietal cortex (channels P3, P4) was also highlighted in the analysis of the most correlated features. The increase in alpha activity in this area is indicative of sensory information processing inhibition in response to the sensory conflict induced by the VR experience. This activity appears to be a reliable marker of cybersickness, as this pattern is recurrent across EEG studies (<xref ref-type="bibr" rid="B151">Yang et al., 2022a</xref>; <xref ref-type="bibr" rid="B5">Ahn et al., 2021</xref>; <xref ref-type="bibr" rid="B78">Kim et al., 2019</xref>; <xref ref-type="bibr" rid="B1">Aboud, 2023</xref>).</p>
<p>Interestingly, the increase in alpha band identified by PSD features co-occurred with an increase in alpha-mtheta feature, suggesting that theta may play a regulatory role on inhibition similarly to what is observed with the beta band. While theta, alpha, and beta bands seem to have an intricate hierarchical role aligning with the top-down theory, the location of relevant activity in the cortex provides additional insights. In addition to revealing interactions between AM bands that suggest the coordination of distinct cognitive processes, AM features allow a better understanding of the nature of neurological processes, particularly those linked to top-down mechanisms.</p>
</sec>
<sec id="s4-2-3">
<title>4.2.3 Gamma band insights</title>
<p>The analysis the top-features obtained from the Minimal pre-processing method revealed the presence of activity in the gamma band potentially related to artifacts. <xref ref-type="fig" rid="F18">Figure 18</xref> showed that the average power in amplitude of gamma-mbeta was correlated with FMS scores, while <xref ref-type="fig" rid="F13">Figure 13</xref> showed the presence of average coupling of the gamma band with other AM bands present in <xref ref-type="table" rid="T2">Table 2</xref>. However, the presence of gamma modulated by theta and alpha in the top BCPL features presented in <xref ref-type="fig" rid="F13">Figure 13</xref> suggests rather an underlying neurological origin related to the symptom of cybersickness. Therefore, an increase in the coupling of the gamma-mtheta band would not be caused by the presence of artifacts but would serve as an additional marker of the brain&#x2019;s cognitive state during virtual reality sickness. Specifically, the fact that gamma activity is regulated by low-frequency oscillations suggests downward control mechanisms (<xref ref-type="bibr" rid="B5">Ahn et al., 2021</xref>).</p>
<p>The EEG high-frequency range, comprised of the gamma and beta bands, is thought to reflect intense local cognitive activity, as indicated by various studies (<xref ref-type="bibr" rid="B51">Freeman and Vitiello, 2015</xref>; <xref ref-type="bibr" rid="B110">Palva and Palva, 2012</xref>; <xref ref-type="bibr" rid="B71">Jerbi et al., 2010</xref>; <xref ref-type="bibr" rid="B67">Jensen and Mazaheri, 2010</xref>). These bands are often observed in the occipito-parietal region as correlated with increased cybersickness symptoms (<xref ref-type="bibr" rid="B151">Yang et al., 2022a</xref>). Given these findings, the gamma-band activity observed during the participants&#x2019; exposure to the VR simulation can be, similarly to the beta band, attributed to sensory information processing. However, both bands have separate sources and serve different roles. Gamma rhythms often involve interactions between excitatory pyramidal cells and fast-spiking inter-neurons in the formation of cell assemblies (<xref ref-type="bibr" rid="B106">Neske and Connors, 2016</xref>; <xref ref-type="bibr" rid="B107">Nunez and Srinivasan, 2010</xref>). In contrast, beta band rhythms mainly originating from gap junction-connected bursting pyramidal cells enable the binding of different neural assemblies thereby allowing a simultaneous manipulation of past and current input and the integration from different modalities (<xref ref-type="bibr" rid="B7">Alavash et al., 2017</xref>; <xref ref-type="bibr" rid="B82">Kopell et al., 2010</xref>).</p>
</sec>
<sec id="s4-2-4">
<title>4.2.4 Brain regions and lateralization insights</title>
