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

M

Medipol Health Group

Status

Enrolling

Conditions

Foot Diseases

Treatments

Other: Control Group
Other: Video-Based VR Group
Other: VR Biodex Group

Study type

Interventional

Funder types

Other

Identifiers

NCT07260747
E-78097791-020-4737

Details and patient eligibility

About

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

Enrollment

45 estimated patients

Sex

All

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

45 participants in 3 patient groups

VR Biodex Group
Experimental group
Description:
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
Treatment:
Other: VR Biodex Group
Video-Based VR Group
Active Comparator group
Description:
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.
Treatment:
Other: Video-Based VR Group
Control Group
Active Comparator group
Description:
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
Treatment:
Other: Control Group

Trial contacts and locations

1

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Central trial contact

Hazal GENÇ, PhD

Data sourced from clinicaltrials.gov

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