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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Pharmacol.</journal-id>
<journal-title>Frontiers in Pharmacology</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Pharmacol.</abbrev-journal-title>
<issn pub-type="epub">1663-9812</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">1194672</article-id>
<article-id pub-id-type="doi">10.3389/fphar.2023.1194672</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Pharmacology</subject>
<subj-group>
<subject>Original Research</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Validation of the Arabic version of the general medication adherence scale in patients with type 2 diabetes mellitus in Jordan</article-title>
<alt-title alt-title-type="left-running-head">Islam 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/fphar.2023.1194672">10.3389/fphar.2023.1194672</ext-link>
</alt-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Islam</surname>
<given-names>Md. Ashraful</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="corresp" rid="c001">&#x2a;</xref>
<uri xlink:href="https://loop.frontiersin.org/people/847897/overview"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>El-Dahiyat</surname>
<given-names>Faris</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/715719/overview"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Nouri</surname>
<given-names>Ahmed</given-names>
</name>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/503595/overview"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Alefan</surname>
<given-names>Qais</given-names>
</name>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/2260884/overview"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Naqvi</surname>
<given-names>Atta Abbas</given-names>
</name>
<xref ref-type="aff" rid="aff5">
<sup>5</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1996303/overview"/>
</contrib>
</contrib-group>
<aff id="aff1">
<sup>1</sup>
<institution>Department of Pharmacy Practice</institution>, <institution>College of Clinical Pharmacy</institution>, <institution>Imam Abdulrahman Bin Faisal University</institution>, <addr-line>Dammam</addr-line>, <country>Saudi Arabia</country>
</aff>
<aff id="aff2">
<sup>2</sup>
<institution>Clinical Pharmacy Program</institution>, <institution>College of Pharmacy</institution>, <institution>Al Ain University</institution>, <addr-line>Al Ain</addr-line>, <country>United Arab Emirates</country>
</aff>
<aff id="aff3">
<sup>3</sup>
<institution>Medical Faculty</institution>, <institution>Institute of Anatomy II</institution>, <institution>University Hospital D&#xfc;sseldorf</institution>, <institution>Heinrich-Heine-University</institution>, <addr-line>D&#xfc;sseldorf</addr-line>, <country>Germany</country>
</aff>
<aff id="aff4">
<sup>4</sup>
<institution>Department of Clinical Pharmacy</institution>, <institution>Faculty of Pharmacy</institution>, <institution>Jordan University of Science and Technology</institution>, <addr-line>Irbid</addr-line>, <country>Jordan</country>
</aff>
<aff id="aff5">
<sup>5</sup>
<institution>Department of Pharmacy Practice</institution>, <institution>School of Pharmacy</institution>, <institution>University of Reading</institution>, <institution>Whiteknights Campus</institution>, <addr-line>Reading</addr-line>, <country>United Kingdom</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/1995901/overview">Andr&#xe9; Coelho</ext-link>, Instituto Polit&#xe9;cnico de Lisboa, Portugal</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/510752/overview">Nadeem Irfan Bukhari</ext-link>, University of the Punjab, Pakistan</p>
<p>
<ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/2365545/overview">Teresa Guimar&#xe3;es</ext-link>, Instituto Polit&#xe9;cnico de Lisboa, Portugal</p>
<p>
<ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/1045058/overview">Ana Margarida Costa-Veiga</ext-link>, Instituto Polit&#xe9;cnico de Lisboa, Portugal</p>
</fn>
<corresp id="c001">&#x2a;Correspondence: Md. Ashraful Islam, <email>salimashraf.ru@gmail.com</email>
</corresp>
</author-notes>
<pub-date pub-type="epub">
<day>20</day>
<month>09</month>
<year>2023</year>
</pub-date>
<pub-date pub-type="collection">
<year>2023</year>
</pub-date>
<volume>14</volume>
<elocation-id>1194672</elocation-id>
<history>
<date date-type="received">
<day>27</day>
<month>03</month>
<year>2023</year>
</date>
<date date-type="accepted">
<day>04</day>
<month>09</month>
<year>2023</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#xa9; 2023 Islam, El-Dahiyat, Nouri, Alefan and Naqvi.</copyright-statement>