<p>The increase in coupling variability observed in <xref ref-type="fig" rid="F12">Figure 12</xref> for the beta (CCPL_std) and beta-mtheta (AM_CCPL_std) bands was predominant in the left hemisphere (i.e., the features most correlated with the FMS score in the beta-mtheta band concern the coupling between the Pz electrode and the P3 and Cz electrodes, and in the beta band between the CP5 electrode and the P3 and P4 electrodes, as well as the coupling between P3 and Pz). The mean coupling measurement (AM_CCPL_mean and CCPL_mean), in turn, was more correlated with the FMS ratings on the right hemisphere (i.e., with P4 and CP6 electrodes).</p>
<p>In addition, the left centro-parietal region (channels CP5, P3) exhibited highly variable power in the alpha-mdelta band, thus aligning with findings from <xref ref-type="bibr" rid="B13">Angioletti and Balconi (2022)</xref>. According to the study, increased delta band activity and decreased alpha band activity in the centro-temporal cortex were indicative of a shift in attention towards endogenous sensory information. This lateralization of activity has been recognized in the literature, with right-hemisphere parietal activity associated with visuospatial attention to the environment, whereas the left hemisphere has shown to be responsible for motor coordination and planning related to proprioception (<xref ref-type="bibr" rid="B125">Rushworth et al., 2001</xref>).</p>
<p>In contrast, when processing visuo-spatial information, the superior parietal lobe and the primary visual cortex are activated (<xref ref-type="bibr" rid="B122">Rolls, 2020</xref>; <xref ref-type="bibr" rid="B88">Li et al., 2018</xref>; <xref ref-type="bibr" rid="B11">Andersson et al., 2019</xref>), which have nearest electrodes Cz, Pz, P3, Pz, and P4. Consistent with these studies, we posit that the coupling variability is associated with active cognitive processes in this area, particularly those involving proprioceptive information rather than visual information. This implies that shifts of attention towards proprioceptive information may either instigate or respond to cybersickness. This hemispheric phenomenon during cybersickness was well captured by the new AM features.</p>
<p>In addition to the lateralized role, the study in <xref ref-type="bibr" rid="B91">Limanowski and Friston (2020)</xref> also revealed significant bilateral activity in the superior parietal lobe&#x2013;covered by electrodes Pz and Cz&#x2013;where its role would be to resolve inter-sensory conflict, enabling the maintenance of a unique body representation. Therefore, this region plays an important role in the management of the cognitive processes that process sensory information.</p>
<p>Interestingly, within Cz, an increasing alpha-mdelta power observed in <xref ref-type="fig" rid="F9">Figure 9</xref> was accompanied by an increase in its coupling with the beta-mdelta and beta-mbeta features over Cz and Fz observed in <xref ref-type="fig" rid="F13">Figure 13</xref>. This coupling was shown with the mutual information measurement analysis, thus suggesting a nonlinear relationship between alpha and beta band activity.</p>
<p>Moreover, <xref ref-type="fig" rid="F13">Figure 13</xref> showed that the delta band frequently appears to modulate the amplitude of both the alpha and beta bands, thereby controlling their activity. This observation supports the top-down control theory, which suggests long-distance control from the brain&#x2019;s decision-making centers to local cortical activity.</p>
</sec>
</sec>
<sec id="s4-3">
<title>4.3 Limitations and future work</title>
<p>This research presents some limitations. First, the use of a non-linear SVR kernel made it difficult to analyze feature ranking by inherent regularization, which is possible only with linear kernels. As a result, we relied on Spearman correlation for feature ranking, which does not consider the interaction between features. Future work may explore the use of more advanced feature selection methods that take such interactions into account, such as the mRMR (Minimum Redundancy Maximum Relevance) (<xref ref-type="bibr" rid="B44">Ding and Peng, 2005</xref>).</p>
<p>The findings of this study apply primarily to open-loop VR systems, where users have limited control over motion stimuli. EEG patterns observed under these conditions may not directly translate to closed-loop systems, where active control relies on anticipatory mechanisms, as shown in research comparing drivers and passengers (<xref ref-type="bibr" rid="B45">Dong et al., 2011</xref>; <xref ref-type="bibr" rid="B123">Rolnick and Lubow, 1991</xref>), in contrast to the compensatory responses observed in open-loop scenarios. While the study provides valuable insights into the neural correlates of cybersickness, its findings are primarily applicable to open-loop VR systems. Given that closed-loop systems are more common among general VR users, further research is needed to validate the relevance of these markers in user-controlled environments.</p>
