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<article xmlns:xlink="http://www.w3.org/1999/xlink" article-type="review-article" dtd-version="2.0">
  <front>
    <journal-meta>
      <journal-id journal-id-type="publisher-id">JMH</journal-id>
      <journal-id journal-id-type="nlm-ta">JMIR Ment Health</journal-id>
      <journal-title>JMIR Mental Health</journal-title>
      <issn pub-type="epub">2368-7959</issn>
      <publisher>
        <publisher-name>JMIR Publications</publisher-name>
        <publisher-loc>Toronto, Canada</publisher-loc>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="publisher-id">v11i1e48916</article-id>
      <article-id pub-id-type="pmid">38329804</article-id>
      <article-id pub-id-type="doi">10.2196/48916</article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Review</subject>
        </subj-group>
        <subj-group subj-group-type="article-type">
          <subject>Review</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Effectiveness and User Experience of Virtual Reality for Social Anxiety Disorder: Systematic Review</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="editor">
          <name>
            <surname>Torous</surname>
            <given-names>John</given-names>
          </name>
        </contrib>
      </contrib-group>
      <contrib-group>
        <contrib contrib-type="reviewer">
          <name>
            <surname>Triscari</surname>
            <given-names>Sergio</given-names>
          </name>
        </contrib>
        <contrib contrib-type="reviewer">
          <name>
            <surname>Xu</surname>
            <given-names>Qian</given-names>
          </name>
        </contrib>
        <contrib contrib-type="reviewer">
          <name>
            <surname>Benson</surname>
            <given-names>Nicole</given-names>
          </name>
        </contrib>
      </contrib-group>
      <contrib-group>
        <contrib id="contrib1" contrib-type="author">
          <name name-style="western">
            <surname>Shahid</surname>
            <given-names>Simon</given-names>
          </name>
          <degrees>BPsych, MPsych</degrees>
          <xref rid="aff1" ref-type="aff">1</xref>
          <ext-link ext-link-type="orcid">https://orcid.org/0009-0007-4635-8744</ext-link>
        </contrib>
        <contrib id="contrib2" contrib-type="author" corresp="yes">
          <name name-style="western">
            <surname>Kelson</surname>
            <given-names>Joshua</given-names>
          </name>
          <degrees>PhD</degrees>
          <xref rid="aff1" ref-type="aff">1</xref>
          <address>
            <institution>Faculty of Business, Justice, and Behavioural Sciences</institution>
            <institution>Charles Sturt University</institution>
            <addr-line>Panorama Ave</addr-line>
            <addr-line>Bathurst, 2795</addr-line>
            <country>Australia</country>
            <phone>61 2 6338 4570</phone>
            <email>jkelson@csu.edu.au</email>
          </address>
          <ext-link ext-link-type="orcid">https://orcid.org/0000-0002-3755-175X</ext-link>
        </contrib>
        <contrib id="contrib3" contrib-type="author">
          <name name-style="western">
            <surname>Saliba</surname>
            <given-names>Anthony</given-names>
          </name>
          <degrees>PhD</degrees>
          <xref rid="aff1" ref-type="aff">1</xref>
          <ext-link ext-link-type="orcid">https://orcid.org/0000-0002-4823-4602</ext-link>
        </contrib>
      </contrib-group>
      <aff id="aff1">
        <label>1</label>
        <institution>Faculty of Business, Justice, and Behavioural Sciences</institution>
        <institution>Charles Sturt University</institution>
        <addr-line>Bathurst</addr-line>
        <country>Australia</country>
      </aff>
      <author-notes>
        <corresp>Corresponding Author: Joshua Kelson <email>jkelson@csu.edu.au</email></corresp>
      </author-notes>
      <pub-date pub-type="collection">
        <year>2024</year>
      </pub-date>
      <pub-date pub-type="epub">
        <day>8</day>
        <month>2</month>
        <year>2024</year>
      </pub-date>
      <volume>11</volume>
      <elocation-id>e48916</elocation-id>
      <history>
        <date date-type="received">
          <day>21</day>
          <month>5</month>
          <year>2023</year>
        </date>
        <date date-type="rev-request">
          <day>30</day>
          <month>9</month>
          <year>2023</year>
        </date>
        <date date-type="rev-recd">
          <day>24</day>
          <month>11</month>
          <year>2023</year>
        </date>
        <date date-type="accepted">
          <day>5</day>
          <month>12</month>
          <year>2023</year>
        </date>
      </history>
      <copyright-statement>©Simon Shahid, Joshua Kelson, Anthony Saliba. Originally published in JMIR Mental Health (https://mental.jmir.org), 08.02.2024.</copyright-statement>
      <copyright-year>2024</copyright-year>
      <license license-type="open-access" xlink:href="https://creativecommons.org/licenses/by/4.0/">
        <p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in JMIR Mental Health, is properly cited. The complete bibliographic information, a link to the original publication on https://mental.jmir.org/, as well as this copyright and license information must be included.</p>
      </license>
      <self-uri xlink:href="https://mental.jmir.org/2024/1/e48916" xlink:type="simple"/>
      <abstract>
        <sec sec-type="background">
          <title>Background</title>
          <p>Social anxiety disorder (SAD) is a debilitating psychiatric disorder that affects occupational and social functioning. Virtual reality (VR) therapies can provide effective treatment for people with SAD. However, with rapid innovations in immersive VR technology, more contemporary research is required to examine the effectiveness and concomitant user experience outcomes (ie, safety, usability, acceptability, and attrition) of emerging VR interventions for SAD.</p>
        </sec>
        <sec sec-type="objective">
          <title>Objective</title>
          <p>The aim of this systematic review was to examine the effectiveness and user experience of contemporary VR interventions among people with SAD.</p>
        </sec>
        <sec sec-type="methods">
          <title>Methods</title>
          <p>The Cochrane Library, Emcare, PsycINFO, PubMed, ScienceDirect, Scopus, and Web of Science databases were searched between January 1, 2012, and April 26, 2022. Deduplicated search results were screened based on title and abstract information. Full-text examination was conducted on 71 articles. Studies of all designs and comparator groups were included if they appraised the effectiveness and user experience outcomes of any immersive VR intervention among people with SAD. A standardized coding sheet was used to extract data on key participant, intervention, comparator, outcome, and study design items.</p>
        </sec>
        <sec sec-type="results">
          <title>Results</title>
          <p>The findings were tabulated and discussed using a narrative synthesis. A total of 18 studies met the inclusion criteria.</p>
        </sec>
        <sec sec-type="conclusions">
          <title>Conclusions</title>
          <p>The findings showed that VR exposure therapy–based interventions can generally provide effective, safe, usable, and acceptable treatments for adults with SAD. The average attrition rate from VR treatment was low (11.36%) despite some reported user experience difficulties, including potential simulator sickness, exposure-based emotional distress, and problems with managing treatment delivered in a synchronous group setting. This review also revealed several research gaps, including a lack of VR treatment studies on children and adolescents with SAD as well as a paucity of standardized assessments of VR user experience interactions. More studies are required to address these issues.</p>
        </sec>
        <sec sec-type="Trial Registration">
          <title>Trial Registration</title>
          <p>PROSPERO CRD42022353891; https://www.crd.york.ac.uk/prospero/display_record.php?RecordID=353891</p>
        </sec>
      </abstract>
      <kwd-group>
        <kwd>social anxiety disorder</kwd>
        <kwd>social phobia</kwd>
        <kwd>virtual reality</kwd>
        <kwd>VR</kwd>
        <kwd>VR exposure therapy</kwd>
        <kwd>effectiveness</kwd>
        <kwd>user experience</kwd>
        <kwd>safety</kwd>
        <kwd>usability</kwd>
        <kwd>acceptability</kwd>
        <kwd>anxiety</kwd>
        <kwd>phobia</kwd>
        <kwd>exposure</kwd>
        <kwd>systematic</kwd>
        <kwd>review methods</kwd>
        <kwd>review methodology</kwd>
        <kwd>social</kwd>
        <kwd>psychiatric</kwd>
        <kwd>mental health</kwd>
        <kwd>mobile phone</kwd>
      </kwd-group>
    </article-meta>
  </front>
  <body>
    <sec sec-type="introduction">
      <title>Introduction</title>
      <sec>
        <title>Background</title>
        <p>Social anxiety disorder (SAD; also known as social phobia) is a psychiatric disorder that is distinguished by a fear of humiliation or negative evaluation by others [<xref ref-type="bibr" rid="ref1">1</xref>]. Current guidelines highlight the use of cognitive behavioral therapy to treat SAD [<xref ref-type="bibr" rid="ref2">2</xref>]. This can involve activities such as psychoeducation, relaxation, distraction, cognitive restructuring, exposure therapy, and relapse prevention [<xref ref-type="bibr" rid="ref2">2</xref>]. Despite the efficacy of cognitive behavioral therapy for SAD treatment [<xref ref-type="bibr" rid="ref3">3</xref>,<xref ref-type="bibr" rid="ref4">4</xref>], many who are diagnosed do not go on to seek help [<xref ref-type="bibr" rid="ref5">5</xref>]. This is partly due to the in vivo (real-life) nature of the exposure therapy used to desensitize and habituate patients to feared situations. It takes significant time, effort, and resources to accurately recreate scenarios that will incite an appropriate level of fear response in social settings [<xref ref-type="bibr" rid="ref6">6</xref>]. For example, to conduct in vivo exposure therapy with an individual with a fear of public speaking, a therapist would need to gather an audience in an appropriate context (ie, ensuring confidentiality and nonjudgment). Furthermore, social anxiety–provoking environments can be unpredictable, providing therapists with little control and a higher chance that a patient is embarrassed, leading to higher attrition rates [<xref ref-type="bibr" rid="ref7">7</xref>]. To potentially overcome these issues with delivering in vivo exposure therapy, some researchers have examined the use of virtual reality (VR) technology [<xref ref-type="bibr" rid="ref7">7</xref>].</p>
      </sec>
      <sec>
        <title>VR Technology</title>
        <p>VR technology provides a digital modality to deliver psychological interventions [<xref ref-type="bibr" rid="ref7">7</xref>,<xref ref-type="bibr" rid="ref8">8</xref>]. It involves the use of computer hardware and software technology (eg, stereoscopic displays of digital environments) to simulate real-world experiences [<xref ref-type="bibr" rid="ref7">7</xref>]. For instance, one may enter a virtual environment that mimics a physical environment and could adopt a virtual avatar to interact with this virtual environment [<xref ref-type="bibr" rid="ref9">9</xref>]. VR was first formulated in the 1960s, with the first commercial device developed in the 1980s [<xref ref-type="bibr" rid="ref10">10</xref>]. As technology has developed, the quality of images has improved, and costs have been reduced.</p>
        <p>VR systems can be divided into 2 categories: immersive and nonimmersive systems [<xref ref-type="bibr" rid="ref11">11</xref>]. Immersive systems, such as head-mounted displays (HMDs) or cave automatic virtual environments (CAVEs), provide users with a realistic experience of VR environments, whereas nonimmersive systems, such as computer monitors, result in users not feeling as present [<xref ref-type="bibr" rid="ref12">12</xref>]. Presence in VR refers to the extent of an individual’s perception of being in a particular environment [<xref ref-type="bibr" rid="ref13">13</xref>]. For VR therapy to be effective, an individual must feel present and immersed in the digital environment [<xref ref-type="bibr" rid="ref14">14</xref>]. A CAVE system consists of an empty room with multiple screens arranged in a cubelike formation with users wearing stereoscopic glasses and interacting with virtual objects projected onto the screens [<xref ref-type="bibr" rid="ref15">15</xref>]. Although CAVE systems have the potential to be more immersive than nonimmersive systems, they are expensive and complex to set up, require frequent physical and digital adjustments, and require dedicated personnel [<xref ref-type="bibr" rid="ref16">16</xref>]. Conversely, a recent systematic review found that current HMDs offer a more immersive experience than CAVEs and are significantly more user-friendly in cost and setup, with a “plug-n-play” setup solution [<xref ref-type="bibr" rid="ref15">15</xref>].</p>
