NCT07260747 Comparison of the Effects of Virtual Reality-Based Interventions on Foot Function, Foot Pressure, and Balance in Sedentary Individuals
| NCT ID | NCT07260747 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Istanbul Medipol University Hospital |
| Condition | Foot Diseases |
| Study Type | INTERVENTIONAL |
| Enrollment | 45 participants |
| Start Date | 2025-10-13 |
| Primary Completion | 2025-11-15 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 45 participants in total. It began in 2025-10-13 with a primary completion date of 2025-11-15.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
Comparison of the Effects of Virtual Reality-Based Interventions on Foot Function, Foot Pressure, and Balance in Sedentary Individuals
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
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07260747 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 45 Years, studying Foot Diseases. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07260747 currently recruiting?
Yes, NCT07260747 is actively recruiting participants. Contact the research team at hazaloksuz@gmail.com for enrollment information.
Where is the NCT07260747 trial being conducted?
This trial is being conducted at Istanbul, Turkey (Türkiye).
Who is sponsoring the NCT07260747 clinical trial?
NCT07260747 is sponsored by Istanbul Medipol University Hospital. The trial plans to enroll 45 participants.