<copyright-year>2023</copyright-year>
<copyright-holder>Islam, El-Dahiyat, Nouri, Alefan and Naqvi</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>
<bold>Background:</bold> Medication adherence is a major challenge for patients with diabetes. Adherence rates are often low, and this can lead to poor glycaemic control and increased risk of complications. There are a number of tools available to measure medication adherence, but few have been validated in Arabic-speaking populations.</p>
<p>
<bold>Aim:</bold> This study aimed to validate the Arabic version of the General Medication Adherence Scale in patients with type 2 diabetes in Jordan.</p>
<p>
<bold>Methods:</bold> A cross-sectional study was conducted for 3&#xa0;months among patients attending diabetes mellitus outpatient clinic in Irbid, Jordan. The validation procedure included confirmatory factor analysis (CFA) and equation modelling (SEM). Fit indices, namely, goodness of fit index (GFI), Tucker Lewis index (TLI), comparative fit index (CFI), and root mean square error of approximation (RMSEA) were observed. Corrected item-total correlation (ITC) was reported. Reliability was assessed using Cronbach&#x2019;s alpha (&#x3b1;) and &#x3b1; value based on item deletion was also carried out. Intraclass correlation coefficient (ICC) was reported. Data were analyzed using IBM SPSS v23 and IBM AMOS v25.</p>
<p>
<bold>Results:</bold> Data from 119 participants were gathered. The mean adherence score was 27.5 (&#xb1;6) ranging from 6 to 33. More than half of the patients were adherent to their therapy (n &#x3d; 79, 66.4%). The reliability of the scale (n &#x3d; 11) was 0.907, and ICC ranged from 0.880&#x2014;0.930: 95% CI. The following values were observed in CFA; &#x3c7;<sup>2</sup> &#x3d; 62.158, df &#x3d; 41, &#x3c7;<sup>2</sup>/df &#x3d; 1.516, GFI &#x3d; 0.913, AGFI &#x3d; 0.860, TLI &#x3d; 0.960, CFI &#x3d; 0.971 and RMSEA &#x3d; 0.066. A total of 10 out of 11 items had corrected ITC &#x3e;0.5. The &#x3b1; remained between 0.89&#x2013;0.92 during item deletion.</p>
<p>
<bold>Conclusion:</bold> The results obtained in this study suggest that the scale is valid and reliable in measuring adherence to medications in the studied sample of patients with diabetes. This scale can be used by clinicians in Jordan to assess adherence and may further aide in evaluating interventions to improve adherence rates in persons with type 2 diabetes.</p>
</abstract>
<kwd-group>
<kwd>validation studies</kwd>
<kwd>patient compliance</kwd>
<kwd>medication adherence</kwd>
<kwd>diabetes</kwd>
<kwd>Jordan</kwd>
</kwd-group>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-at-acceptance</meta-name>
<meta-value>Drugs Outcomes Research and Policies</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<sec id="s1">
<title>1 Introduction</title>
<p>Chronic illnesses are usually prolonged illnesses that are managed throughout the course of a patient&#x2019;s life and are not often completely cured (<xref ref-type="bibr" rid="B9">Dowrick et al., 2005</xref>). They may require either life-long or long-term medication therapy and the success of long-term treatments depends on proper adherence to the medication therapy regimen (<xref ref-type="bibr" rid="B25">World Health Organization, 2003</xref>; <xref ref-type="bibr" rid="B9">Dowrick et al., 2005</xref>; <xref ref-type="bibr" rid="B19">Naqvi et al., 2019</xref>). According to the Institute for Health Metrics and Evaluation (IHME), chronic illnesses remain the leading cause of death alone, as well as death and disability combined. Seven chronic diseases are listed among the top 10 causes of death among the Jordanian population (<xref ref-type="bibr" rid="B12">Institute of Health Metrics and Evaluation IHME, 2020</xref>).</p>
<p>One of the most common reasons for failing to achieve treatment outcomes by patients with chronic illnesses is non-adherence to medication therapy (<xref ref-type="bibr" rid="B21">Naqvi et al., 2020a</xref>). The World Health Organization (WHO) defines adherence as the as the degree to which a person&#x2019;s medicine taking behaviour, lifestyle changes, and dietary habits align with the recommendations given by a healthcare professional (<xref ref-type="bibr" rid="B26">World Health Organization, 2003</xref>). Non-adherence to pharmacotherapy may result in disease complications, prolonged disease condition, increased risk for hospitalization, risk of disability and death; all of these may further exacerbate the healthcare costs (<xref ref-type="bibr" rid="B21">Naqvi et al., 2020a</xref>; <xref ref-type="bibr" rid="B1">Al-Qasem et al., 2011</xref>; <xref ref-type="bibr" rid="B14">Iuga and McGuire, 2014</xref>). Non-adherence continues to prevail in developing countries as evidence highlights that only 50% of patients with chronic illnesses adhere to the treatment (<xref ref-type="bibr" rid="B26">World Health Organization, 2003</xref>). A review by Al-Qasem et al. highlighted that the practice of non-adherence was prevalent among patients in the Middle Eastern countries. The rate of non-adherence to medications was reported to be between 1.4% and 88% (<xref ref-type="bibr" rid="B1">Al-Qasem et al., 2011</xref>).</p>