        <p>When integrated with therapy, VR technology can help address factors that influence the success of exposure-based treatments. For instance, VR allows for the creation of controlled digital environments, which enables therapists to predictably customize exposure scenarios to the specific needs and fears of individual clients [<xref ref-type="bibr" rid="ref7">7</xref>]. VR can also improve accessibility to exposure therapy for individuals who find it logistically challenging or emotionally overwhelming to engage in real-world scenarios [<xref ref-type="bibr" rid="ref17">17</xref>]. The immersive nature of VR helps bridge the gap between simulated experiences and real-life situations, fostering a sense of presence and engagement that can potentially enhance treatment adherence and effectiveness [<xref ref-type="bibr" rid="ref17">17</xref>].</p>
      </sec>
      <sec>
        <title>Effectiveness of VR for SAD</title>
        <p>Virtual environments and avatars can be used to simulate socially distressing situations for SAD treatment. For example, a study immersed participants with SAD into a computer-generated classroom where they were asked to speak publicly on a topic while a therapist controlled the virtual audience’s reactions according to the stage of therapy [<xref ref-type="bibr" rid="ref18">18</xref>]. VR environments have also been shown to provide acceptable levels of presence and immersion that are necessary for exposure therapy in youth with social anxiety [<xref ref-type="bibr" rid="ref19">19</xref>]. Several systematic reviews and meta-analyses have demonstrated the effectiveness of VR exposure therapy (VRET) in the treatment of SAD [<xref ref-type="bibr" rid="ref6">6</xref>,<xref ref-type="bibr" rid="ref20">20</xref>-<xref ref-type="bibr" rid="ref24">24</xref>]. Indeed, researchers have established a large effect size for VRET versus waitlist (<italic>g</italic>=0.90), a medium to large effect size for VRET versus psychological placebo conditions (<italic>g</italic>=0.78) [<xref ref-type="bibr" rid="ref21">21</xref>], a large overall effect size for VRET (<italic>g</italic>=0.82) [<xref ref-type="bibr" rid="ref22">22</xref>], and a medium to large effect size for VRET at the 12-month follow-up (<italic>g</italic>=−0.74) [<xref ref-type="bibr" rid="ref6">6</xref>]. This consistent pattern of symptom reduction can be observed across various contexts, such as participant countries (eg, the United States, France, Israel, and South Korea) and treatment settings (eg, universities, hospitals, and clinics) [<xref ref-type="bibr" rid="ref6">6</xref>,<xref ref-type="bibr" rid="ref20">20</xref>-<xref ref-type="bibr" rid="ref24">24</xref>]. However, although existing reviews have explored VR-based therapy from an effectiveness standpoint (eg, reduction in anxiety symptoms), there are gaps in the literature on evaluating the VR user experience for people with SAD on key concomitant outcomes of safety, usability, acceptability, and attrition in different contexts.</p>
      </sec>
      <sec>
        <title>User Experience of VR for SAD</title>
        <sec>
          <title>Safety</title>
          <p>Studies using VR for workplace training, physical rehabilitation, psychological therapy, and other settings highlight a significant safety issue: simulator sickness [<xref ref-type="bibr" rid="ref25">25</xref>]. Simulator sickness (otherwise known as VR sickness or cybersickness) [<xref ref-type="bibr" rid="ref26">26</xref>-<xref ref-type="bibr" rid="ref28">28</xref>] is characterized by general discomfort, headache, eyestrain, nausea, difficulty concentrating, fatigue, blurred vision, dizziness, and vertigo. On the basis of postural instability theory, simulator sickness is arguably due to VR technology inducing sensory differences in the visual and vestibular systems, which coordinate balance and movement [<xref ref-type="bibr" rid="ref28">28</xref>-<xref ref-type="bibr" rid="ref30">30</xref>]. The human body may interpret these disparities as possibly deadly causes (ie, consuming poison) and seek to purge as a result [<xref ref-type="bibr" rid="ref25">25</xref>]. Consequently, simulator sickness can have a negative impact on participants during VR use and for hours following use [<xref ref-type="bibr" rid="ref31">31</xref>]. Other aspects of safety include physical injuries from repetitive strain, users colliding with objects in the real world, poor posture, headset discomfort, risk of inducing epileptic seizures, negative mood changes, and infection control [<xref ref-type="bibr" rid="ref32">32</xref>]. Overall, these issues might put participants at risk of harm or cause them to discontinue using VR. Thus, a comprehensive examination of VR safety for SAD is necessary.</p>
        </sec>
        <sec>
          <title>Usability</title>
          <p>There does not yet appear to be a framework for the evaluation of VR usability in therapy-based applications. Nielsen [<xref ref-type="bibr" rid="ref33">33</xref>] defines usability as a “quality attribute” that assesses how easy it is to interact with an interface. He highlighted 5 components: learnability (how easy it is for a beginner to use the interface), efficiency (once the user has learned to use the interface, how quickly they can perform tasks), memorability (re-establishing proficiency after a period of absence), errors (frequency, severity, and recoverability of errors), and satisfaction (level of pleasure from using the interface) [<xref ref-type="bibr" rid="ref33">33</xref>]. Although this framework is applied to website design, it can also be applied to participants’ perceptions of the usability of VR. Furthermore, the application of VR in real-world settings (eg, in a therapy room) would likely be performed by a clinician rather than a specialized technician. It is important to note that usability issues may arise among clinicians. For example, they may give up on the technology if components fail to load or connect to each other. For this reason, this review included both clinician experiences in administering VR-based therapy and client experiences.</p>
        </sec>
        <sec>
          <title>Acceptability</title>
          <p>Acceptability is a crucial consideration when evaluating VR interventions [<xref ref-type="bibr" rid="ref34">34</xref>]. It involves assessing the degree to which the new intervention and its components are received and aligned with the needs of the target population [<xref ref-type="bibr" rid="ref34">34</xref>]. For example, a study examining VR use in adults with SAD defined acceptability as a participant’s willingness to use a VR program [<xref ref-type="bibr" rid="ref35">35</xref>]. They measured acceptability by observing rates of attrition and responses to the following question—“Would you recommend this program to others who might have problems similar to yours?”—and inviting further feedback. Participants’ additional feedback was coded into 2 themes: satisfaction (sense of realism, insight, and utility) and perceived effects of the treatment (impact on anxiety). The findings indicated that VR was considered acceptable by participants on all measures [<xref ref-type="bibr" rid="ref35">35</xref>]. Nevertheless, although there are recent systematic reviews that have addressed the acceptability of VR use for the general population [<xref ref-type="bibr" rid="ref36">36</xref>], psychosis [<xref ref-type="bibr" rid="ref37">37</xref>], panic disorder [<xref ref-type="bibr" rid="ref38">38</xref>], and posttraumatic stress disorder [<xref ref-type="bibr" rid="ref39">39</xref>,<xref ref-type="bibr" rid="ref40">40</xref>], a review of the literature on the acceptability of VR in individuals with SAD does not yet exist based on our current knowledge.</p>
        </sec>
        <sec>
          <title>Attrition</title>
          <p>Attrition, the discontinuation of therapy before treatment completion and resolution of symptoms, can have profound negative effects [<xref ref-type="bibr" rid="ref41">41</xref>]. These can include the client not fully benefiting from therapy and being discouraged from seeking treatment in the future [<xref ref-type="bibr" rid="ref41">41</xref>] as well as the effect that this may have on the therapist (eg, loss of revenue, demoralization, and feelings of failure) [<xref ref-type="bibr" rid="ref42">42</xref>]. A recent meta-analysis of VRET showed significant heterogeneity in attrition rates in the treatment of anxiety disorders, highlighting reasons such as failure to immerse in the virtual environments, simulator sickness, vision complications, and difficulty communicating with a therapist that the participant could not see [<xref ref-type="bibr" rid="ref43">43</xref>]. A systematic review examining the available literature on rates of attrition of VR-based interventions (both VRET and non-VRET) with participants with SAD does not yet appear to exist based on our current knowledge.</p>
        </sec>
      </sec>
      <sec>
        <title>This Study</title>
        <p>This study aimed to systematically identify and review available evidence regarding the effectiveness and user experience (ie, safety, usability, acceptability, and rates of attrition) of VR interventions in the treatment of SAD. The following objectives aided in the provision of a comprehensive and up-to-date account of the empirical status of VR therapy for SAD: (1) provide an overview of the existing literature and identify areas in which further research is needed on the treatment of SAD; (2) assess the potential of using VR as a treatment option for SAD, specifically in terms of effectiveness and user experience; and (3) provide guidance and recommendations for future research regarding the use of VR as a treatment option for SAD.</p>
      </sec>
    </sec>
    <sec sec-type="methods">
      <title>Methods</title>
      <p>This systematic review was conducted using the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) checklist (<xref ref-type="supplementary-material" rid="app1">Multimedia Appendix 1</xref>) [<xref ref-type="bibr" rid="ref44">44</xref>]. The protocol of this systematic review was prospectively registered in the PROSPERO international database (CRD42022353891).</p>
      <sec>
        <title>Eligibility Criteria</title>
        <p>For articles to be included in this systematic review, the study participants needed to be people diagnosed with SAD regardless of age. If a study had a mix of people with and without SAD, that study would be included if subgroup analyses were available on the participants with SAD or if they made up the vast majority (ie, ≥80%). All studies needed to examine direct participant use of a VR intervention, which includes any system that incorporates immersive VR hardware (ie, HMD or CAVE systems). Only studies that were published after 2012 were included as this marked the introduction of widely available commercial HMD hardware such as the Oculus Rift [<xref ref-type="bibr" rid="ref9">9</xref>]. Such hardware allowed for the delivery of VR experiences comparable with previously expensive commercial setups at a cheaper cost as well as easier accessibility to researchers [<xref ref-type="bibr" rid="ref45">45</xref>]. Studies with research design comparators of any kind (eg, comparing VR with other non-VR interventions) were eligible for inclusion. All studies were required to report on VR intervention effectiveness and participant user engagement outcomes. This broadly included any standardized or unstandardized measure indicative of usability or acceptability (including attrition rates). Studies of all designs (ie, quantitative, qualitative, and mixed methods) were eligible for inclusion. No studies were excluded based on methodological quality. All the articles needed to be written in English and published in peer-reviewed journals.</p>
      </sec>
      <sec>
        <title>Search Strategy</title>
        <p>Prominent scientific research databases were searched between January 1, 2012, and April 26, 2022: Cochrane Library, Emcare, PsycINFO, PubMed, ScienceDirect, Scopus, and Web of Science. The following keywords were used to search the databases: (“virtual reality” or “VR”) and (“social anxiety” or “social phobia”). The reference lists of eligible articles were also searched.</p>
      </sec>
      <sec>
        <title>Article Selection</title>
        <p>The search results for all databases were deduplicated, and the remaining article titles and abstracts were scanned. Full-text appraisal was performed on promising articles, and the final study inclusion was agreed upon by the researchers using the eligibility criteria. Divergent views on inclusion were resolved through discussion and mutual agreement.</p>