<p>Moreover, here we relied on the efficiency metrics for pre-processing algorithms based on the mutual information difference with head accelerometer and one EOG time serie. Other artifacts may contaminate the EEG signals, such as muscle movements, poor electrode-skin contact, and sweat, to name few. Continuous measurement of such signals are more challenging, but alternate modalities, such as galvanic skin response, facial electromyography (EMG), or impedance measurements may provide additional cues for future works. Emerging VR headsets are already including such modalities directly into the head-mounted display, thus facilitating this type of analyses in the future. In this study, we relied on a publicly available dataset, which primarily included artifacts from ocular and head movements. While these are common in VR scenarios, future work should validate the impact of minimal preprocessing under a broader range of artifact types to ensure the generalizability of these findings.</p>
<p>Lastly, the proposed work relied on publicly available data, which was collected from a limited number of participants, and not all of them completed the full task. This limitation led to variability across subjects, particularly at higher FMS rating levels. Additionally, the dataset&#x2019;s gender composition (31 females, 9 males) introduces a potential bias, as the findings may predominantly reflect female responses, consistent with studies reporting higher susceptibility to motion sickness among females (<xref ref-type="bibr" rid="B83">Koslucher et al., 2015</xref>; <xref ref-type="bibr" rid="B103">Munafo et al., 2017</xref>). Furthermore, while this study focused on the sensory conflict theory, other theories, such as the ecological theory of motion sickness and postural instability (<xref ref-type="bibr" rid="B135">Stanney et al., 2020</xref>; <xref ref-type="bibr" rid="B117">Riccio and Stoffregen, 1991</xref>), emphasize individual differences and environmental interactions that were beyond the scope of this work. Future research could investigate these complementary perspectives and employ advanced cross-subject generalization tools (e.g. (<xref ref-type="bibr" rid="B9">Albuquerque et al., 2022</xref>)) to address these limitations.</p>
</sec>
</sec>
<sec sec-type="conclusion" id="s5">
<title>5 Conclusion</title>
<p>In this study, we sought to answer two main research questions: (1) what role does EEG pre-processing play on overall cybersickness characterization?, and (2) what neural patterns can be indicative of cybersickness levels? To help answer these questions, we processed a publicly-available EEG-cybersickness dataset with three pre-processing methods, from minimal to more complex methods removing head and eye movements, as well as explored several benchmark power spectral and coupling features. To assist with question &#x23;2, we also explored new amplitude modulation power and coupling measures to capture interactivity between frequency bands and channels. We showed that, indeed, minimal processing kept head and eye movement related cues that were important for cybersickness detection, but did not provide a full glimpse into the neural patterns associated with cybersickness. To this end, a more complex pre-processing method was used. Ultimately, several AM and coupling measures showed to be top-performing features, thus emphasizing their complementarity to PSD parameters and their importance for cybersickness prediction.</p>
</sec>
</body>
<back>
<sec sec-type="data-availability" id="s6">
<title>Data availability statement</title>
<p>Publicly available datasets were analyzed in this study. This data can be found here: <ext-link ext-link-type="uri" xlink:href="https://zenodo.org/records/6373681">https://zenodo.org/records/6373681</ext-link>.</p>
</sec>
<sec sec-type="ethics-statement" id="s7">
<title>Ethics statement</title>
