Viewing Study NCT06447142



Ignite Creation Date: 2024-06-16 @ 11:50 AM
Last Modification Date: 2024-10-26 @ 3:31 PM
Study NCT ID: NCT06447142
Status: RECRUITING
Last Update Posted: 2024-07-01
First Post: 2024-06-03

Brief Title: The Open Kinetic Chain and Closed Kinetic Chain Strengthening Exercises in Degenerative Meniscus Tears
Sponsor: Istanbul University - Cerrahpasa IUC
Organization: Istanbul University - Cerrahpasa IUC

Study Overview

Official Title: Comparison of the Open Kinetic Chain and Closed Kinetic Chain Strengthening Exercises on Pain Function and Health-related Quality of Life in Degenerative Meniscus Tears
Status: RECRUITING
Status Verified Date: 2024-06
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This randomized-controlled trial aims to compare the effect of open kinetic chain and closed kinetic chain strengthening exercises on pain function and health-related quality of life in degenerative meniscus tears
Detailed Description: Patients with degenerative meniscus tears between the ages of 40 and 65 will be randomly divided into two groups Group 1 open kinetic chain strengthening exercises and Group 2 closed kinetic chain strengthening exercises Interventions will be applied for 16 sessions twice a week for 8 weeks The patients will be assessed at baseline and at the end of the 8-week intervention The pain during activity at rest and at night will be assessed with the Visual Analog Scale VAS Active range of motion will be assessed with a digital goniometer Isometric muscle strength will be measured with a handheld dynamometer The functional status and symptoms will be evaluated by the Knee Injury and Osteoarthritis Outcome Score KOOS and Lysholm Knee Scoring Scale Health-related quality of life will be assessed with the Short Form-12 SF-12

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None