Recruiting NCT07260747
Comparison of the Effects of Virtual Reality-Based Interventions on Foot Function, Foot Pressure, and Balance in Sedentary Individuals
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: VR Biodex Group, Video-Based VR Group, Control Group.
- Who it may be relevant to
- Registry conditions: Foot Diseases. Basic parameters: 18 years — 45 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Turkey (Türkiye)
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
Comparison of the Effects of Virtual Reality-Based Interventions on Foot Function, Foot Pressure, and Balance in Sedentary Individuals
Interventions
- Other VR Biodex Group
This group will participate in a virtual reality-supported rehabilitation program integrated with the Biodex Balance System device. - Other Video-Based VR Group
: Participants in this group will perform balance and foot exercises accompanied by exercise videos containing visual guidance. - Other Control Group
This group will follow a traditional home exercise program without any virtual reality intervention.
Primary outcome measures
- Foot Function Assessment [Time frame: 6 weeks]
- Foot Pressure Assessment - Maximum Plantar Pressure [Time frame: 6 weeks]
- Foot Pressure Assessment - Contact Area [Time frame: 6 weeks]
- Foot Pressure Assessment - Center of Pressure (COP) [Time frame: 6 weeks]
- Balance Performance Assessment [Time frame: 6 weeks]
- Physical Activity Level Assessment [Time frame: 6 weeks]
Eligibility criteria
Inclusion criteria
- Sedentary Individual
- Individuals between the ages of 18-25
- Being a university student
Exclusion criteria
- Athletes
- Individuals with orthopedic or neurological problems.
- Surgery history
- Cognitive impairment
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Treatment
Study locations
Turkey (Türkiye) · 1 center
- Bahceşehir University Health Center — Istanbul
Identifiers
NCT: NCT07260747 · E-78097791-020-4737