Skip to main content
OpenTrials
Recruiting

NCT Number: NCT07260747

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

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

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year–45 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Bahceşehir University Health Center

Istanbul, 34070, Turkey (Türkiye)

Location status: Recruiting

Location contact

HAZAL genç, phd

CONTACT

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

VR Biodex Group

Other

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

Video-Based VR Group

Other

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

Control Group

Other

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

Primary outcomes

  1. Foot Function Assessment

    Time frame: 6 weeks

    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).

  2. Foot Pressure Assessment - Maximum Plantar Pressure

    Time frame: 6 weeks

    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.

  3. Foot Pressure Assessment - Contact Area

    Time frame: 6 weeks

    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.

  4. Foot Pressure Assessment - Center of Pressure (COP)

    Time frame: 6 weeks

    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.

  5. Balance Performance Assessment

    Time frame: 6 weeks

    Static and dynamic balance performance will be assessed using the Biodex Balance System. The system provides balance scores ranging from 0 to 12, where lower scores indicate better balance performance.

  6. Physical Activity Level Assessment

    Time frame: 6 weeks

    Physical activity levels will be assessed using the International Physical Activity Questionnaire (IPAQ) - Short Form. Weekly metabolic equivalent of task (MET-minutes/week) will be calculated to classify physical activity as low, moderate, or high. Higher MET-minutes/week indicate higher physical activity levels.

Study contacts

Contact information is provided by the study sponsor or research team.

Hazal GENÇ, PhD

CONTACT

[email protected]

05413204291

Sponsors and collaborators

Lead sponsor

Istanbul Medipol University Hospital

Other

Registry information

Important dates

Study start
2025
Primary completion
2025
Study completion
2026
First posted
Dec 3, 2025
Registry last updated
Dec 3, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.