<p>In Jordan, medication non-adherence is a serious healthcare issue where most patients are non-adherent (<xref ref-type="bibr" rid="B4">Al-Sahouri et al., 2019</xref>). For example, in a study that evaluated the effectiveness of home medication management review on medication adherence in Jordanian patients, most patients had medium adherence at baseline (<xref ref-type="bibr" rid="B6">Al&#x2010;Qudah et al., 2018</xref>). Moreover, in another study among patients with chronic ailments in Jordan, it was reported that 46.1% were non-adherent (<xref ref-type="bibr" rid="B8">Basheti et al., 2016</xref>). Focusing on type 2 diabetes (T2DM), it was reported that slightly less than half of the surveyed T2DM patients (46.5%) had moderate adherence while 12.2% had low adherence to their anti-diabetic medications (<xref ref-type="bibr" rid="B3">Al-Qerem et al., 2021</xref>).</p>
<p>In the past, adherence to medication among patients in Jordan has been documented using the Arabic versions of the 8&#x2013;item Morisky&#x2019;s Medication Adherence Scale (MMAS&#x2014;8), Beliefs about Medication Questionnaire (BMQ), and Medication Adherence Report Scale (MARS) (<xref ref-type="bibr" rid="B7">Awwad et al., 2015</xref>; <xref ref-type="bibr" rid="B8">Basheti et al., 2016</xref>; <xref ref-type="bibr" rid="B5">Alsous et al., 2017</xref>; <xref ref-type="bibr" rid="B6">Al&#x2010;Qudah et al., 2018</xref>; <xref ref-type="bibr" rid="B3">Al-Qerem et al., 2021</xref>; <xref ref-type="bibr" rid="B2">Al-Qerem et al., 2022</xref>). Recently, the Arabic version of the General Medication Adherence Scale (GMAS) was validated in patients with chronic diseases in Saudi Arabia and in patients with diabetes in Sudan and Morocco (<xref ref-type="bibr" rid="B1">Al-Qasem et al., 2011</xref>; <xref ref-type="bibr" rid="B15">Mahmoud et al., 2021</xref>; <xref ref-type="bibr" rid="B16">Maryem et al., 2023</xref>). This scale considers non-adherence due to the cost of medications which adds a financial aspect in reporting medication adherence. The concurrent validity of the Arabic version has been evaluated by correlating the adherence scores obtained by GMAS&#x2014;AR with the ones obtained by the Arabic versions of Adherence to Refills and Medications Scale (ARMS) and MARS in Saudi Arabia (<xref ref-type="bibr" rid="B13">Islam et al., 2021</xref>). Thus, validation of this scale is a prerequisite to enable clinicians to use the scale in Jordan.</p>
</sec>
<sec id="s2">
<title>2 Objective</title>
<p>The aim of this study was to validate the Arabic version of the General Medication Adherence Scale (GMAS&#x2014;AR) in Jordanian patients with type 2 diabetes mellitus (T2DM).</p>
</sec>
<sec sec-type="methods" id="s3">
<title>3 Methods</title>
<sec id="s3-1">
<title>3.1 Study design</title>
<p>A cross-sectional study was conducted from August to October 2018 in an outpatient department at King Abdullah University Hospital (KAUH) in Irbid, Jordan.</p>
</sec>
<sec id="s3-2">
<title>3.2 Participants</title>
<p>The target population for this study was persons with type 2 diabetes. All adult males and females who were diagnosed with T2DM at least 3&#xa0;months before the study, were invited. Further eligibility criteria included being prescribed medications for diabetes, with or without comorbidity, and in the implementation stage. The implementation stage of medication adherence is the stage where an individual has started taking medications as prescribed (<xref ref-type="bibr" rid="B25">Vrijens et al., 2012</xref>; <xref ref-type="bibr" rid="B23">Ribaut et al., 2020</xref>). Besides, patients who were admitted to a hospital, had acute illnesses, were pregnant or had planned pregnancy, were breastfeeding, and so on, were not eligible. Moreover, those who did not consent to participate were excluded.</p>
</sec>
<sec id="s3-3">
<title>3.3 Sample size</title>