      </sec>
      <sec>
        <title>Data Extraction</title>
        <p>Data from the included studies were extracted by one reviewer (SS) into a standardized coding sheet and then checked by a second reviewer (JK). The data types extracted from eligible papers included the following:</p>
        <list list-type="order">
          <list-item>
            <p>Reference source: author surnames, year of publication, and paper title.</p>
          </list-item>
          <list-item>
            <p>Sample: country; sample size; and nonidentifiable participant characteristics such as age, sex, and diagnosis.</p>
          </list-item>
          <list-item>
            <p>Study design: methodology, comparator trial arms, and measurement points (pretest, midtest, and posttest measurement and follow-up).</p>
          </list-item>
          <list-item>
            <p>VR intervention details: intervention program name, purpose of intervention (eg, exposure therapy, cognitive distraction, or relaxation), virtual environment type, hardware (eg, HMD or CAVE system), and treatment length.</p>
          </list-item>
          <list-item>
            <p>Effectiveness: standardized measure names, outcomes, and effect sizes.</p>
          </list-item>
          <list-item>
            <p>User experience: reported outcomes of intervention safety, usability, acceptability, attrition, and intention-to-treat analyses.</p>
          </list-item>
        </list>
        <p>Attrition in this review was defined and measured as the relative number of participants who began using the VR intervention but did not complete measurements during or after the intervention.</p>
      </sec>
      <sec>
        <title>Quality Assessment</title>
        <p>This systematic review included randomized controlled trial (RCT) and nonrandomized studies. Therefore, the Mixed Methods Appraisal Tool (MMAT) was used to assess the quality of all the included studies [<xref ref-type="bibr" rid="ref46">46</xref>]. The MMAT was used as it assesses methodological quality across 5 study categories: RCTs, nonrandomized quantitative studies, quantitative descriptive studies, qualitative studies, and mixed methods studies.</p>
      </sec>
      <sec>
        <title>Data Analysis</title>
        <p>A narrative synthesis approach was used in this systematic review. This involved summarizing and explaining the findings using text as a statistical meta-analysis was not possible because of data heterogeneity across the included studies.</p>
      </sec>
    </sec>
    <sec sec-type="results">
      <title>Results</title>
      <sec>
        <title>Study Selection</title>
        <p><xref rid="figure1" ref-type="fig">Figure 1</xref> shows that the literature search yielded 683 articles, of which 391 (57.2%) remained after deduplicating citations. Of these 391 records, 18 (4.6%) met the eligibility criteria.</p>
        <fig id="figure1" position="float">
          <label>Figure 1</label>
          <caption>
            <p>Flowchart of the systematic review search results. HMD: head-mounted display; SAD: social anxiety disorder.</p>
          </caption>
          <graphic xlink:href="mental_v11i1e48916_fig1.png" alt-version="no" mimetype="image" position="float" xlink:type="simple"/>
        </fig>
      </sec>
      <sec>
        <title>Participant Characteristics</title>
        <p>A total of 808 participants were recruited for the VR studies (<xref ref-type="table" rid="table1">Table 1</xref>). They were largely from South Korea (n=368), followed by the United States (n=163), the Netherlands (n=60), Canada (n=59), Sweden (n=23), Czech Republic (n=10), Denmark (n=9), and Brazil (n=2). The country of origin was missing for some participants (n=114). It is unclear whether participants were unique in 11% (2/18) of studies conducted by research teams with some of the same researchers [<xref ref-type="bibr" rid="ref47">47</xref>,<xref ref-type="bibr" rid="ref48">48</xref>]. The sample sizes ranged from 1 to 115 participants, with a median of 48 participants. Participants’ ages ranged from 18 to 65 years. Participants were mainly female, with an average sample proportion of 51.31% (SD 5.36%; range 0%-77.3%). Most participants were diagnosed with SAD. There were 9 participants with a diagnosis of flight phobia and 8 participants with a diagnosis of acrophobia; however, subgroup analyses were available for the participants with SAD in this study [<xref ref-type="bibr" rid="ref49">49</xref>]. All participant diagnoses were obtained through clinical interviews delivered in person, by phone, or via videoconferencing. In total, 3 therapists were interviewed in addition to the sample of participants in one study [<xref ref-type="bibr" rid="ref50">50</xref>].</p>
        <table-wrap position="float" id="table1">
          <label>Table 1</label>
          <caption>
            <p>Description of participants and research designs in the reviewed studies.</p>
          </caption>
          <table width="1000" cellpadding="5" cellspacing="0" border="1" rules="groups" frame="hsides">
            <col width="80"/>
            <col width="110"/>
            <col width="70"/>
            <col width="100"/>
            <col width="80"/>
            <col width="110"/>
            <col width="130"/>
            <col width="190"/>
            <col width="130"/>
            <thead>
              <tr valign="top">
                <td>Study</td>
                <td>Country</td>
                <td>Sample size<sup>a</sup></td>
                <td>Total sample mean age (years; SD)</td>
                <td>Total sample age range (years)</td>
                <td>Total sample percentage of female participants</td>
                <td>Study design</td>
                <td>Treatment conditions<sup>b</sup></td>
                <td>Measurements</td>
              </tr>
            </thead>
            <tbody>
              <tr valign="top">
                <td>Anderson et al [<xref ref-type="bibr" rid="ref51">51</xref>]</td>
                <td>United States</td>
                <td>97</td>
                <td>39.03 (11.26)</td>
                <td>19-69</td>
                <td>61.9</td>
                <td>RCT<sup>c</sup></td>
                <td>EGT<sup>d</sup>: 25; VRET<sup>e</sup>: 25; WL<sup>f</sup>: 25</td>
                <td>Pre- and posttest measurement and 3- and 12-month FU<sup>g</sup></td>
              </tr>
              <tr valign="top">
                <td>Arnfred et al [<xref ref-type="bibr" rid="ref50">50</xref>]</td>
                <td>Denmark</td>
                <td>9</td>
                <td>25.4 (6.54)</td>
                <td>19-35</td>
                <td>66.7</td>
                <td>Interview</td>
                <td>VRET: 9</td>
                <td>Posttest measurement</td>
              </tr>
              <tr valign="top">
                <td>Bouchard et al [<xref ref-type="bibr" rid="ref52">52</xref>]</td>
                <td>Canada</td>
                <td>59</td>
                <td>34.5 (11.9)</td>
                <td>18-65</td>
                <td>72.9</td>
                <td>RCT</td>
                <td>VRET: 17; in vivo: 22; WL: 20</td>
                <td>Pre- and posttest measurement and 6-month FU</td>
              </tr>
              <tr valign="top">
                <td>Geraets et al [<xref ref-type="bibr" rid="ref53">53</xref>]</td>
                <td>NR<sup>h</sup></td>
                <td>15</td>
                <td>34.9 (12.4)</td>
                <td>18-65</td>
                <td>53.3</td>
                <td>Single group</td>
                <td>VRET: 15</td>
                <td>Pre- and posttest measurement and 6-month FU</td>
              </tr>
              <tr valign="top">
                <td>Hur et al [<xref ref-type="bibr" rid="ref54">54</xref>]</td>
                <td>South Korea</td>
                <td>73</td>
                <td>NR</td>
                <td>NR</td>
                <td>42.6</td>
                <td>Case controlled</td>
                <td>VRET: 25; HC<sup>i</sup>: 22</td>
                <td>Pre- and posttest measurement</td>
              </tr>
              <tr valign="top">
                <td>Jeong et al [<xref ref-type="bibr" rid="ref55">55</xref>]</td>
                <td>South Korea</td>
                <td>115</td>
                <td>NR</td>
                <td>NR</td>
                <td>34.8</td>
                <td>Cohort</td>
                <td>ET<sup>j</sup>: 52; NT<sup>k</sup>: 43; SE<sup>l</sup>: 20</td>
                <td>Pre- and posttest measurement</td>
              </tr>
              <tr valign="top">
                <td>Kampmann et al [<xref ref-type="bibr" rid="ref56">56</xref>]</td>
                <td>The Netherlands</td>
                <td>60</td>
                <td>36.9</td>
                <td>18-65</td>
                <td>63.3</td>
                <td>RCT</td>
                <td>VRET: 20; WL: 20; iVET<sup>m</sup>: 20</td>
                <td>Pre- and posttest measurement and 3-month FU</td>
              </tr>
              <tr valign="top">
                <td>Kim et al [<xref ref-type="bibr" rid="ref47">47</xref>]</td>
                <td>South Korea</td>
                <td>54</td>
                <td>23</td>
                <td>NR</td>
                <td>57.7</td>
                <td>Controlled clinical trial</td>
                <td>VRET: 22; HC: 30</td>
                <td>Pre- and posttest measurement</td>
              </tr>
              <tr valign="top">
                <td>Kim et al [<xref ref-type="bibr" rid="ref57">57</xref>]</td>
                <td>South Korea</td>
                <td>74</td>
                <td>NR</td>
                <td>19-31</td>
                <td>56.9</td>
                <td>Longitudinal</td>
                <td>VRET: 32; HC: 33</td>
                <td>Pre- and posttest measurement</td>
              </tr>
              <tr valign="top">
                <td>Kim et al [<xref ref-type="bibr" rid="ref48">48</xref>]</td>
                <td>South Korea</td>
                <td>52</td>
                <td>NR</td>
                <td>19-30</td>
                <td>NR</td>
                <td>RCT</td>
                <td>VRS<sup>n</sup>: 24; WL: 28</td>
                <td>Pre- and posttest measurement</td>
              </tr>
              <tr valign="top">
                <td>Kovar [<xref ref-type="bibr" rid="ref58">58</xref>]</td>
                <td>Czech Republic</td>
                <td>10</td>
                <td>34.6 (11.7)</td>
                <td>19-51</td>
                <td>50</td>
                <td>Nonrandomized parallel comparison trial</td>
                <td>Psychotherapy: 5; psychotherapy+VRET: 5</td>
                <td>Pre- and posttest measurement</td>
              </tr>
              <tr valign="top">
                <td>Lindner et al [<xref ref-type="bibr" rid="ref59">59</xref>]</td>
                <td>Sweden</td>
                <td>23</td>
                <td>40.61 (10.15)</td>
                <td>≥18</td>
                <td>57</td>
                <td>Cohort</td>
                <td>VRET: 23</td>
                <td>Pre- and posttest measurement</td>
              </tr>
              <tr valign="top">
                <td>Moldovan and David [<xref ref-type="bibr" rid="ref49">49</xref>]</td>
                <td>NR</td>
                <td>32</td>
                <td>NR</td>
                <td>≥18</td>
                <td>46.9</td>
                <td>RCT</td>
                <td>VRCBT<sup>o</sup>: 16; WL: 16</td>
                <td>Pre- and posttest measurement and FU</td>
              </tr>
              <tr valign="top">
                <td>Perandré and Haydu [<xref ref-type="bibr" rid="ref60">60</xref>]</td>
                <td>Brazil</td>
                <td>2</td>
                <td>23.5 (4.9)</td>
                <td>20-27</td>
                <td>0</td>
                <td>Case study</td>
                <td>VRET: 2</td>
                <td>Pre- and posttest measurement and 1- and 3-month FU</td>
              </tr>
              <tr valign="top">
                <td>Price and Anderson [<xref ref-type="bibr" rid="ref61">61</xref>]</td>
                <td>NR</td>
                <td>67</td>
                <td>40.31 (11.55)</td>
                <td>NR</td>
                <td>69</td>
                <td>RCT</td>
                <td>VRET: 33; EGT: 34</td>
                <td>Pre-, mid-, and posttest measurement</td>
              </tr>
              <tr valign="top">
                <td>Rubin et al [<xref ref-type="bibr" rid="ref62">62</xref>]</td>
                <td>United States</td>
                <td>21</td>
                <td>NR</td>
                <td>18-65</td>
                <td>61.9</td>
                <td>RCT</td>
                <td>VRET: 10; VRET+AGT<sup>p</sup>: 11</td>
