Validity and Reliability of Mixed Reality-Based Performance Tests in Overweight and Obese Adults
2026年6月12日 更新者：Mehmet Kaan ALTUNOK、Selcuk University
Validity and Reliability of the Mixed Reality Adaptation of Performance Tests in Overweight and Obese Individuals
This study aims to evaluate the validity and reliability of mixed reality (MR)-based adaptations of functional mobility and performance tests developed using the Meta Quest 3 platform by comparing their outcomes with conventional clinical assessments. Virtual and mixed reality technologies have gained increasing attention in clinical measurement due to their potential advantages, including assessment standardization, enhanced user interaction, and automated data collection.
Previous studies have demonstrated that virtual reality-based performance assessments can provide high reliability and show meaningful associations with traditional clinical measures across different populations. However, visual and vestibular stimuli, depth perception, and changes in movement strategies may cause performance in virtual environments to differ from performance in conventional settings. Therefore, the validity and reliability of each virtual or mixed reality adaptation should be established within the target population.
Overweight and obese individuals exhibit biomechanical and physiological characteristics that may affect balance, gait mechanics, joint loading, and physical performance. Consequently, measurement properties established in other populations cannot be assumed to apply directly to overweight and obese individuals. In addition, factors related to head-mounted displays and motion-tracking systems may influence assessment outcomes.
The purpose of this study is to evaluate the concurrent validity and test-retest reliability of mixed reality-based performance tests developed using the Meta Quest 3 platform. Measurement error parameters will also be determined to assess the clinical applicability of these MR-based assessments.
The findings of this study are expected to contribute to the development of safe, standardized, digital, and potentially remote assessment approaches for evaluating functional performance in overweight and obese individuals. Furthermore, the results may strengthen the scientific evidence supporting the use of digital assessment technologies in clinical practice.
調査の概要
研究の種類
観察的
入学 (推定)
119
連絡先と場所
このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。
研究連絡先
- 名前：Mehmet K ALTUNOK, PHD(c) in PT
- 電話番号：+90 5558175133
- メール：mehmetkaan.altunok@selcuk.edu.tr
研究場所
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Selcuklu
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Konya、Selcuklu、トルコ（Türkiye）、42130
- 募集
- Selcuk University, Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation
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コンタクト：
- Mehmet K ALTUNOK, PHD(c) in PT
- 電話番号：+90 5558175133
- メール：mehmetkaan.altunok@selcuk.edu.tr
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参加基準
研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
いいえ
サンプリング方法
非確率サンプル
調査対象母集団
Adults aged 18-65 years with overweight or obesity (BMI ≥25 kg/m²) who are able to ambulate independently and are eligible to participate in conventional and mixed reality-based functional mobility and performance assessments.
説明
Inclusion Criteria:
- Body Mass Index (BMI) ≥ 25 kg/m² (overweight or obesity),
- Ability to ambulate independently,
- Aged between 18 and 65 years,
- Willingness to participate voluntarily in the study and provide written informed consent.
Exclusion Criteria:
- Use of anti-obesity medication,
- Pregnancy,
- Latent autoimmune diabetes in adults (LADA),
- Chronic kidney disease,
- Active or severe infections,
- Liver failure,
- Recent major cardiovascular events,
- Unstable angina,
- Heart failure classified as New York Heart Association (NYHA) Class III-IV,
- Respiratory failure, cardiac arrhythmias, neoplastic diseases, or neurological or musculoskeletal disorders that may limit the safe performance of the tests.
研究計画
このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。
研究はどのように設計されていますか？
デザインの詳細
コホートと介入
グループ/コホート |
介入・治療 |
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Overweight and Obese Individuals
Adults with overweight or obesity (BMI ≥25 kg/m²) who will undergo conventional and mixed reality-based assessments of functional mobility and performance, including the Timed Up and Go Test, 4-Meter Walk Test, and Five-Repetition Sit-to-Stand Test.
Additional assessments of knee extensor muscle strength and handgrip strength will be performed to evaluate convergent validity.
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Participants will perform mixed reality-based adaptations of the Timed Up and Go Test (TUG-MR), 4-Meter Walk Test (4MW-MR), and Five-Repetition Sit-to-Stand Test (5xSTS-MR) developed for the Meta Quest 3 platform.