<p>The suggested sample size for factor analysis ranges from 3&#x2014;20&#xa0;times the number of variables, while the absolute sample size ranges from 100&#x2014;1000 (<xref ref-type="bibr" rid="B17">Mundfrom et al., 2005</xref>). A convenience sampling method was employed to select 100&#x2013;150 participants. This was based on the findings of Muth&#xe9;n and Muth&#xe9;n that confirmatory factor analysis (CFA) with normally distributed and no missing data may yield a power of 0.8 (<xref ref-type="bibr" rid="B18">Muth&#xe9;n and Muth&#xe9;n, 2002</xref>).</p>
</sec>
<sec id="s3-4">
<title>3.4 Research instrument</title>
<p>The Arabic version of the General Medication Adherence Scale (GMAS) was used with permission (<xref ref-type="bibr" rid="B21">Naqvi et al., 2020a</xref>). The scale consisted of 11 items that measured adherence to medications. Each item had 4 possible responses, and each response had a score. Participants were asked to select the item that best described their medicine-taking practice. The scores from all individual items were summed up to report a cumulative adherence score. The maximum achievable adherence score was 33, and was categorized into categories; poor (0&#x2014;10), low (11&#x2014;16), partial (17&#x2014;26), good (27&#x2014;29), and high (30&#x2014;33) adherence (<xref ref-type="bibr" rid="B21">Naqvi et al., 2020a</xref>). Additionally, the score could be categorized as dichotomous, i.e., adherent (&#x2265;27) and non-adherent (&#x2264;26). The detailed scoring of the scale is described previously (<xref ref-type="bibr" rid="B20">Naqvi et al., 2020a</xref>; <xref ref-type="bibr" rid="B20">Naqvi et al., 2020b</xref>).</p>
</sec>
<sec id="s3-5">
<title>3.5 Statistical analysis</title>
<p>The model fitness was evaluated by confirmatory factor analysis (CFA). It was conducted with the formation of a structural equation model for a three-factor model. The 3-factor model was considered based on the previous validation of the Arabic version among patients in Sudan and Saudi Arabia (<xref ref-type="bibr" rid="B20">Naqvi et al., 2020a</xref>; <xref ref-type="bibr" rid="B15">Mahmoud et al., 2021</xref>). Fit indices, namely, goodness of fit index (GFI), Tucker Lewis index (TLI), comparative fit index (CFI), and root mean square error of approximation (RMSEA) were observed. The factor validity was established if the fit indices were in the acceptable range, i.e., GFI, AGFI, TLI, CFI &#x3e;0.9, and RMSEA &#x3c;0.08.</p>
<p>In addition, the construct validity was assessed. measured by assessing the corrected item-total correlation. This assessment was carried out by adopting the methods used by Raharjanti and others to assess construct validity (<xref ref-type="bibr" rid="B22">Raharjanti et al., 2022</xref>). Construct validity is the extent to which an assessment measures a theoretical concept it is expected to measure (<xref ref-type="bibr" rid="B10">Hajjar, 2018</xref>). The item total correlation (ITC) was analysed. An ITC between 0.3 and 0.49 was considered moderate while ITC &#x3e;0.5 was considered strong (<xref ref-type="bibr" rid="B10">Hajjar, 2018</xref>).</p>
<p>Further, the reliability was assessed using Cronbach&#x2019;s alpha and was considered satisfactory if it was &#x3e;0.7 (<xref ref-type="bibr" rid="B24">Sarmento and Costa, 2019</xref>). Also, item-deletion was carried out to review the contribution of each item towards internal consistency of scale.</p>
</sec>
<sec id="s3-6">
<title>3.6 Data collection and reporting</title>
<p>An informed written consent form was sought from participants before handing the survey. Participants who returned signed consent forms were provided with the questionnaire. Participants were informed that participation was voluntary, and their decision to participate will not have any impact on the healthcare they receive. The questionnaire had no personal identifiers and were stored separately to the consent forms. The data was collected once from a participant at the venue. Patients who were eligible at the hospital were approached for recruitment. The questionnaire was handed to the participant for self-administration and was collected later. It was without any personal identifiers, and hence, it could not be linked to the participants.</p>
<p>The data initially gathered was coded in Microsoft Excel. Later, it was imported and analysed using IBM SPSS version 23 (Armonk, NY). CFA was conducted using IBM AMOS version 25. The data was digitized and verified. Categorical data were expressed in sample count (n) and percentage (%), while continuous data were expressed in mean (X) and standard deviation (SD).</p>