                <td>Pre- and posttest measurement and 1-week FU</td>
              </tr>
              <tr valign="top">
                <td>Trahan et al [<xref ref-type="bibr" rid="ref63">63</xref>]</td>
                <td>United States</td>
                <td>1</td>
                <td>36</td>
                <td>NR</td>
                <td>0</td>
                <td>Case study</td>
                <td>VRET: 1</td>
                <td>Pre- and posttest measurement</td>
              </tr>
              <tr valign="top">
                <td>Zainal et al [<xref ref-type="bibr" rid="ref64">64</xref>]</td>
                <td>United States</td>
                <td>44</td>
                <td>23.3 (9.32)</td>
                <td>18-53</td>
                <td>77.3</td>
                <td>RCT</td>
                <td>VRET: 26; WL: 18</td>
                <td>Pre- and posttest measurement and 3- and 6-month FU</td>
              </tr>
            </tbody>
          </table>
          <table-wrap-foot>
            <fn id="table1fn1">
              <p><sup>a</sup>Refers to the total number of participants in the study.</p>
            </fn>
            <fn id="table1fn2">
              <p><sup>b</sup>Refers to the number of participants in each treatment condition.</p>
            </fn>
            <fn id="table1fn3">
              <p><sup>c</sup>RCT: randomized controlled trial.</p>
            </fn>
            <fn id="table1fn4">
              <p><sup>d</sup>EGT: exposure group therapy.</p>
            </fn>
            <fn id="table1fn5">
              <p><sup>e</sup>VRET: virtual reality exposure therapy.</p>
            </fn>
            <fn id="table1fn6">
              <p><sup>f</sup>WL: waitlist control.</p>
            </fn>
            <fn id="table1fn7">
              <p><sup>g</sup>FU: follow-up.</p>
            </fn>
            <fn id="table1fn8">
              <p><sup>h</sup>NR: not reported.</p>
            </fn>
            <fn id="table1fn9">
              <p><sup>i</sup>HC: healthy controls.</p>
            </fn>
            <fn id="table1fn10">
              <p><sup>j</sup>ET: early termination.</p>
            </fn>
            <fn id="table1fn11">
              <p><sup>k</sup>NT: normal termination.</p>
            </fn>
            <fn id="table1fn12">
              <p><sup>l</sup>SE: session extension.</p>
            </fn>
            <fn id="table1fn13">
              <p><sup>m</sup>iVET: in vivo exposure therapy.</p>
            </fn>
            <fn id="table1fn14">
              <p><sup>n</sup>VRS: virtual reality self-training.</p>
            </fn>
            <fn id="table1fn15">
              <p><sup>o</sup>VRCBT: virtual reality cognitive behavioral therapy.</p>
            </fn>
            <fn id="table1fn16">
              <p><sup>p</sup>AGT: attention guidance training.</p>
            </fn>
          </table-wrap-foot>
        </table-wrap>
      </sec>
      <sec>
        <title>Details of the VR Interventions</title>
        <p>All the studies included VR-based exposure therapy. Nearly all the studies (15/18, 83%) tested a unique VR intervention except for the studies by Jeong et al [<xref ref-type="bibr" rid="ref55">55</xref>] and Kim et al [<xref ref-type="bibr" rid="ref47">47</xref>,<xref ref-type="bibr" rid="ref48">48</xref>] (<xref ref-type="table" rid="table2">Table 2</xref>). VR hardware included standard computers, smartphones, and HMDs. In total, 17% (3/18) of the studies [<xref ref-type="bibr" rid="ref49">49</xref>,<xref ref-type="bibr" rid="ref51">51</xref>,<xref ref-type="bibr" rid="ref61">61</xref>] did not identify the headset brands. The studies used custom-built software that immersed participants in VR environments that simulated social situations increasing in difficulty with audio, video, text, and interactivity. The treatment lengths ranged from 1 to 14 sessions of exposure therapy, with a mode of 8. A total of 17% (3/18) of the studies [<xref ref-type="bibr" rid="ref53">53</xref>,<xref ref-type="bibr" rid="ref55">55</xref>,<xref ref-type="bibr" rid="ref64">64</xref>] terminated the sessions early if habituation occurred before the completion of the sessions. Participant VR use time ranged from 5 minutes to 3 hours per session, and 17% (3/18) of the studies delivered the VR in a single session [<xref ref-type="bibr" rid="ref49">49</xref>,<xref ref-type="bibr" rid="ref59">59</xref>,<xref ref-type="bibr" rid="ref62">62</xref>]. All VR interventions were tested with therapist or facilitator guidance even though 22% (4/18) [<xref ref-type="bibr" rid="ref47">47</xref>,<xref ref-type="bibr" rid="ref48">48</xref>,<xref ref-type="bibr" rid="ref55">55</xref>,<xref ref-type="bibr" rid="ref64">64</xref>] were designed to be delivered as self-help.</p>
        <table-wrap position="float" id="table2">
          <label>Table 2</label>
          <caption>
            <p>Details of the virtual reality (VR) interventions.</p>
          </caption>
          <table width="1000" cellpadding="5" cellspacing="0" border="1" rules="groups" frame="hsides">
            <col width="170"/>
            <col width="400"/>
            <col width="170"/>
            <col width="260"/>
            <thead>
              <tr valign="top">
                <td>Study</td>
                <td>Virtual environments</td>
                <td>Headset</td>
                <td>Treatment length (duration)</td>
              </tr>
            </thead>
            <tbody>
              <tr valign="top">
                <td>Anderson et al [<xref ref-type="bibr" rid="ref51">51</xref>]</td>
                <td>Conference room, classroom, and auditorium</td>
                <td>—<sup>a</sup></td>
                <td>4 exposure sessions (30 min each)</td>
              </tr>
              <tr valign="top">
                <td>Arnfred et al [<xref ref-type="bibr" rid="ref50">50</xref>]</td>
                <td>Supermarket, meeting, cafeteria, party, and auditorium</td>
                <td>Oculus Go</td>
                <td>8 exposure sessions (45 min each)</td>
              </tr>
              <tr valign="top">
                <td>Bouchard et al [<xref ref-type="bibr" rid="ref52">52</xref>]</td>
                <td>Meeting room, job interview, apartment, coffee shop, neighbors, store, and neutral</td>
                <td>eMagin Z800</td>
                <td>8 exposure sessions (20-30 min each)</td>
              </tr>
              <tr valign="top">
                <td>Geraets et al [<xref ref-type="bibr" rid="ref53">53</xref>]</td>
                <td>Street, bus, café, and supermarket</td>
                <td>Sony HMZ-T1</td>
                <td>14 exposure sessions (40 min each)</td>
              </tr>
              <tr valign="top">
                <td>Hur et al [<xref ref-type="bibr" rid="ref54">54</xref>]</td>
                <td>College student group</td>
                <td>HTC Vive</td>
                <td>6 exposure sessions (5-8 min each)</td>
              </tr>
              <tr valign="top">
                <td>Jeong et al [<xref ref-type="bibr" rid="ref55">55</xref>]</td>
                <td>School, business, and daily life</td>
                <td>Samsung Gear VR powered by Oculus</td>
                <td>ET<sup>b</sup> (1-8 exposure sessions); NT<sup>c</sup> (9-10 exposure sessions); SE<sup>d</sup> (11-17 exposure sessions)</td>
              </tr>
              <tr valign="top">
                <td>Kampmann et al [<xref ref-type="bibr" rid="ref56">56</xref>]</td>
                <td>Audience, stranger, clothes shopping, job interview, journalist interview, restaurant, and blind date</td>
                <td>nVisor SX</td>
                <td>7 exposure sessions (60 min each)</td>
              </tr>
              <tr valign="top">
                <td>Kim et al [<xref ref-type="bibr" rid="ref47">47</xref>]</td>
                <td>School, business, and daily life</td>
                <td>Samsung Gear VR powered by Oculus</td>
                <td>8 exposure sessions</td>
              </tr>
              <tr valign="top">
                <td>Kim et al [<xref ref-type="bibr" rid="ref57">57</xref>]</td>
                <td>College student group</td>
                <td>HTC Vive</td>
                <td>6 exposure sessions</td>
              </tr>
              <tr valign="top">
                <td>Kim et al [<xref ref-type="bibr" rid="ref48">48</xref>]</td>
                <td>School, business, and daily life</td>
                <td>Samsung Gear VR powered by Oculus</td>
                <td>8 exposure sessions</td>
              </tr>
              <tr valign="top">
                <td>Kovar [<xref ref-type="bibr" rid="ref58">58</xref>]</td>
                <td>Public speaking, telephone call, receiving criticism, job interview, refusal of job offer or unwanted product, and working lunch</td>
                <td>HTC Vive</td>
                <td>8 exposure sessions</td>
              </tr>
              <tr valign="top">
                <td>Lindner et al [<xref ref-type="bibr" rid="ref59">59</xref>]</td>
                <td>Board room, conference room, and classroom</td>
                <td>Oculus Go</td>
                <td>1 exposure session (180 min)</td>
              </tr>
              <tr valign="top">
                <td>Moldovan and David [<xref ref-type="bibr" rid="ref49">49</xref>]</td>
                <td>Presentation and interview</td>
                <td>—</td>
                <td>1 exposure session (90 min)</td>
              </tr>
              <tr valign="top">
                <td>Perandré and Haydu [<xref ref-type="bibr" rid="ref60">60</xref>]</td>
                <td>Food court in shopping center</td>
                <td>Oculus Rift</td>
                <td>8 exposure sessions</td>
              </tr>
              <tr valign="top">
                <td>Price and Anderson [<xref ref-type="bibr" rid="ref61">61</xref>]</td>
                <td>Conference room, classroom, and auditorium</td>
                <td>—</td>
                <td>8 exposure sessions</td>
              </tr>
              <tr valign="top">
                <td>Rubin et al [<xref ref-type="bibr" rid="ref62">62</xref>]</td>
                <td>Conference room and auditorium</td>
                <td>Oculus Rift DK2</td>
                <td>1 exposure session (45 min)</td>
              </tr>
              <tr valign="top">
                <td>Trahan et al [<xref ref-type="bibr" rid="ref63">63</xref>]</td>
                <td>Grocery store</td>
                <td>Plastic HMD<sup>e</sup> bracket for mobile phone</td>
                <td>12 exposure sessions (12-15 min each)</td>
              </tr>
              <tr valign="top">
                <td>Zainal et al [<xref ref-type="bibr" rid="ref64">64</xref>]</td>
                <td>Dinner party and job interview</td>
                <td>Pico Goblin VR</td>
                <td>8 exposure sessions (25-30 min each)</td>
              </tr>
            </tbody>
          </table>
          <table-wrap-foot>
            <fn id="table2fn1">
              <p><sup>a</sup>Brand not reported.</p>
            </fn>
            <fn id="table2fn2">
              <p><sup>b</sup>ET: early termination.</p>
            </fn>
            <fn id="table2fn3">
              <p><sup>c</sup>NT: normal termination.</p>
            </fn>
            <fn id="table2fn4">
              <p><sup>d</sup>SE: session extension.</p>
            </fn>
            <fn id="table2fn5">
              <p><sup>e</sup>HMD: head-mounted display.</p>
            </fn>
          </table-wrap-foot>
        </table-wrap>
      </sec>
      <sec>
        <title>Research Designs and Comparators</title>
        <p><xref ref-type="table" rid="table1">Table 1</xref> summarizes the research designs and comparators. Nearly half (8/18, 44%) of the studies appraised participant VR use through RCT designs. Comparators included exposure group therapy, in vivo exposure, early and extended termination, attention guidance training using VR, psychotherapy, and waitlist control. All studies (18/18, 100%) had pre- and posttest assessments of user outcomes, although 39% (7/18) also had follow-up assessments, with the longest being 12 months [<xref ref-type="bibr" rid="ref51">51</xref>].</p>
      </sec>
      <sec>
        <title>Effectiveness Measures and Outcomes</title>
        <p>The details of the effectiveness measures and outcomes of VR treatment for SAD are summarized in <xref ref-type="table" rid="table3">Table 3</xref>. VR treatment effect sizes across all studies that reported them ranged from medium to large. Almost all studies (15/18, 83%) demonstrated a decrease in symptoms following VR treatment.</p>
        <table-wrap position="float" id="table3">
          <label>Table 3</label>
          <caption>
            <p>Details on social anxiety measures and virtual reality (VR) effectiveness outcomes.</p>
          </caption>
          <table width="1000" cellpadding="5" cellspacing="0" border="1" rules="groups" frame="hsides">
