Video Exercise Mobile Application for People With Knee Osteoarthritis

Not Applicable

Completed

• Conditions: Osteoarthritis, Knee; Telerehabilitation

• Registration Number: NCT06422910
• Lead Sponsor: Fatih Ozden

Brief Summary

The aim of our study is to realize an exercise training and follow-up system that individuals with knee OA can easily adapt.

Detailed Description

Not available

Study Timeline

• Study Start: 2023-05-02
• Primary Completion: 2024-04-30
• Status Verified: 2024-05
• Study Completion: 2024-05-15
• Study First Submitted: 2024-05-15
• Study First Submitted QC: 2024-05-15
• Last Update Submitted: 2024-05-15
• Study First Posted: 2024-05-21
• Last Update Posted: 2024-05-21

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 52

Inclusion Criteria

• Diagnosis of primary knee osteoarthritis (OA) according to the American College of Rheumatology (ACR) criteria
• Be qualified to use the mobile application and agree to use the application

Exclusion Criteria

• Individuals with poor cognitive function or inadequate reading skills
• Individuals with neurological disorders that may affect mobility skills
• Individuals who have undergone knee joint surgery and individuals with traumatic injuries

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Satisfaction and expectation assessment	Change from Baseline Satisfaction and expectation assessment at 8 weeks	On a 0 cm straight line or numeric scale, the patient will be asked to mark their pre-treatment expectation and post-treatment satisfaction level. 0 will represent the lowest expectation and satisfaction and 10 the highest expectation or satisfaction.
Visual Analog Scale (VAS)	Change from Baseline VAS at 8 weeks	On a 0 cm straight line or numeric scale, the patient is asked to mark the pain they feel (0: no pain, 10: excruciating pain).
The Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)	Change from Baseline WOMAC at 8 weeks	WOMAC consists of 3 main headings: pain intensity, stiffness and physical function. The total score ranges from 0 (no disability) to 96 (complete disability).

Trial Locations

Locations (1)

Fethiye State Hospital; 🇹🇷 Muğla, Fethiye, Turkey