</sec>
<sec id="s3-7">
<title>3.7 Ethics statement and informed consent</title>
<p>The study was approved by the Institutional Review Board of Jordan University of Science and Technology (Ref: 59/117/2018). Participants were informed that the study participation was voluntary and their decision to participate would not have any impact on the healthcare they receive. The questionnaires had no personal identifiers and were stored separately to the consent forms.</p>
</sec>
</sec>
<sec sec-type="results" id="s4">
<title>4 Results</title>
<p>A total of 119 completed and useable surveys were received.</p>
<sec id="s4-1">
<title>4.1 Participants&#x2019; characteristics</title>
<p>The mean age of participants was 56.4 (&#xb1;15.07) years. Most participants were above 50&#xa0;years (n &#x3d; 80, 67.2%), identified as female (n &#x3d; 70, 58.8%), and indicated their status as married (n &#x3d; 89, 74.8%). Most participants were graduates (n &#x3d; 47, 39.5%) and had a monthly income between JOD 201&#x2014;500 (n &#x3d; 41, 34.5%). Majority of participants were prescribed up to 2 medications (n &#x3d; 108, 90.2%), had comorbidities (n &#x3d; 65, 54.6%), and received medicines by government supply (n &#x3d; 57, 47.9%).</p>
<p>The mean Hb<sub>A1c</sub> was 7.65 (&#xb1;1.34) % (95% CI, 7.41%&#x2014;7.9%). The mean random blood glucose was reported at 185.4 (&#xb1;71.5) mg/dL (95% CI: 172.5&#xa0;mg/dL&#x2014;198.5&#xa0;mg/dL). Of those (n &#x3d; 65, 54.6%) who indicated having comorbidities, 40 patients had single comorbidity, i.e., hypertension (HTN), asthma (n &#x3d; 1), gout (n &#x3d; 1), kidney disease (n &#x3d; 1), irritable bowel syndrome (n &#x3d; 1), ulcer (n &#x3d; 1), dyslipidaemia (n &#x3d; 1), thyroid disease (n &#x3d; 1), previous heart failure (HF) (n &#x3d; 1), and neck and back pain (n &#x3d; 2). Fifteen patients had multimorbidity, i.e., HTN and arthritis (n &#x3d; 1), HTN and kidney disease (n &#x3d; 1), gout and arthritis (n &#x3d; 1), HTN and prostate enlargement (n &#x3d; 1), dyslipidaemia and previous HF (n &#x3d; 1), HTN and osteoporosis (n &#x3d; 1), asthma and arthritis (n &#x3d; 1), HTN and dyslipidaemia (n &#x3d; 3), HTN and a previous case of heart failure (HF) (n &#x3d; 3), HTN, asthma and rheumatoid arthritis (RA) (n &#x3d; 1), HTN, gout and dyslipidaemia (n &#x3d; 1). The mean adherence score was 27.5 (&#xb1;6) and ranged from 6 to 33. About two-third of the sample were adherent to their therapy (n &#x3d; 79, 66.4%) (<xref ref-type="table" rid="T1">Table 1</xref>).</p>
<table-wrap id="T1" position="float">
<label>TABLE 1</label>
<caption>
<p>Sociodemographic and adherence characteristics of participants (n &#x3d; 119).</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="left">Characteristics</th>
<th align="left">Frequency (n)</th>
<th align="left">Percentage (%)</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td colspan="3" align="left">
<bold>Age</bold>
</td>
</tr>
<tr>
<td align="left">&#x2264;50 years</td>
<td align="center">39</td>
<td align="center">32.8</td>
</tr>
<tr>
<td align="left">&#x3e;50 years</td>
<td align="center">80</td>
<td align="center">67.2</td>
</tr>
<tr>
<td colspan="3" align="left">
<bold>Gender</bold>
</td>
</tr>
<tr>
<td align="left">Male</td>
<td align="center">49</td>
<td align="center">41.2</td>
</tr>
<tr>
<td align="left">Female</td>
<td align="center">70</td>
<td align="center">58.8</td>
</tr>
<tr>
<td colspan="3" align="left">
<bold>Marital status</bold>
</td>
</tr>
<tr>
<td align="left">Single</td>
<td align="center">12</td>
<td align="center">10.1</td>
</tr>
<tr>
<td align="left">Married</td>
<td align="center">89</td>
<td align="center">74.8</td>
</tr>
<tr>
<td align="left">Other</td>
<td align="center">18</td>
<td align="center">15.1</td>
</tr>
<tr>
<td colspan="3" align="left">
<bold>Education</bold>
</td>
</tr>
<tr>
<td align="left">Primary</td>
<td align="center">25</td>
<td align="center">21</td>
</tr>
<tr>
<td align="left">Secondary</td>
<td align="center">21</td>
<td align="center">17.6</td>
</tr>
<tr>
<td align="left">Intermediate</td>
<td align="center">26</td>
<td align="center">21.8</td>
</tr>
<tr>
<td align="left">Graduate</td>
<td align="center">47</td>
<td align="center">39.5</td>
</tr>
<tr>
<td colspan="3" align="left">
<bold>Monthly income (USD)&#x2a;</bold>
</td>
</tr>
<tr>
<td align="left">JOD &#x2264;200 (USD &#x2264;282.09)</td>
<td align="center">24</td>
<td align="center">20.2</td>
</tr>
<tr>
<td align="left">JOD 201&#x2014;500 (USD 283.5&#x2013;705.23)</td>
<td align="center">41</td>
