Comparison of the Effects of Virtual Reality-Based Interventions on Foot Function, Foot Pressure, and Balance in Sedentary Individuals

ConditionFoot Diseases
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-45
SponsorIstanbul Medipol University Hospital

About this trial

Comparison of the Effects of Virtual Reality-Based Interventions on Foot Function, Foot Pressure, and Balance in Sedentary Individuals

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Sedentary Individual

Individuals between the ages of 18-25

Being a university student

Disqualifiers

Athletes

Individuals with orthopedic or neurological problems.

Surgery history

Cognitive impairment

Trial design

Design model

Parallel

Treatments tested in this trial

  • VR Biodex Group

    Other intervention

    This group will participate in a virtual reality-supported rehabilitation program integrated with the Biodex Balance System device.

  • Video-Based VR Group

    Other intervention

    : Participants in this group will perform balance and foot exercises accompanied by exercise videos containing visual guidance.

  • Control Group

    Other intervention

    This group will follow a traditional home exercise program without any virtual reality intervention.

Treatment groups

45 Participants
are divided into 3 treatment groups
Group A: VR Biodex GroupExperimental treatment 1 intervention
Group B: Video-Based VR GroupActive comparator 1 intervention
Group C: Control GroupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Foot Function Assessment

Foot pain, disability, and activity limitation will be assessed using the Foot Function Index (FFI), a validated 23-item questionnaire. The total FFI score ranges from 0 to 100, with higher scores indicating worse foot function (greater pain, disability, and activity limitation).

Time frame
6 weeks
2

Foot Pressure Assessment - Maximum Plantar Pressure

Plantar pressure during standing and walking will be assessed using a pedobarographic measurement system. Maximum plantar pressure will be recorded, with higher values indicating greater localized loading on the foot.

Time frame
6 weeks
3

Foot Pressure Assessment - Contact Area

The pedobarographic system will measure the total plantar contact area during standing and walking. Larger contact area values indicate greater surface area participation in load distribution.

Time frame
6 weeks
4

Foot Pressure Assessment - Center of Pressure (COP)

The pedobarographic system will measure center of pressure displacement during standing and walking. COP path characteristics provide objective indicators of stability and gait mechanics; greater displacement typically indicates reduced postural control.

Time frame
6 weeks

Secondary outcomes

Other outcomes

Sponsors and contacts

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