            <col width="30"/>
            <col width="160"/>
            <col width="810"/>
            <thead>
              <tr valign="top">
                <td colspan="2">Study and measures</td>
                <td>VR effectiveness outcomes</td>
              </tr>
            </thead>
            <tbody>
              <tr valign="top">
                <td colspan="3">
                  <bold>Anderson et al [<xref ref-type="bibr" rid="ref51">51</xref>]</bold>
                </td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>PRCS<sup>a</sup></td>
                <td>Significant improvement in confidence as a speaker from before to after treatment (<italic>d</italic><sup>b</sup>=1.19; <italic>P</italic>=.01), with benefits maintained at the 3- and 6-month follow-ups.</td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>FNE-B<sup>c</sup></td>
                <td>Significant decrease in fear of negative evaluation from before to after treatment (<italic>d</italic><italic>=</italic>0.29; <italic>P</italic>=.01), with benefits maintained at the 3- and 6-month follow-ups.</td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>BAT<sup>d</sup></td>
                <td>Significant improvement in speech length (<italic>d</italic>=0.78; <italic>P</italic>=.01) and peak anxiety (<italic>d</italic>=0.70; <italic>P</italic>=.02) from before to after treatment.</td>
              </tr>
              <tr valign="top">
                <td colspan="3">
                  <bold>Arnfred et al [<xref ref-type="bibr" rid="ref50">50</xref>]</bold>
                </td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>NSQ<sup>e</sup></td>
                <td>The virtual environments effectively induced immersion and anxiety in some but not all participants with social anxiety disorder.</td>
              </tr>
              <tr valign="top">
                <td colspan="3">
                  <bold>Bouchard et al [<xref ref-type="bibr" rid="ref52">52</xref>]</bold>
                </td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>LSAS-SR<sup>f</sup></td>
                <td>Significant decrease in social anxiety symptoms from before to after treatment compared with waitlist (<italic>P</italic>&#60;.001) that was maintained at the 6-month follow-up.</td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>BAT</td>
                <td>Significant decrease in behavioral avoidance from before to after treatment (<italic>P</italic>&#60;.001).</td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>SPS<sup>g</sup></td>
                <td>Significant decrease in social phobia from before to after treatment (<italic>P</italic>&#60;.001) that was maintained at the 6-month follow-up.</td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>SIAS<sup>h</sup></td>
                <td>Significant decrease in social anxiety symptoms from before to after treatment (<italic>P</italic>&#60;.001) that was maintained at the 6-month follow-up.</td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>FNE<sup>i</sup></td>
                <td>Significant decrease in fear of negative evaluation from before to after treatment (<italic>P</italic>&#60;.001) that was maintained at the 6-month follow-up.</td>
              </tr>
              <tr valign="top">
                <td colspan="3">
                  <bold>Geraets et al [<xref ref-type="bibr" rid="ref53">53</xref>]</bold>
                </td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>SIAS</td>
                <td>Significant decrease in social interaction anxiety from before to after treatment (<italic>d</italic>=0.9; <italic>P</italic>=.008) that was maintained at the 6-month follow-up (<italic>d</italic>=1.3; <italic>P</italic>=.003).</td>
              </tr>
              <tr valign="top">
                <td colspan="3">
                  <bold>Hur et al [<xref ref-type="bibr" rid="ref54">54</xref>]</bold>
                </td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>SPS</td>
                <td>Significant decrease in social phobia symptoms from before to after treatment (<italic>P</italic>=.005).</td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>PERS<sup>j</sup></td>
                <td>Significant decrease in negative postevent rumination from before to after treatment (<italic>P</italic>&#60;.001).</td>
              </tr>
              <tr valign="top">
                <td colspan="3">
                  <bold>Jeong et al [<xref ref-type="bibr" rid="ref55">55</xref>]</bold>
                </td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>FNE-B</td>
                <td>Significant decrease in fear of negative evaluation from first to last session for the early, normal, and extended termination groups (<italic>P</italic>&#60;.001).</td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>LSAS</td>
                <td>Significant decrease in social anxiety symptoms from first to last session for the normal (<italic>P</italic>&#60;.001) and extended termination groups (<italic>P</italic>=.002).</td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>SPS</td>
                <td>Significant decrease in social phobia symptoms from first to last session for the normal (<italic>P</italic>=.001) and extended termination groups (<italic>P</italic>&#60;.001).</td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>SIAS</td>
                <td>Significant decrease in social interaction anxiety from first to last session for the normal (<italic>P</italic>&#60;.001) and extended termination groups (<italic>P</italic>=.006).</td>
              </tr>
              <tr valign="top">
                <td colspan="3">
                  <bold>Kampmann et al [<xref ref-type="bibr" rid="ref56">56</xref>]</bold>
                </td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>LSAS-SR</td>
                <td>Significant decrease in social anxiety symptoms from before to after treatment compared with waitlist (<italic>d</italic>=0.55; <italic>P</italic>=.01) that was maintained at the 3-month follow-up.</td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>FNE-B</td>
                <td>No significant change in fear of negative evaluation compared with waitlist group from before to after treatment or the 3-month follow-up.</td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>BAT</td>
                <td>Significant increase in speech length from before to after treatment compared with waitlist (<italic>d</italic>=0.56; <italic>P</italic>=.02) that was maintained at the 3-month follow-up; however, there was no significant difference in speech performance.</td>
              </tr>
              <tr valign="top">
                <td colspan="3">
                  <bold>Kim et al [<xref ref-type="bibr" rid="ref47">47</xref>]</bold>
                </td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>HADS<sup>k</sup></td>
                <td>Significant decrease in anxiety symptoms from before to after treatment (<italic>P</italic>&#60;.001).</td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>LSAS-SR</td>
                <td>Significant decrease in social anxiety symptoms from before to after treatment (<italic>P</italic>&#60;.001).</td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>SIAS</td>
                <td>Significant decrease in social interaction anxiety from before to after treatment (<italic>P</italic>&#60;.001).</td>
              </tr>
              <tr valign="top">
                <td colspan="3">
                  <bold>Kim et al [<xref ref-type="bibr" rid="ref57">57</xref>]</bold>
                </td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>SPS</td>
                <td>Significant decrease in social phobia symptoms from before to after treatment (<italic>P</italic>&#60;.001).</td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>SIAS</td>
                <td>Significant decrease in social interaction anxiety from before to after treatment (<italic>P</italic>&#60;.001).</td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>FNE-B</td>
                <td>Significant decrease in fear of negative evaluation from before to after treatment (<italic>P</italic>=.004).</td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>KSAD<sup>l</sup></td>
                <td>Significant decrease in social avoidance and distress from before to after treatment (<italic>P</italic>&#60;.001).</td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>LSAS<sup>m</sup></td>
                <td>Significant decrease in social anxiety symptoms from before to after treatment (<italic>P</italic>=.04).</td>
              </tr>
              <tr valign="top">
                <td colspan="3">
                  <bold>Kim et al [<xref ref-type="bibr" rid="ref48">48</xref>]</bold>
                </td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>HADS</td>
                <td>No significant changes in anxiety symptoms from before to after treatment.</td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>LSAS-SR</td>
                <td>Significant decrease in social anxiety symptoms from before to after treatment (<italic>P</italic>&#60;.01).</td>
              </tr>
              <tr valign="top">
                <td colspan="3">
                  <bold>Kovar [<xref ref-type="bibr" rid="ref58">58</xref>]</bold>
                </td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>FNE-B, SPIN<sup>n</sup>, SIAS, SADS<sup>o</sup>, and BAI<sup>p</sup></td>
                <td>Higher average decrease in symptoms on all these measures in the VR treatment group compared with the non-VR treatment group.</td>
              </tr>
              <tr valign="top">
                <td colspan="3">
                  <bold>Lindner et al [<xref ref-type="bibr" rid="ref59">59</xref>]</bold>
                </td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>PSAS<sup>q</sup></td>
                <td>Significant decrease in self-rated public speaking anxiety following the first 3-hour session (<italic>d</italic>=0.77; <italic>P</italic>=.006).</td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>LSAS-SR</td>
                <td>Significant decrease in social anxiety symptoms from before to after treatment (<italic>P</italic>=.001).</td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>FNE-B</td>
                <td>Significant decrease in fear of negative evaluation from before to after treatment (<italic>P</italic>=.04).</td>
              </tr>
              <tr valign="top">
                <td colspan="3">
                  <bold>Moldovan and Price [<xref ref-type="bibr" rid="ref49">49</xref>]</bold>
                </td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>FNE-B</td>
                <td>Significant decrease in fear of negative evaluation from before to after treatment (<italic>P</italic>&#60;.05).</td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>SSPS<sup>r</sup></td>
                <td>Significant decrease in negative self-statements from before to after treatment (<italic>P</italic>&#60;.05).</td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>LSAS</td>
                <td>Significant decrease in social anxiety symptoms from before to after treatment (<italic>P</italic>&#60;.05).</td>
              </tr>
              <tr valign="top">
                <td colspan="3">
                  <bold>Perandré and Haydu [<xref ref-type="bibr" rid="ref60">60</xref>]</bold>
                </td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>SPIN and BAI</td>
                <td>Decrease in anxiety symptoms reported on both measures from the pretest measurement to the 3-month follow-up from treatment for both participants.</td>
              </tr>
              <tr valign="top">
                <td colspan="3">
                  <bold>Price and Anderson [<xref ref-type="bibr" rid="ref61">61</xref>]</bold>
                </td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>SSPS</td>
                <td>Significant improvements on positive and negative self-statements from before to after treatment (<italic>P</italic>&#60;.01).</td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>PRCA-SF<sup>s</sup></td>
                <td>Significant decrease in public speaking anxiety from before to after treatment (<italic>P</italic>&#60;.01).</td>
              </tr>
              <tr valign="top">
                <td colspan="3">
                  <bold>Rubin et al [<xref ref-type="bibr" rid="ref62">62</xref>]</bold>
                </td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>PRPSA<sup>t</sup></td>
                <td>Significant decrease in fear of public speaking from before to after treatment (<italic>d</italic>=−1.11) and at the 1-week follow-up (<italic>d</italic>=−1.68).</td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>LSAS-SR</td>