<td align="center">34.5</td>
</tr>
<tr>
<td align="left">JOD 501&#x2014;700 (USD 706.64&#x2013;987.32)</td>
<td align="center">30</td>
<td align="center">25.2</td>
</tr>
<tr>
<td align="left">JOD 701&#x2014;1000 (USD 988.73&#x2013;1410.45)</td>
<td align="center">13</td>
<td align="center">10.9</td>
</tr>
<tr>
<td align="left">JOD &#x3e;1000 (USD &#x3e;1410.45)</td>
<td align="center">11</td>
<td align="center">9.2</td>
</tr>
<tr>
<td colspan="3" align="left">
<bold>Comorbidities</bold>
</td>
</tr>
<tr>
<td align="left">Yes</td>
<td align="center">65</td>
<td align="center">54.6</td>
</tr>
<tr>
<td align="left">No</td>
<td align="center">54</td>
<td align="center">45.4</td>
</tr>
<tr>
<td colspan="3" align="left">
<bold>Number of Medicine taken</bold>
</td>
</tr>
<tr>
<td align="left">&#x2264;2</td>
<td align="center">108</td>
<td align="center">90.8</td>
</tr>
<tr>
<td align="left">&#x3e;2</td>
<td align="center">11</td>
<td align="center">9.2</td>
</tr>
<tr>
<td colspan="3" align="left">
<bold>Mode of obtaining most medicines</bold>
</td>
</tr>
<tr>
<td align="left">Government supply</td>
<td align="center">57</td>
<td align="center">47.9</td>
</tr>
<tr>
<td align="left">Insurance</td>
<td align="center">23</td>
<td align="center">19.3</td>
</tr>
<tr>
<td align="left">Out of pocket</td>
<td align="center">39</td>
<td align="center">32.8</td>
</tr>
<tr>
<td colspan="3" align="left">
<bold>Adherence status</bold>
</td>
</tr>
<tr>
<td align="left">Non-adherent to therapy</td>
<td align="center">40</td>
<td align="center">33.6</td>
</tr>
<tr>
<td align="left">Adherent to therapy</td>
<td align="center">79</td>
<td align="center">66.4</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>&#x2a;1 Jordanian Dinar (JOD) equals United States Dollar (USD) 1.41&#xa0;at the time of this writing.</p>
</fn>
</table-wrap-foot>
</table-wrap>
</sec>
<sec id="s4-2">
<title>4.2 Validation results of GMAS-AR</title>
<sec id="s4-2-1">
<title>4.2.1 Model fitness using confirmatory factor analysis</title>
<p>The <xref ref-type="fig" rid="F1">Figure 1</xref> shows the results of a confirmatory factor analysis (CFA) of GMAS. The CFA results showed that a 3-factor model of the GMAS had a good fit to the data, with all of the fit indices within acceptable ranges. The three factors were: Factor 1: Behaviour related non-adherence, Factor 2: Comorbidity and medication related non-adherence, Factor 3: Cost-related non-adherence. The factor loadings for the 3-factor model were all significant, with most of the loadings being in the moderate to strong range. This suggests that the 3-factor model is a good representation of the underlying structure of the GMAS. CFA analysis together with SEM modelling for a 3&#x2014;factor structure showed a model fit with fit indices in acceptable ranges. The values were as follows: &#x3c7;<sup>2</sup> &#x3d; 62.158, df &#x3d; 41, <italic>p</italic> &#x3d; 0.018, &#x3c7;<sup>2</sup>/df &#x3d; 1.516, GFI &#x3d; 0.913, AGFI &#x3d; 0.860, TLI &#x3d; 0.960, CFI &#x3d; 0.971 and RMSEA &#x3d; 0.066.</p>
<fig id="F1" position="float">
<label>FIGURE 1</label>
<caption>
<p>Structural equation model.</p>
</caption>
<graphic xlink:href="fphar-14-1194672-g001.tif"/>
</fig>
</sec>
<sec id="s4-2-2">
<title>4.2.2 Construct validity</title>
<p>The corrected ITC values for each item of the questionnaire were analysed. The highest value for corrected item-total correlation ITC was 0.807 while the lowest value was 0.275.10 out of 11 items had corrected ITC values &#x3e;0.5 indicating a strong contribution towards overall medication adherence. All values were positive (&#x2b;). One item (item 11) had a corrected ITC value of 0.275 which was &#x3c;0.3. Item 11 of the questionnaire assessed cost-related non-adherence, a distinct facet of adherence that is differentiated from patient behaviours, comorbidities, and pill burden. Therefore, it was retained. The scale was considered to have construct validity.</p>
</sec>
</sec>
<sec id="s4-3">
<title>4.3 Reliability results of GMAS-AR</title>
<p>The overall reliability (Cronbach&#x2019;s &#x3b1;) of the scale (n &#x3d; 11) was 0.907. The intraclass correlation coefficient was reported at 0.907 (95% CI, 0.880&#x2014;0.930). The reliability of the scale remained between 0.89&#x2014;0.92 during item deletion (<xref ref-type="table" rid="T1">Table 2</xref>).</p>
<table-wrap id="T2" position="float">
<label>TABLE 2</label>
<caption>
<p>Reliability and internal consistency.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="center">GMAS items</th>
<th align="center">Corrected ITC</th>