The mixed reality environment digitally replicates the conventional test setups and provides standardized visual guidance while allowing participants to interact safely with the real environment.
Test outcomes will be automatically recorded by the system and compared with conventional clinical assessments to evaluate validity.
The mixed reality-based tests will be repeated one week later to assess test-retest reliability.
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この研究は何を測定していますか？
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
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Five-Repetition Sit-to-Stand Test - Mixed Reality (5xSTS-MR)
時間枠：Baseline and 1-week follow-up
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Lower extremity functional performance will be assessed using a mixed reality-based adaptation of the Five-Repetition Sit-to-Stand Test.
Test duration will be recorded in seconds, with shorter times indicating better performance.
Validity and reliability will be evaluated through comparison with the conventional Five-Repetition Sit-to-Stand Test and repeated measurements.
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Baseline and 1-week follow-up
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Timed Up and Go Test - Mixed Reality (TUG-MR)
時間枠：Baseline and 1-week follow-up
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Functional mobility will be assessed using a mixed reality-based adaptation of the Timed Up and Go Test.
Test completion time will be recorded in seconds, with shorter times indicating better functional mobility.
Validity will be evaluated by comparison with the conventional Timed Up and Go Test, and reliability will be assessed using repeated measurements performed one week apart.
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Baseline and 1-week follow-up
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4-Meter Walk Test - Mixed Reality (4MW-MR)
時間枠：Baseline and 1-week follow-up
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Walking performance will be assessed using a mixed reality-based adaptation of the 4-Meter Walk Test.
Walking speed will be calculated in meters per second (m/s), with higher values indicating better walking performance.
Validity and reliability will be evaluated through comparison with the conventional 4-Meter Walk Test and repeated measurements.
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Baseline and 1-week follow-up
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
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Participant Satisfaction
時間枠：Baseline
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Participant satisfaction with conventional and mixed reality-based assessments will be evaluated using a 10-point visual analog scale ranging from 1 to 10, with higher scores indicating greater satisfaction.
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Baseline
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Timed Up and Go Test - Conventional
時間枠：Baseline
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The conventional Timed Up and Go Test will be administered to assess functional mobility and will serve as a reference measure for validity analyses.
Test completion time will be recorded in seconds, with shorter times indicating better functional mobility.
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Baseline
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Five-Repetition Sit-to-Stand Test - Conventional
時間枠：Baseline
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The conventional Five-Repetition Sit-to-Stand Test will be used as a reference measure for validity analyses.
Test completion time will be recorded in seconds, with shorter times indicating better lower extremity functional performance.
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Baseline
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Knee Extensor Muscle Strength
時間枠：Baseline
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Knee extensor muscle strength will be measured using a handheld digital dynamometer.
Maximum voluntary contraction values will be recorded, with higher values indicating greater muscle strength.
Outcomes will be analyzed for convergent validity with mixed reality-based test results.
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Baseline
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Handgrip Strength
時間枠：Baseline
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Handgrip strength will be assessed using a hand dynamometer.
The highest value obtained from repeated trials will be recorded, with higher values indicating greater muscle strength.
Outcomes will be analyzed for convergent validity with mixed reality-based test results.
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Baseline
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4-Meter Walk Test - Conventional
時間枠：Baseline
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Walking speed will be assessed using the conventional 4-Meter Walk Test and will serve as a reference measure for validity analyses.
Walking speed will be reported in meters per second (m/s), with higher values indicating better walking performance.
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Baseline
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協力者と研究者
ここでは、この調査に関係する人々や組織を見つけることができます。
スポンサー
捜査官
- スタディチェア：Gülşah ÖZSOY, Assist. Prof. Dr.、Selcuk University, Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation, Konya, Türkiye
- スタディチェア：Zehra KORKUT, Assist. Prof. Dr.、Selcuk University, Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation, Konya, Türkiye
- スタディチェア：İsmail ÖZSOY, Assoc. Prof. Dr.、Selcuk University, Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation, Konya, Türkiye
- スタディチェア：İhsan KODAK, Assist. Prof. Dr.、Kırşehir Ahi Evran University, School of Physical Therapy and Rehabilitation, Kırşehir, Türkiye
- スタディチェア：Yasemin GEDİKLİ ERTÜRK, PhD (c) in PT、Selcuk University, Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation, Konya, Türkiye
- スタディチェア：Selma Ö ÇELİKDELEN, Assist. Prof. Dr.、Konya City Hospital
- スタディチェア：Mehmet A GÜLER, PhD in PT、Selcuk University, Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation, Konya, Türkiye
出版物と役立つリンク
研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。
一般刊行物
- Podsiadlo D, Richardson S. The timed "Up & Go": a test of basic functional mobility for frail elderly persons. J Am Geriatr Soc. 1991 Feb;39(2):142-8. doi: 10.1111/j.1532-5415.1991.tb01616.x.