                <td>Significant decrease in general symptoms of social anxiety from before to after treatment (<italic>d</italic>=−0.60) and at the 1-week follow-up (<italic>d</italic>=−2.07).</td>
              </tr>
              <tr valign="top">
                <td colspan="3">
                  <bold>Trahan et al [<xref ref-type="bibr" rid="ref63">63</xref>]</bold>
                </td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>SUDS<sup>u</sup></td>
                <td>No significant change in subjective distress from before to after treatment for the participant (<italic>P</italic>=.21).</td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>SADS</td>
                <td>Score decrease of 52.6% in social anxiety from before to after treatment for the participant.</td>
              </tr>
              <tr valign="top">
                <td colspan="3">
                  <bold>Zainal et al [<xref ref-type="bibr" rid="ref64">64</xref>]</bold>
                </td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>SAD composite<sup>v</sup></td>
                <td>Significant decrease in social anxiety symptoms from before to after treatment compared with the waitlist group (<italic>g</italic><sup>w</sup>=−4.77; <italic>P</italic>&#60;.001). No significant within-group change at the 3- (<italic>g</italic>=0.12) and 6-month follow-ups (<italic>g</italic>=−0.13).</td>
              </tr>
              <tr valign="top">
                <td>
                  <break/>
                </td>
                <td>MASI<sup>x</sup></td>
                <td>Significant decrease in job interview anxiety from before to after treatment compared with the waitlist group (<italic>g</italic>=−4.17; <italic>P</italic>&#60;.001). No significant within-group change at the 3- (<italic>g</italic>=−0.10) and 6-month follow-ups (<italic>g</italic>=−0.53).</td>
              </tr>
            </tbody>
          </table>
          <table-wrap-foot>
            <fn id="table3fn1">
              <p><sup>a</sup>PRCS: Personal Report of Confidence as a Speaker.</p>
            </fn>
            <fn id="table3fn2">
              <p><sup>b</sup>Cohen <italic>d</italic> effect size.</p>
            </fn>
            <fn id="table3fn3">
              <p><sup>c</sup>FNE-B: brief Fear of Negative Evaluation Scale.</p>
            </fn>
            <fn id="table3fn4">
              <p><sup>d</sup>BAT: behavioral avoidance task.</p>
            </fn>
            <fn id="table3fn5">
              <p><sup>e</sup>NSQ: nonstandardized questions.</p>
            </fn>
            <fn id="table3fn6">
              <p><sup>f</sup>LSAS-SR: Liebowitz Social Anxiety Scale–Self-Report.</p>
            </fn>
            <fn id="table3fn7">
              <p><sup>g</sup>SPS: Social Phobia Scale.</p>
            </fn>
            <fn id="table3fn8">
              <p><sup>h</sup>SIAS: Social Interaction Anxiety Scale.</p>
            </fn>
            <fn id="table3fn9">
              <p><sup>i</sup>FNE: Fear of Negative Evaluation Scale.</p>
            </fn>
            <fn id="table3fn10">
              <p><sup>j</sup>PERS: Post-Event Rumination Scale.</p>
            </fn>
            <fn id="table3fn11">
              <p><sup>k</sup>HADS: Hospital Anxiety and Depression Scale.</p>
            </fn>
            <fn id="table3fn12">
              <p><sup>l</sup>KSAD: Korean Social Avoidance and Distress Scale.</p>
            </fn>
            <fn id="table3fn13">
              <p><sup>m</sup>LSAS: Liebowitz Social Anxiety Scale.</p>
            </fn>
            <fn id="table3fn14">
              <p><sup>n</sup>SPIN: Social Phobia Inventory.</p>
            </fn>
            <fn id="table3fn15">
              <p><sup>o</sup>SADS: Social Avoidance and Distress Scale.</p>
            </fn>
            <fn id="table3fn16">
              <p><sup>p</sup>BAI: Beck Anxiety Inventory.</p>
            </fn>
            <fn id="table3fn17">
              <p><sup>q</sup>PSAS: Public Speaking Anxiety Scale.</p>
            </fn>
            <fn id="table3fn18">
              <p><sup>r</sup>SSPS: Self-Statements During Public Speaking scale.</p>
            </fn>
            <fn id="table3fn19">
              <p><sup>s</sup>PRCA-SF: Personal Report of Communication Apprehension–Short Form.</p>
            </fn>
            <fn id="table3fn20">
              <p><sup>t</sup>PRPSA: Personal Report of Public Speaking Anxiety.</p>
            </fn>
            <fn id="table3fn21">
              <p><sup>u</sup>SUDS: Subjective Units of Distress Scale.</p>
            </fn>
            <fn id="table3fn22">
              <p><sup>v</sup>SAD composite: average standardized scores of the Social Phobia Diagnostic Questionnaire and the SIAS.</p>
            </fn>
            <fn id="table3fn23">
              <p><sup>w</sup>Hedges <italic>g</italic> effect size.</p>
            </fn>
            <fn id="table3fn24">
              <p><sup>x</sup>MASI: Measure of Anxiety in Selection Interviews.</p>
            </fn>
          </table-wrap-foot>
        </table-wrap>
      </sec>
      <sec>
        <title>User Experience With the VR Interventions</title>
        <p>The average attrition rate was 11.36% across all studies in the active VR treatment phase, with a range of 0% to 45.2% (<xref ref-type="table" rid="table4">Table 4</xref>). A total of 22% (4/18) of the studies reported the use of an intention-to-treat analysis. To measure VR user experience, 56% (10/18) of the studies used standardized measures, and 11% (2/18) of the studies used nonstandardized questions. A total of 67% (8/12) of these studies reported positive VR user experience findings in various areas of presence, usability, acceptability, or satisfaction. Low levels of simulator sickness were reported in 75% (3/4) of the studies that used standardized questions; however, 25% (1/4) of these studies reported higher levels of simulator sickness in participants with SAD than in controls without SAD [<xref ref-type="bibr" rid="ref47">47</xref>]. No other safety issues, such as physical injury, user collision, postural complaints, headset discomfort, seizures, or infection, were reported.</p>
        <table-wrap position="float" id="table4">
          <label>Table 4</label>
          <caption>
            <p>Virtual reality (VR) interventions and user experience outcomes.</p>
          </caption>
          <table width="1000" cellpadding="5" cellspacing="0" border="1" rules="groups" frame="hsides">
            <col width="130"/>
            <col width="100"/>
            <col width="600"/>
            <col width="100"/>
            <col width="70"/>
            <thead>
              <tr valign="top">
                <td>Study</td>
                <td>Measures</td>
                <td>VR user experience findings</td>
                <td>Attrition (%)</td>
                <td>ITT<sup>a</sup></td>
              </tr>
            </thead>
            <tbody>
              <tr valign="top">
                <td>Anderson et al [<xref ref-type="bibr" rid="ref51">51</xref>]</td>
                <td>CSQ<sup>b</sup></td>
                <td>High satisfaction with VR was reported after treatment and maintained at the 12-month follow-up.</td>
                <td>5/30 (17)</td>
                <td>Yes</td>
              </tr>
              <tr valign="top">
                <td>Arnfred et al [<xref ref-type="bibr" rid="ref50">50</xref>]</td>
                <td>NSQ<sup>c</sup></td>
                <td>A high level of presence in virtual environments for some participants but not all. There were technical issues with setting up and storing away equipment for the group. Wearing the HMD<sup>d</sup> in front of strangers was more anxiety provoking than the virtual environments for some participants. All patients found VR to be a meaningful addition to their therapy sessions, with several wanting more exposure.</td>
                <td>0/9 (0)</td>
                <td>—<sup>e</sup></td>
              </tr>
              <tr valign="top">
                <td>Bouchard et al [<xref ref-type="bibr" rid="ref52">52</xref>]</td>
                <td>SSQ<sup>f</sup>, PQ<sup>g</sup>, and GPQ<sup>h</sup></td>
                <td>No significant increases in simulator sickness after exposure sessions (<italic>P</italic>&#62;.20). Good level of presence that increased with a higher number of exposures.</td>
                <td>2/17 (12)</td>
                <td>Yes</td>
              </tr>
              <tr valign="top">
                <td>Geraets et al [<xref ref-type="bibr" rid="ref53">53</xref>]</td>
                <td>—</td>
                <td>VR treatment was well tolerated and deemed acceptable for most participants.</td>
                <td>2/15 (13)</td>
                <td>—</td>
              </tr>
              <tr valign="top">
                <td>Hur et al [<xref ref-type="bibr" rid="ref54">54</xref>]</td>
                <td>—</td>
                <td>—</td>
                <td>16/73 (21)</td>
                <td>—</td>
              </tr>
              <tr valign="top">
                <td>Jeong et al [<xref ref-type="bibr" rid="ref55">55</xref>]</td>
                <td>—</td>
                <td>—</td>
                <td>52/115 (45)</td>
                <td>—</td>
              </tr>
              <tr valign="top">
                <td>Kampmann et al [<xref ref-type="bibr" rid="ref56">56</xref>]</td>
                <td>—</td>
                <td>Simulator sickness led one patient to drop out.</td>
                <td>5/20 (25)</td>
                <td>Yes</td>
              </tr>
              <tr valign="top">
                <td>Kim et al [<xref ref-type="bibr" rid="ref47">47</xref>]</td>
                <td>SSQ</td>
                <td>Participants with SAD<sup>i</sup> experienced significantly more simulator sickness than participants without SAD (<italic>P</italic>=.003).</td>
                <td>2/54 (4)</td>
                <td>—</td>
              </tr>
              <tr valign="top">
                <td>Kim et al [<xref ref-type="bibr" rid="ref57">57</xref>]</td>
                <td>—</td>
                <td>—</td>
                <td>9/74 (12)</td>
                <td>—</td>
              </tr>
              <tr valign="top">
                <td>Kim et al [<xref ref-type="bibr" rid="ref48">48</xref>]</td>
                <td>SSQ</td>
                <td>Low levels of simulator sickness.</td>
                <td>3/24 (13)</td>
                <td>—</td>
              </tr>
              <tr valign="top">
                <td>Kovar [<xref ref-type="bibr" rid="ref58">58</xref>]</td>
                <td>—</td>
                <td>—</td>
                <td>0/10 (0)</td>
                <td>—</td>
              </tr>
              <tr valign="top">
                <td>Lindner et al [<xref ref-type="bibr" rid="ref59">59</xref>]</td>
                <td>NEQ<sup>j</sup></td>
                <td>High stress levels and low levels of satisfaction.</td>
                <td>3/23 (13)</td>
                <td>Yes</td>
              </tr>
              <tr valign="top">
                <td>Moldovan and David [<xref ref-type="bibr" rid="ref49">49</xref>]</td>
                <td>ITQ<sup>k</sup> and PQ</td>
                <td>No moderating effect of immersion and presence on pre- and posttest anxiety.</td>
                <td>0/32 (0)</td>
                <td>—</td>
              </tr>
              <tr valign="top">
                <td>Perandré and Haydu [<xref ref-type="bibr" rid="ref60">60</xref>]</td>
                <td>SPI<sup>l</sup></td>
                <td>High sense of presence reported by both participants.</td>
                <td>0/2 (0)</td>
                <td>—</td>
              </tr>
              <tr valign="top">
                <td>Price and Anderson [<xref ref-type="bibr" rid="ref61">61</xref>]</td>
                <td>—</td>
                <td>From a randomly selected subset of videotaped sessions (14%), high participant compliance was found, with 92% of the VR treatment protocol being completed.</td>
                <td>0/33 (0)</td>
                <td>—</td>
              </tr>
              <tr valign="top">
                <td>Rubin et al [<xref ref-type="bibr" rid="ref62">62</xref>]</td>
                <td>—</td>
                <td>—</td>
                <td>2/21 (10)</td>
                <td>—</td>
              </tr>
              <tr valign="top">
                <td>Trahan et al [<xref ref-type="bibr" rid="ref63">63</xref>]</td>
                <td>SUS<sup>m</sup></td>
                <td>High usability reported by the participant.</td>
                <td>0/1 (0)</td>
                <td>—</td>
              </tr>
              <tr valign="top">
                <td>Zainal et al [<xref ref-type="bibr" rid="ref64">64</xref>]</td>
                <td>NSQ, IPQ<sup>n</sup>, and SSQ</td>
                <td>Acceptable presence and low levels of simulator sickness. High levels of homework compliance. Participants (85%) would recommend it to others with SAD. High levels of acceptability and usability.</td>