<th align="center">&#x3b1; if item deleted</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="center">1</td>
<td align="center">0.658</td>
<td align="center">0.898</td>
</tr>
<tr>
<td align="center">2</td>
<td align="center">0.744</td>
<td align="center">0.893</td>
</tr>
<tr>
<td align="center">3</td>
<td align="center">0.751</td>
<td align="center">0.893</td>
</tr>
<tr>
<td align="center">4</td>
<td align="center">0.736</td>
<td align="center">0.894</td>
</tr>
<tr>
<td align="center">5</td>
<td align="center">0.807</td>
<td align="center">0.890</td>
</tr>
<tr>
<td align="center">6</td>
<td align="center">0.638</td>
<td align="center">0.900</td>
</tr>
<tr>
<td align="center">7</td>
<td align="center">0.719</td>
<td align="center">0.895</td>
</tr>
<tr>
<td align="center">8</td>
<td align="center">0.792</td>
<td align="center">0.891</td>
</tr>
<tr>
<td align="center">9</td>
<td align="center">0.575</td>
<td align="center">0.903</td>
</tr>
<tr>
<td align="center">10</td>
<td align="center">0.523</td>
<td align="center">0.905</td>
</tr>
<tr>
<td align="center">11</td>
<td align="center">0.275</td>
<td align="center">0.920</td>
</tr>
</tbody>
</table>
</table-wrap>
</sec>
</sec>
<sec sec-type="discussion" id="s5">
<title>5 Discussion</title>
<p>A study by Awwad and others highlighted that most Jordanian patients had low adherence. In addition, it was highlighted in the study that education, monthly income, and knowledge of patients impact their adherence to medications (<xref ref-type="bibr" rid="B7">Awwad et al., 2015</xref>). Moreover, Basheti and others reported non-adherence in slightly less than half of their study population. Further, they establish a relationship between adherence score and comorbidity, number of medicines, etc. (<xref ref-type="bibr" rid="B8">Basheti et al., 2016</xref>). The current study reported a large proportion of patients to be adherent. However, due to the limited number of responses collected, it cannot be definitively confirmed if this outcome occurred by chance or represents a true pattern.</p>
<p>The validation process included several statistical approaches, such as CFA with SEM and evaluation of internal consistency through Cronbach&#x2019;s (&#x3b1;), ITC and &#x3b1; based on item deletion. The values for fit indices excluding RMSEA obtained in this study were &#x3e;0.95 for TLI and CFI, &#x3e;0.9 for GFI, and &#x3c;0.9 for AGFI. Usually, a value &#x3e;0.95 is considered excellent, while a value &#x3e;0.9 is considered acceptable (<xref ref-type="bibr" rid="B24">Sarmento and Costa, 2019</xref>). In addition, the value for RMSEA obtained in this study was &#x3c;0.08. Though a smaller value, such as &#x3c; 0.06, is appreciable for RMSEA, studies have provided 0.08 as a cut-off criterion as well (<xref ref-type="bibr" rid="B24">Sarmento and Costa, 2019</xref>). The GFI obtained in this study was 0.913 while AGFI was 0.860. Available evidence report that GFI and AGFI are considered as good if the value is close to 1.0. Also, the AGFI is always less than or equal to the GFI. Thus, based on the current literature the values for both were considered acceptable (<xref ref-type="bibr" rid="B11">Hayashi et al., 2011</xref>). In addition, the &#x3c7;<sup>2</sup>/df value obtained for this study was between one to two which is considered as good (<xref ref-type="bibr" rid="B24">Sarmento and Costa, 2019</xref>).</p>
<p>In comparison, the Mahmood and others in their validation study involving GMAS-AR in patients with diabetes in Sudan reported a &#x3c7;<sup>2</sup>/df value &#x3e;3, and CFI, TLI, GFI and AGFI &#x3e;0.9, while RMSEA was &#x3e;0.073. The value for Cronbach&#x2019;s &#x3b1; was 0.834 (<xref ref-type="bibr" rid="B15">Mahmoud et al., 2021</xref>). In addition, another study was conducted in Saudi Arabia in which Arabic version of GMAS was validated in patients with chronic ailments, reported a value &#x3e;0.95 for all fit indices and &#x3c;0.06 for RMSEA. A Cronbach&#x2019;s &#x3b1; value of 0.865 was reported (<xref ref-type="bibr" rid="B21">Naqvi et al., 2020a</xref>). In this study, the value Cronbach&#x2019;s &#x3b1; was reported at 0.907. Therefore, despite being small-scale compared to its predecessors, the results aligned with the previous two studies (<xref ref-type="bibr" rid="B21">Naqvi et al., 2020a</xref>; <xref ref-type="bibr" rid="B15">Mahmoud et al., 2021</xref>).</p>
