Type 2 Diabetes (T2D) Clinical Trials

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Validity and Reliability of the Mixed Reality Adaptation of the 6-Minute Walk, Timed Up and Go, and Five-Repetition Sit-to-Stand Tests in Individuals With Type 2 Diabetes Mellitus

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
SUMMARY

Type 2 Diabetes Mellitus (T2DM) is a multifaceted metabolic disease associated not only with impaired glycemic control but also with reductions in muscle strength, balance, functional mobility, and walking performance. Individuals with T2DM may experience impairments in lower extremity function, postural control, and overall functional performance, which can negatively affect activities of daily living and quality of life. Therefore, the assessment of functional performance using reliable and valid methods is important for clinical monitoring and rehabilitation planning. The 6-Minute Walk Test (6MWT), Timed Up and Go Test (TUG), and Five-Repetition Sit-to-Stand Test (5xSTS) are widely used clinical assessments for evaluating walking capacity, functional mobility, lower extremity function, and physical performance in individuals with T2DM. Previous studies have demonstrated that these tests provide reliable and clinically meaningful measurements in this population. In recent years, virtual and mixed reality technologies have provided opportunities to conduct assessments in a more objective, standardized, and user-friendly manner. These technologies also offer important advantages, including real-time data collection, enhanced user interaction, and potential integration into future remote assessment applications. However, evidence regarding the measurement properties of mixed reality-based adaptations of commonly used functional performance tests in individuals with T2DM remains limited. The aim of this study is to evaluate the validity and reliability of mixed reality-based adaptations of the 6-Minute Walk Test, Timed Up and Go Test, and Five-Repetition Sit-to-Stand Test developed using the Meta Quest 3 platform. In addition, convergent validity will be examined by investigating the relationships between outcomes obtained from the mixed reality-based assessments and measures of knee extensor muscle strength and handgrip strength. The findings of this study are expected to contribute to the development of innovative, safe, standardized, and digital approaches for assessing functional performance in individuals with Type 2 Diabetes Mellitus. Furthermore, the results may provide a scientific foundation for future digital health applications and remote assessment strategies.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
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• Diagnosed with Type 2 Diabetes Mellitus by a physician,

• Aged between 18 and 65 years,

• Ability to ambulate independently without the use of an assistive device,

• No participation in a structured exercise program within the previous 6 months,

• Cognitive ability sufficient to understand and follow test instructions,

• Visual, auditory, and vestibular functions sufficient to tolerate mixed reality applications,

• Ability to read, understand, and follow instructions in Turkish,

• Willingness to participate voluntarily in the study and provision of written informed consent.

Locations
Other Locations
Turkey
Selcuk University, Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation
RECRUITING
Konya
Contact Information
Primary
Mehmet K ALTUNOK, PHD(c) in PT
mehmetkaan.altunok@selcuk.edu.tr
5558175133
Time Frame
Start Date: 2026-06-10
Estimated Completion Date: 2027-05-10
Participants
Target number of participants: 75
Treatments
Individuals with Type 2 Diabetes Mellitus
Adults aged 18-65 years diagnosed with Type 2 Diabetes Mellitus who will undergo conventional and mixed reality-based assessments of functional performance, including the 6-Minute Walk Test, Timed Up and Go 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.
Related Therapeutic Areas
Sponsors
Leads: Selcuk University

This content was sourced from clinicaltrials.gov