                <td>9/44 (21)</td>
                <td>—</td>
              </tr>
            </tbody>
          </table>
          <table-wrap-foot>
            <fn id="table4fn1">
              <p><sup>a</sup>ITT: intention-to-treat analysis.</p>
            </fn>
            <fn id="table4fn2">
              <p><sup>b</sup>CSQ: Client Satisfaction Questionnaire.</p>
            </fn>
            <fn id="table4fn3">
              <p><sup>c</sup>NSQ: nonstandardized questions.</p>
            </fn>
            <fn id="table4fn4">
              <p><sup>d</sup>HMD: head-mounted display.</p>
            </fn>
            <fn id="table4fn5">
              <p><sup>e</sup>Not reported.</p>
            </fn>
            <fn id="table4fn6">
              <p><sup>f</sup>SSQ: Simulator Sickness Questionnaire.</p>
            </fn>
            <fn id="table4fn7">
              <p><sup>g</sup>PQ: Presence Questionnaire.</p>
            </fn>
            <fn id="table4fn8">
              <p><sup>h</sup>GPQ: Gatineau Presence Questionnaire.</p>
            </fn>
            <fn id="table4fn9">
              <p><sup>i</sup>SAD: social anxiety disorder.</p>
            </fn>
            <fn id="table4fn10">
              <p><sup>j</sup>NEQ: Negative Effects Questionnaire.</p>
            </fn>
            <fn id="table4fn11">
              <p><sup>k</sup>ITQ: Immersive Tendencies Questionnaire.</p>
            </fn>
            <fn id="table4fn12">
              <p><sup>l</sup>SPI: Sense of Presence Inventory.</p>
            </fn>
            <fn id="table4fn13">
              <p><sup>m</sup>SUS: System Usability Scale.</p>
            </fn>
            <fn id="table4fn14">
              <p><sup>n</sup>IPQ: Igroup Presence Questionnaire.</p>
            </fn>
          </table-wrap-foot>
        </table-wrap>
      </sec>
      <sec>
        <title>Quality Assessment Results</title>
        <p><xref ref-type="supplementary-material" rid="app2">Multimedia Appendix 2</xref> [<xref ref-type="bibr" rid="ref47">47</xref>-<xref ref-type="bibr" rid="ref64">64</xref>] contains a table of quality assessment results for the included studies. In all RCT studies [<xref ref-type="bibr" rid="ref48">48</xref>,<xref ref-type="bibr" rid="ref49">49</xref>,<xref ref-type="bibr" rid="ref51">51</xref>,<xref ref-type="bibr" rid="ref52">52</xref>,<xref ref-type="bibr" rid="ref56">56</xref>,<xref ref-type="bibr" rid="ref61">61</xref>,<xref ref-type="bibr" rid="ref62">62</xref>,<xref ref-type="bibr" rid="ref64">64</xref>], randomization was reported, but schedule details were unclear in 11% (2/18) of the studies [<xref ref-type="bibr" rid="ref48">48</xref>,<xref ref-type="bibr" rid="ref61">61</xref>]. All RCT studies reported comparable baseline group analyses. In total, 38% (3/8) of the RCT studies reported complete outcome data, which is defined as ≥80% [<xref ref-type="bibr" rid="ref49">49</xref>,<xref ref-type="bibr" rid="ref56">56</xref>,<xref ref-type="bibr" rid="ref64">64</xref>]. All but the RCT studies by Kim et al [<xref ref-type="bibr" rid="ref48">48</xref>], Moldovan and David [<xref ref-type="bibr" rid="ref49">49</xref>], Price and Anderson [<xref ref-type="bibr" rid="ref61">61</xref>], and Rubin et al [<xref ref-type="bibr" rid="ref62">62</xref>] reported blinding of outcome assessors, which was applied at the pretest measurements. All RCT studies except those by Bouchard et al [<xref ref-type="bibr" rid="ref52">52</xref>], Kampmann et al [<xref ref-type="bibr" rid="ref56">56</xref>], and Rubin et al [<xref ref-type="bibr" rid="ref62">62</xref>] reported that participants adhered to their assigned VR interventions.</p>
        <p>In the quantitative descriptive studies [<xref ref-type="bibr" rid="ref53">53</xref>,<xref ref-type="bibr" rid="ref60">60</xref>,<xref ref-type="bibr" rid="ref63">63</xref>], the sampling strategy was relevant to the research question except in 33% (1/3) of the studies, in which details were unclear [<xref ref-type="bibr" rid="ref53">53</xref>]. All quantitative descriptive study samples were representative of the target population, and the measures fulfilled the inclusion criteria. Nonresponse bias was low in all studies except one (2/3, 67%) [<xref ref-type="bibr" rid="ref60">60</xref>]. Statistical analyses were appropriate to answer the research question in 33% (1/3) of the studies [<xref ref-type="bibr" rid="ref53">53</xref>] but unclear in the other 2 [<xref ref-type="bibr" rid="ref60">60</xref>,<xref ref-type="bibr" rid="ref63">63</xref>].</p>
        <p>In the quantitative nonrandomized studies [<xref ref-type="bibr" rid="ref47">47</xref>,<xref ref-type="bibr" rid="ref54">54</xref>,<xref ref-type="bibr" rid="ref55">55</xref>,<xref ref-type="bibr" rid="ref57">57</xref>-<xref ref-type="bibr" rid="ref59">59</xref>], participants were representative of the target population, measurements were appropriate regarding both the outcome and intervention, and there were complete outcome data (defined as ≥80%) in all but 2 studies (4/6, 67%) [<xref ref-type="bibr" rid="ref54">54</xref>,<xref ref-type="bibr" rid="ref55">55</xref>]. Confounds were accounted for in the design and analysis of 50% (3/6) of the studies [<xref ref-type="bibr" rid="ref54">54</xref>,<xref ref-type="bibr" rid="ref55">55</xref>,<xref ref-type="bibr" rid="ref59">59</xref>]. In total, 67% (2/3) of the quantitative nonrandomized studies reported that the intervention was administered as intended [<xref ref-type="bibr" rid="ref54">54</xref>,<xref ref-type="bibr" rid="ref55">55</xref>].</p>
        <p>In the single qualitative interview study [<xref ref-type="bibr" rid="ref50">50</xref>], the qualitative approach was appropriate to answer the research question; the data collection methods were adequate to address the research question; findings were adequately derived from the data; the interpretation of the results was sufficiently substantiated by the data; and there was coherence between qualitative data sources, collection, analysis, and interpretation.</p>
      </sec>
    </sec>
    <sec sec-type="discussion">
      <title>Discussion</title>
      <sec>
        <title>Principal Findings</title>
        <sec>
          <title>Overview</title>
          <p>SAD is a common and debilitating anxiety disorder that affects occupational and social functioning [<xref ref-type="bibr" rid="ref2">2</xref>]. Current in vivo–based exposure therapies require significant time, resources, and effort, which results in limited treatment dissemination [<xref ref-type="bibr" rid="ref6">6</xref>]. VR technology provides an alternative modality for treating SAD [<xref ref-type="bibr" rid="ref19">19</xref>]; however, contemporary evidence on the user experience of VR for SAD is sparse. This systematic review was conducted to provide a comprehensive and up-to-date account of the available evidence regarding the effectiveness and user experience (ie, safety, usability, acceptability, and attrition) of VR interventions for the treatment of SAD.</p>
        </sec>
        <sec>
          <title>Effectiveness of VR Interventions for SAD</title>
          <p>Our review found that VR interventions can effectively treat SAD in adult populations, which is congruent with the existing literature [<xref ref-type="bibr" rid="ref6">6</xref>,<xref ref-type="bibr" rid="ref20">20</xref>-<xref ref-type="bibr" rid="ref24">24</xref>]. It is interesting to note that, although our search terms and inclusion criteria were open to any VR-based intervention for treating people with SAD (eg, providing relaxation, cognitive distraction, exposure therapy, and psychoeducation), all the included interventions were intended for exposure therapy. This indicates that VRET dominates the research field of VR-based interventions for SAD.</p>
          <p>Studies including follow-up measures highlight the maintenance of SAD symptom improvement from 1 week [<xref ref-type="bibr" rid="ref62">62</xref>] to 1 year [<xref ref-type="bibr" rid="ref51">51</xref>], indicating that VRET can provide effective short- and long-term treatment for SAD symptoms. This is impressive given that the study showing maintained benefits for up to 1 year involved only 4 treatment sessions [<xref ref-type="bibr" rid="ref51">51</xref>]. However, it is important to note that this study only included participants with a fear of public speaking as the primary social fear as opposed to other social situations (eg, going to dinner with friends), limiting the generalizability of the findings [<xref ref-type="bibr" rid="ref65">65</xref>]. Nevertheless, our findings suggest that VRET can be a rapidly effective treatment for SAD with the potential to provide long-term symptom improvement.</p>
        </sec>
        <sec>
          <title>Safety of VR Interventions for SAD</title>
          <p>Simulator sickness was a common measure of safety in the reviewed studies. Participant simulator sickness was reportedly low in most studies. However, it was found that participants with an SAD diagnosis were more prone to simulator sickness when compared with participants without SAD in one study [<xref ref-type="bibr" rid="ref47">47</xref>]. This could be because patients with anxiety tend to experience greater motion discomfort [<xref ref-type="bibr" rid="ref66">66</xref>,<xref ref-type="bibr" rid="ref67">67</xref>]. For example, patients with anxiety may be more susceptible to irregular breathing and hyperventilation, leading to dizziness and nausea when exposed to fear-inducing cues. This may exacerbate the body’s interpretation of disparities in visual and vestibular systems as possible deadly causes (ie, poison) and potentially lead to nausea and vomiting [<xref ref-type="bibr" rid="ref25">25</xref>]. Another safety consideration is the absence of other physical injuries (eg, collisions with real-world objects, poor posture, headset discomfort, and seizures) reported in the reviewed studies, which supports VR as a safe SAD treatment.</p>
          <p>However, although the research safety findings are encouraging, the limitations of these studies are important to note. For example, most studies screened out participants who were unable to tolerate the VR environment and HMD or those who had a history of seizures. This would result in a sampling bias in favor of VR safety. Furthermore, all studies except for one [<xref ref-type="bibr" rid="ref63">63</xref>] were conducted in controlled settings (ie, hospitals and clinics) that were supervised by clinicians, further reducing risks that would otherwise be significant when using VR alone. For example, an individual purchasing and using a VR system at home may collide with real-world objects without the intervention of a third party. As such, more research is required to evaluate the safety of VR for SAD in nonclinical, unsupervised settings.</p>
        </sec>
        <sec>
          <title>Usability of VR Interventions for SAD</title>
          <p>There was large variability in the VR software used for SAD. This is likely due to the infancy of VR for SAD. With such variability, it is inevitable that reports of usability will vary according to the hardware and software used, with some programs being easier to use than others.</p>
          <p>A distinct hindrance in evaluating the usability of VR for SAD was the lack of an existing framework. The studies largely used nonstandardized questions and qualitative feedback to determine usability, making it difficult to generalize findings across multiple studies. Although most studies did not comment on aspects of usability, those that did provided valuable information on the usability of VR for SAD. Studies in which practitioners delivered VR therapy to individual participants reported high levels of usability, such as the ease of setting up and navigating the hardware and software. However, reports of VR use in a group setting described low levels of usability, significant amounts of time spent on setting up and storing the equipment, and loss of focus on the exposure experience when therapists were helping others with their HMDs [<xref ref-type="bibr" rid="ref50">50</xref>].</p>
          <p>The differences in usability between individualized and group settings highlight important requirements for the use of VR interventions for SAD. Primarily, VR technology for SAD needs to be easy to learn by patients, and it is important that errors are limited in frequency and severity and that patients can recover from errors largely autonomously. As such, we propose a “VR usability framework” for the measurement of usability of VR for SAD that borrows elements from the usability heuristics by Nielsen [<xref ref-type="bibr" rid="ref33">33</xref>]: (1) “learnability,” assessing how easy it is for a patient to set up and learn the VR technology; (2) “errors,” assessing the frequency, severity, and recoverability of errors autonomously by the patient; and (3) “memorability,” how easy it is to re-establish proficiency after a period of absence.</p>
