Comparison of the Effects of Virtual Reality-Based Interventions on Foot Function, Foot Pressure, and Balance in Sedentary Individuals
NCT ID: NCT07260747
Last Updated: 2025-12-03
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
45 participants
INTERVENTIONAL
2025-10-13
2026-05-07
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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VR Biodex Group
This group will participate in a virtual reality-supported rehabilitation program integrated with the Biodex Balance System device. Participants will perform interactive balance and postural stability exercises through this system
VR Biodex Group
This group will participate in a virtual reality-supported rehabilitation program integrated with the Biodex Balance System device.
Video-Based VR Group
Participants in this group will perform balance and foot exercises accompanied by exercise videos containing visual guidance. This intervention aims to provide the virtual reality experience through video-based content.
Video-Based VR Group
: Participants in this group will perform balance and foot exercises accompanied by exercise videos containing visual guidance.
Control Group
This group will follow a traditional home exercise program without any virtual reality intervention. This group will serve as a baseline for comparing the results of the other two groups
Control Group
This group will follow a traditional home exercise program without any virtual reality intervention.
Interventions
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VR Biodex Group
This group will participate in a virtual reality-supported rehabilitation program integrated with the Biodex Balance System device.
Video-Based VR Group
: Participants in this group will perform balance and foot exercises accompanied by exercise videos containing visual guidance.
Control Group
This group will follow a traditional home exercise program without any virtual reality intervention.
Eligibility Criteria
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Inclusion Criteria
* Individuals between the ages of 18-25
* Being a university student
Exclusion Criteria
* Individuals with orthopedic or neurological problems.
* Surgery history
* Cognitive impairment
18 Years
45 Years
ALL
Yes
Sponsors
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Istanbul Medipol University Hospital
OTHER
Responsible Party
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hazal genc
Principal Investigator
Locations
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Bahceşehir University Health Center
Istanbul, , Turkey (Türkiye)
Countries
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Central Contacts
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Facility Contacts
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HAZAL genç, phd
Role: primary
Other Identifiers
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E-78097791-020-4737
Identifier Type: -
Identifier Source: org_study_id
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