- Sousa-Santos AR, Amaral TF. Differences in handgrip strength protocols to identify sarcopenia and frailty - a systematic review. BMC Geriatr. 2017 Oct 16;17(1):238. doi: 10.1186/s12877-017-0625-y.
- Cesari M, Kritchevsky SB, Newman AB, Simonsick EM, Harris TB, Penninx BW, Brach JS, Tylavsky FA, Satterfield S, Bauer DC, Rubin SM, Visser M, Pahor M; Health, Aging and Body Composition Study. Added value of physical performance measures in predicting adverse health-related events: results from the Health, Aging And Body Composition Study. J Am Geriatr Soc. 2009 Feb;57(2):251-9. doi: 10.1111/j.1532-5415.2008.02126.x.
- Maggio M, Ceda GP, Ticinesi A, De Vita F, Gelmini G, Costantino C, Meschi T, Kressig RW, Cesari M, Fabi M, Lauretani F. Instrumental and Non-Instrumental Evaluation of 4-Meter Walking Speed in Older Individuals. PLoS One. 2016 Apr 14;11(4):e0153583. doi: 10.1371/journal.pone.0153583. eCollection 2016.
- Greco F, Tarsitano MG, Cosco LF, Quinzi F, Folino K, Spadafora M, Afzal M, Segura-Garcia C, Maurotti S, Pujia R, Pujia A, Buono P, Emerenziani GP. The Effects of Online Home-Based Pilates Combined with Diet on Body Composition in Women Affected by Obesity: A Preliminary Study. Nutrients. 2024 Mar 21;16(6):902. doi: 10.3390/nu16060902.
- Muhla F, Clanche F, Duclos K, Meyer P, Maiaux S, Colnat-Coulbois S, Gauchard GC. Impact of using immersive virtual reality over time and steps in the Timed Up and Go test in elderly people. PLoS One. 2020 Mar 13;15(3):e0229594. doi: 10.1371/journal.pone.0229594. eCollection 2020.
- Saunders S, Reid J, Mehdipour A, D'Amore C, Kuspinar A, Richardson J, Beauchamp M. Virtual Assessment Protocols for Timed-Up-and-Go, 5-Repetition Chair Rise, and 1-Minute Sit-to-Stand Tests in Community-Dwelling Older Adults: Investigating Feasibility, Reliability, and Validity. Arch Phys Med Rehabil. 2025 Jun;106(6):926-933. doi: 10.1016/j.apmr.2024.11.011. Epub 2024 Nov 28.
- Griswold D, Rockwell K, Killa C, Maurer M, Landgraff N, Learman K. Establishing the reliability and concurrent validity of physical performance tests using virtual reality equipment for community-dwelling healthy elders. Disabil Rehabil. 2015;37(12):1097-101. doi: 10.3109/09638288.2014.952451. Epub 2014 Aug 25.
- Chen Y, Guan B, Zhang Y, Lee SC, Liu JY, Li S, Liu M, Zhang X, Ming WK. Acceptability of and Willingness to Use Virtual Reality Exergames for Weight Loss Among Young Adults With Overweight or Obesity in China: Qualitative Study. JMIR Serious Games. 2025 May 1;13:e66998. doi: 10.2196/66998.
研究記録日
これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。
主要日程の研究
研究開始 (実際)
2026年6月10日
一次修了 (推定)
2026年12月30日
研究の完了 (推定)
2027年5月10日
試験登録日
最初に提出
2026年6月12日
QC基準を満たした最初の提出物
2026年6月12日
最初の投稿 (実際)
2026年6月17日
学習記録の更新
投稿された最後の更新 (実際)
2026年6月17日
QC基準を満たした最後の更新が送信されました
2026年6月12日
最終確認日
2026年6月1日
詳しくは
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。