Video Exercise Mobile Application for People With Knee Osteoarthritis

Osteoarthritis, Knee Clinical Trial

Official title:

Development and Investigation of the Effectiveness of Video Exercise Mobile Application for People With Knee Osteoarthritis

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT06422910
• Other study ID #: Tubitak diz OA
• Status: Completed
• Phase: N/A
• Start date: May 2, 2023
• Est. completion date: May 15, 2024

Study information

• Verified date: May 2024
• Source: Mugla Sitki Koçman University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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

Recruitment information / eligibility

• Status: Completed
• Enrollment: 52
• Est. completion date: May 15, 2024
• Est. primary completion date: April 30, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

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

Related Conditions & MeSH terms

• Osteoarthritis
• Osteoarthritis, Knee
• Telerehabilitation

Intervention

Other:
• Telerehabilitation
Home exercises will be delivered through a video mobile application. In this application, exercises for knee osteoarthritis will be presented according to their types (stretching, strengthening, etc.). Videos deemed appropriate by the physiotherapist will be added to the exercise prescription and sent to the patients via message. Patients will have the opportunity to remotely access their own exercise prescription with visual, auditory and written commands. Translated with DeepL.com (free version)

Locations

Country	Name	City	State
Turkey	Fethiye State Hospital	Mugla	Fethiye

Sponsors (2)

Lead Sponsor	Collaborator
Fatih Ozden	The Scientific and Technological Research Council of Turkey

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Visual Analog Scale (VAS)	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).	Change from Baseline VAS at 8 weeks
Primary	The Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)	WOMAC consists of 3 main headings: pain intensity, stiffness and physical function. The total score ranges from 0 (no disability) to 96 (complete disability).	Change from Baseline WOMAC at 8 weeks
Primary	Satisfaction and expectation assessment	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.	Change from Baseline Satisfaction and expectation assessment at 8 weeks