<p>The CFA results provide support for the validity of the Arabic version of the GMAS in the studied population. The good fit of the model suggests that the scale adequately measures adherence based on the underlying constructs it is expected to measure. The factor loadings also substantiate that ability of the scale to measure adherence based on the expected factor structure. In addition, the item-total correlation values were positive and ranged from 0.275 to 0.807 with majority of items having corrected ITC &#x3e;0.5. This highlighted that each item in the questionnaire had a contributed positively towards measuring medication adherence and the scale had construct validity.</p>
<p>The availability of this scale for use in Jordanian patients would help clinicians to evaluate and monitor the pharmacotherapy of patients and would set an example for further investigation pertaining to the reliability and validity of GMAS in other disease populations in Jordan. The element of costing distinguishes this scale from the available instruments. It was observed in this study that slightly more than a third of patients paid for the medications out-of-pocket. Hence, this scale would enable the clinicians to evaluate the non-adherence due to the cost of medications as well.</p>
<p>The study was based on convenience sampling and was carried out in a single hospital. Besides, the number of surveys obtained was low. Based on these factors, some limitations of this study are identified. These aspects would affect the generalizability of results and may not represent the entire population. The risk of sampling error cannot be ruled out. This study may have low statistical power and may not be able to detect small and meaningful association between participants&#x2019; characteristics and their adherence score. As a result, sub-group analyses and multivariate regression analyses highlighting determinants of adherence could not be conducted on this dataset. Nevertheless, it satisfied the sampling requirements based on the statistical parameters for CFA analysis. However, the results pertaining to medication adherence and clinical information should not be generalized.</p>
</sec>
<sec sec-type="conclusion" id="s6">
<title>6 Conclusion</title>
<p>The results of this study highlight that the Arabic version of the GMAS is a reliable and valid tool to assess the medication adherence of patients with T2DM in Jordan. A new scale is now available for documenting adherence to medications in this population. This study also serves as a model for further validation the scale in other patient populations.</p>
</sec>
</body>
<back>
<sec sec-type="data-availability" id="s7">
<title>Data availability statement</title>
<p>The original contributions presented in the study are included in the article/<xref ref-type="sec" rid="s12">Supplementary Material</xref>, further inquiries can be directed to the corresponding author.</p>
</sec>
<sec id="s8">
<title>Ethics statement</title>
<p>The study involving humans was approved by Institutional Review Board of Jordan University of Science and Technology (Ref: 59/117/2018). The study was conducted in accordance with the local legislation and institutional requirements. The participants provided their written informed consent to participate in this study.</p>
</sec>
<sec id="s9">
<title>Author contributions</title>
<p>Study conception MI, FE-D, and AAN. Study design and methodology all authors, proposal writing and ethics approval QA, AN, and AAN. Questionnaire acquisition, addition of demographic variables AN, AAN, MI, and QA. Collection of data and entry in software AN, MI, and QA. Data cleaning, analyses MI. Result report writing MI, AAN, and AN. Manuscript writing all authors. MI, FE-D, AN, QA, and AAN. All authors contributed to the article and approved the submitted version.</p>
</sec>
<ack>
<p>This work is dedicated to the late Prof. Dr. Mohamed Azmi Hassali, our beloved mentor, colleague, and co-author. Special thanks to the pharmacy department for their cooperation and facilitation in the study.</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>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
</sec>
<sec id="s12">
<title>Supplementary material</title>
<p>The Supplementary Material for this article can be found online at: <ext-link ext-link-type="uri" xlink:href="https://www.frontiersin.org/articles/10.3389/fphar.2023.1194672/full#supplementary-material">https://www.frontiersin.org/articles/10.3389/fphar.2023.1194672/full&#x23;supplementary-material</ext-link>
</p>
<supplementary-material xlink:href="Table1.XLSX" id="SM1" mimetype="application/XLSX" xmlns:xlink="http://www.w3.org/1999/xlink"/>
</sec>
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