Actively Recruiting

Phase Not Applicable
Age: 40Years - 85Years
All Genders
NCT06272825

Virtual Reality in Patients With Knee Osteoarthritis

Led by Kirsehir Ahi Evran Universitesi · Updated on 2024-08-02

40

Participants Needed

1

Research Sites

33 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

One of the main challenges facing the therapist in the treatment of adhesive capsulitis is to motivate the patient throughout conventional therapy. As noted in a recent review, individuals are more interested in leisure activities rather than performing repetitive tasks during therapy. Virtual reality (VR) is a three-dimensional computer-aided programme built with a system that creates virtual reality movements and generates a high amount of visual and sensory feedback during exercise. As a result, virtual reality (VR) has been used in many medical indications and has been shown to promote adherence to treatment by increasing patient motivation.

CONDITIONS

Official Title

Virtual Reality in Patients With Knee Osteoarthritis

Who Can Participate

Age: 40Years - 85Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of chronic (>3 months) knee osteoarthritis between the ages of 40-85
  • Kellgren and Lawrence Score 65 2 on knee radiograph
  • Visual Analogue Scale result VAS 4-8
Not Eligible

You will not qualify if you...

  • Orthopedic surgery performed on the lower extremity
  • Cognitive dysfunction (Mini Mental Test Score <23)
  • Having received any treatment for knee osteoarthritis in the last 6 months
  • Following any ongoing exercise program (tai chi, pilates, yoga, fitness)
  • History of ligament and ligament injury around the knee

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Kırşehir Ahi Evran University Faculty of Medicine

Kırşehir, City Center, Turkey (Türkiye), 40100

Actively Recruiting

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Research Team

B

Basak Cigdem Karacay, Asst Prof

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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