          <p>Using the VR usability framework, current trends show variability in the usability of VR for SAD. VR used in group therapy has a steep learning curve and requires substantial input from therapists to work through errors, and it is difficult to re-establish proficiency in it after a period of absence (eg, some participants wished they could take the equipment home) [<xref ref-type="bibr" rid="ref50">50</xref>]. In contrast, VR used in individualized therapy is easy to learn, patients can autonomously handle errors, and they are familiar with the technology upon return [<xref ref-type="bibr" rid="ref63">63</xref>,<xref ref-type="bibr" rid="ref64">64</xref>]. Thus, VR may be more user-friendly in one-on-one therapy as opposed to a group setting, as articulated by the VR usability framework.</p>
        </sec>
        <sec>
          <title>Acceptability of VR Interventions for SAD</title>
          <p>The results we found regarding high VR acceptability in adult patients with SAD are congruent with earlier research by Saxena [<xref ref-type="bibr" rid="ref35">35</xref>]. Empirical findings indicate that VR for SAD is generally acceptable to adult patients with SAD, with high scores on standardized measures of satisfaction reported by most patients. Positive qualitative responses suggest that VR allowed patients to gain more insights into their anxiety and a better understanding of the social situations that they would normally avoid or be too emotionally activated to observe [<xref ref-type="bibr" rid="ref50">50</xref>]. For example, in real life, an individual with social anxiety may avoidantly play with their phone when someone sits next to them in a cafeteria rather than perceive the encounter as a valued learning experience. Therefore, it is likely that many adults with SAD who willingly undergo VR therapy will find the experience acceptable.</p>
          <p>Conversely, one study [<xref ref-type="bibr" rid="ref59">59</xref>] found that some patients reported that their expectations for the treatment were not fulfilled, and some reported feeling more stress during VR. It was also found that positive expectations of VR effectiveness as well as a positive working alliance with the therapist were significantly correlated with positive emotional changes [<xref ref-type="bibr" rid="ref49">49</xref>]. Therefore, VR treatment may not be acceptable for all adults with SAD based on individual differences regarding their previous VR experience, their perceptions of VR therapy helpfulness, their level of distress tolerance to exposure to digital stimuli before habituation [<xref ref-type="bibr" rid="ref68">68</xref>], and the nature of their relationship with the therapist offering VR treatment.</p>
        </sec>
        <sec>
          <title>Attrition of VR Interventions for SAD</title>
          <p>This review found that the attrition rate across most studies was relatively low and within acceptable levels (≤20%) [<xref ref-type="bibr" rid="ref46">46</xref>]. Indeed, attrition rates for the use of VR interventions for SAD were found to be substantially lower than estimates from VRET in anxiety disorders [<xref ref-type="bibr" rid="ref43">43</xref>]. Considering this, it appears that patients with SAD continue with treatment more than other patients with anxiety.</p>
          <p>There may be several reasons for the low average attrition rate finding. First, patients with SAD may prefer to learn more about social situations in a VR space. An individual with SAD may be curious about learning about social situations but may struggle to overcome the anxiety associated with placing themselves in an environment where negative evaluation is possible. By engaging with VR, patients with SAD have the knowledge that they can exit the simulation at any point, giving them the opportunity to learn about social situations without real-world social consequences. Second, patients with SAD may be more tolerant of the potentially negative effects of VR (eg, simulator sickness) when compared with the general population with anxiety [<xref ref-type="bibr" rid="ref43">43</xref>]. Third, patients with SAD may be more hesitant to drop out of therapy for fear of negative evaluation by examiners. For instance, patients with SAD may be more likely to remain in a study because of social desirability bias—the tendency to respond in a certain way to avoid criticism [<xref ref-type="bibr" rid="ref69">69</xref>].</p>
          <p>It is important to note that the observed attrition rates are heterogeneous. Some studies reported proportionally higher attrition rates than others [<xref ref-type="bibr" rid="ref54">54</xref>,<xref ref-type="bibr" rid="ref55">55</xref>]. This may be due to the differences in the number of sessions involved in different studies. For example, some studies were composed of single sessions [<xref ref-type="bibr" rid="ref49">49</xref>,<xref ref-type="bibr" rid="ref59">59</xref>,<xref ref-type="bibr" rid="ref62">62</xref>], whereas the study with the highest attrition had 9 to 17 sessions [<xref ref-type="bibr" rid="ref55">55</xref>]. As it takes longer to deliver all sessions, there is more opportunity for participants to drop out. Furthermore, attrition was defined in this review as those who did not complete measurements during or after intervention use, including completion of follow-up measures. Considering that some studies included follow-up measures of 3 months after the intervention or longer, it is plausible that participants may not have re-engaged in these measures for several reasons. These could potentially include both therapy-related factors (eg, intolerance of VR-induced anxiety, simulator sickness, and low satisfaction levels) or factors outside of therapy (eg, moving away, becoming too busy in everyday life, and major life events).</p>
        </sec>
      </sec>
      <sec>
        <title>Recommendations</title>
        <sec>
          <title>Safety</title>
          <p>With regard to safety, the primary issue identified in this review was simulator sickness. Several factors appear to be related to the susceptibility to simulator sickness. If simulator sickness is exacerbated by physiological symptoms of anxiety (eg, hyperventilation leading to dizziness) [<xref ref-type="bibr" rid="ref66">66</xref>,<xref ref-type="bibr" rid="ref67">67</xref>], it may be helpful to target these symptoms with clinical treatment before using VR technology. This is in line with other studies exploring attrition in anxiety disorders [<xref ref-type="bibr" rid="ref43">43</xref>], which found that VRET attrition occurs early in treatment because of factors such as dizziness. As such, VR protocols for SAD should aim to improve retention at the beginning of treatment using a phase-based approach that includes strategies to tolerate negative emotions before immersion in VR. These may include implementation of relaxation and grounding techniques [<xref ref-type="bibr" rid="ref70">70</xref>] or the prescription of antinausea medications. Changes in VR technology can also be applied to reduce simulator sickness [<xref ref-type="bibr" rid="ref48">48</xref>]. Blurring or lowering the resolution of a VR image has been shown to reduce simulator sickness and improve the sense of reality [<xref ref-type="bibr" rid="ref71">71</xref>,<xref ref-type="bibr" rid="ref72">72</xref>].</p>
        </sec>
        <sec>
          <title>Future Research</title>
          <p>Presently, there are many research gaps in the literature regarding the user experience of VR for SAD. The development of a standardized measure to assess the usability of VR for SAD has the potential to identify prominent issues with usability and aid in the development of future VR programs. This measure may include elements identified in the VR usability framework discussed previously to assess learnability, error recoverability, and memorability. This may be applied to technical developments in VR that would likely improve VR’s “plug-n-play” capability for SAD and other anxiety disorder treatments. Future research should also delve deeper into the study of simulator sickness in patients with SAD when compared with both healthy controls and patients with other anxiety disorders. This may lead to valuable information on reducing simulator sickness, thereby reducing the levels of attrition and improving the user experience of VR for SAD. Finally, there were no studies found that specifically targeted a child or adolescent population. Given that the onset of SAD typically occurs around adolescence [<xref ref-type="bibr" rid="ref1">1</xref>], future studies should evaluate the efficacy of early intervention of VR for SAD, particularly given adolescents’ success with VR for psychological distress [<xref ref-type="bibr" rid="ref32">32</xref>].</p>
        </sec>
      </sec>
      <sec>
        <title>Limitations</title>
        <p>This review has several limitations. First, our review did not perform a cost-benefit analysis of the hardware identified (eg, HMDs). Affordability could have implications for the acceptability of VR among consumers with SAD. Second, we included only English-language studies, and there may have been pertinent articles published in other languages. Third, this study conducted a qualitative review of studies with different designs. Although the MMAT [<xref ref-type="bibr" rid="ref46">46</xref>] was used to assess the quality of the studies, there is still a risk of subjective reviewer bias in addressing its criteria. Finally, studies may have been missed in our search because of obscure nomenclature (eg, research publications that did not clearly specify the use of a VR intervention for SAD in their title and abstract).</p>
      </sec>
      <sec>
        <title>Conclusions</title>
        <p>Our review findings showed that VRET interventions can generally provide an effective, safe, usable, acceptable, and low-attrition treatment option for adults with SAD. Nevertheless, there are research gaps evident when appraising user experience outcomes. These include the need to conduct more VR research with children and adolescents with SAD. We also do not yet know the specific causes of elevated simulator sickness in patients with SAD compared with participants without SAD or how effective other VR-based interventions beyond exposure therapy (eg, focused on mindfulness, relaxation, or cognitive distraction) are in the treatment of SAD. Further experimental studies (eg, pilot feasibility studies and RCTs) are required to explore these domains.</p>
      </sec>
    </sec>
  </body>
  <back>
    <app-group>
      <supplementary-material id="app1">
        <label>Multimedia Appendix 1</label>
        <p>PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) 2009 checklist.</p>
        <media xlink:href="mental_v11i1e48916_app1.pdf" xlink:title="PDF File  (Adobe PDF File), 146 KB"/>
      </supplementary-material>
      <supplementary-material id="app2">
        <label>Multimedia Appendix 2</label>
        <p>Quality assessment results of the included studies.</p>
        <media xlink:href="mental_v11i1e48916_app2.pdf" xlink:title="PDF File  (Adobe PDF File), 174 KB"/>
      </supplementary-material>
    </app-group>
    <glossary>
      <title>Abbreviations</title>
      <def-list>
        <def-item>
          <term id="abb1">CAVE</term>
          <def>
            <p>cave automatic virtual environment</p>
          </def>
        </def-item>
        <def-item>
          <term id="abb2">HMD</term>
          <def>
            <p>head-mounted display</p>
          </def>
        </def-item>
        <def-item>
          <term id="abb3">MMAT</term>
          <def>
            <p>Mixed Methods Appraisal Tool</p>
          </def>
        </def-item>
        <def-item>
          <term id="abb4">PRISMA</term>
          <def>
            <p>Preferred Reporting Items for Systematic Reviews and Meta-Analyses</p>
          </def>
        </def-item>
        <def-item>
          <term id="abb5">RCT</term>
          <def>
            <p>randomized controlled trial</p>
          </def>
        </def-item>
        <def-item>
          <term id="abb6">SAD</term>
          <def>
            <p>social anxiety disorder</p>
          </def>
        </def-item>
        <def-item>
          <term id="abb7">VR</term>
          <def>
            <p>virtual reality</p>
          </def>
        </def-item>
        <def-item>
          <term id="abb8">VRET</term>
          <def>
            <p>virtual reality exposure therapy</p>
          </def>
        </def-item>
      </def-list>
    </glossary>
    <ack>
      <p>The authors acknowledge the financial support provided by Charles Sturt University.</p>
    </ack>
    <fn-group>
      <fn fn-type="conflict">
        <p>None declared.</p>
      </fn>
    </fn-group>
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