<p>The studies involving humans were approved by the University of Glasgow (No. 300200009), College of Science and Engineering. The studies were conducted in accordance with the local legislation and institutional requirements. Written informed consent for participation was not required from the participants or the participants&#x2019; legal guardians/next of kin in accordance with the national legislation and institutional requirements.</p>
</sec>
<sec sec-type="author-contributions" id="s8">
<title>Author contributions</title>
<p>OR: Formal Analysis, Investigation, Software, Writing&#x2013;original draft, Writing&#x2013;review and editing. DB: Conceptualization, Methodology, Resources, Writing&#x2013;original draft, Writing&#x2013;review and editing. GK: Conceptualization, Resources, Writing&#x2013;original draft, Writing&#x2013;review and editing. SP: Conceptualization, Methodology, Resources, Writing&#x2013;original draft, Writing&#x2013;review and editing. NB: Writing&#x2013;original draft, Writing&#x2013;review and editing. TF: Conceptualization, Methodology, Resources, Supervision, Writing&#x2013;original draft, Writing&#x2013;review and editing.</p>
</sec>
<sec sec-type="funding-information" id="s9">
<title>Funding</title>
<p>The author(s) declare that financial support was received for the research, authorship, and/or publication of this article. The authors would like to acknowledge funding from the Natural Sciences and Engineering Research Council of Canada, MITACS, and Thales Digital Solutions Inc. under the Alliance Grants Program (ALLRP576732 - 22).</p>
</sec>
<ack>
<p>ChatGPT-4 and Copilot were used in drafting of the very first version of the introductory text. The generated text was then fully reviewed and edited by the author(s), who take full responsibility for the final content presented here.</p>
</ack>
<sec sec-type="COI-statement" id="s10">
<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 sec-type="disclaimer" id="s11">
<title>Publisher&#x2019;s note</title>
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<sec id="s12">
<title>Glossary</title>
<def-list>
<def-item>
<term id="G1-frvir.2025.1468971">
<bold>AAR</bold>
</term>
<def>
<p>Automatic Artifact Removal</p>
</def>
</def-item>
<def-item>
<term id="G2-frvir.2025.1468971">
<bold>AM</bold>
</term>
<def>
<p>Amplitude Modulation</p>
</def>
</def-item>
<def-item>
<term id="G3-frvir.2025.1468971">
<bold>AM-BCPL</bold>
</term>
<def>
<p>Amplitude Modulation inter-band coupling</p>
</def>
</def-item>
<def-item>
<term id="G4-frvir.2025.1468971">
<bold>AM-CCPL</bold>
</term>
<def>
<p>Amplitude Modulation inter-channel coupling</p>
</def>
</def-item>
<def-item>
<term id="G5-frvir.2025.1468971">
<bold>AMP</bold>
</term>
<def>
<p>Amplitude Modulation Power</p>
</def>
</def-item>
<def-item>
<term id="G6-frvir.2025.1468971">
<bold>ASR</bold>
</term>
<def>
<p>artifact Subspace Reconstruction</p>
</def>
</def-item>
<def-item>
<term id="G7-frvir.2025.1468971">
<bold>BCPL</bold>
</term>
<def>
<p>Inter-band coupling</p>
</def>
</def-item>
<def-item>
<term id="G8-frvir.2025.1468971">
<bold>BFT</bold>
</term>
<def>
<p>Band-filtered time series</p>
</def>
</def-item>
<def-item>
<term id="G9-frvir.2025.1468971">
<bold>CCPL</bold>
</term>
<def>
<p>Inter-channel coupling</p>
</def>
</def-item>
<def-item>
<term id="G10-frvir.2025.1468971">
<bold>EOG</bold>
</term>
<def>
<p>Electrooculography</p>
</def>
</def-item>
<def-item>
<term id="G11-frvir.2025.1468971">
<bold>FIR</bold>
</term>
<def>
<p>Finite impulse response</p>
</def>
</def-item>
<def-item>
<term id="G12-frvir.2025.1468971">
<bold>FMS</bold>
</term>
<def>
<p>Fast Motion Sickness</p>
</def>
</def-item>
<def-item>
<term id="G13-frvir.2025.1468971">
<bold>ICA</bold>
</term>
<def>
<p>Independent Component Analysis</p>
</def>
</def-item>
<def-item>
<term id="G14-frvir.2025.1468971">
<bold>PSD</bold>
</term>
<def>
<p>Power Spectral Density</p>
</def>
</def-item>
<def-item>
<term id="G15-frvir.2025.1468971">
<bold>SNR</bold>
</term>
<def>
<p>Signal-to-Noise Ratio</p>
</def>
</def-item>
<def-item>
<term id="G16-frvir.2025.1468971">
<bold>SSQ</bold>
</term>
<def>
<p>Simulator Sickness Questionnaire</p>
</def>
</def-item>
<def-item>
<term id="G17-frvir.2025.1468971">
<bold>SVR</bold>
</term>
<def>
<p>Support Vector Regressor</p>
</def>
</def-item>
<def-item>
<term id="G18-frvir.2025.1468971">
<bold>VR</bold>
</term>
<def>
<p>Virtual Reality</p>
</def>
</def-item>
</def-list>
</sec>
</back>
</article>