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Clinical Trials/NCT05266365
NCT05266365
Active, not recruiting
Not Applicable

Investigation of the Efficacy of Video-Based Exercise Programs in Degenerative Meniscus Tears

Istanbul University - Cerrahpasa1 site in 1 country81 target enrollmentApril 1, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Degenerative Disease
Sponsor
Istanbul University - Cerrahpasa
Enrollment
81
Locations
1
Primary Endpoint
Knee Injury and Osteoarthritis Outcome Score (KOOS)
Status
Active, not recruiting
Last Updated
5 months ago

Overview

Brief Summary

This randomized controlled trial aims to investigate the efficacy of the video-based exercise programs in patients with degenerative meniscus tears.

Detailed Description

To investigate the efficacy of video-based exercise programs, voluntary patients with degenerative meniscus tears aged 40-65 years will be randomly assigned to three groups: the hybrid exercise group (HEG), the video-based exercise (VBE) group, and the standard exercise (SE) group. Interventions will be delivered over 16 sessions (twice a week for 8 weeks). The patients will be assessed at baseline and at the end of the 8-week intervention. Pain during activity, at rest, and at night will be assessed using the Visual Analog Scale (VAS). Active range of motion will be evaluated using a digital goniometer. Isometric muscle strength will be measured with a handheld dynamometer. The Knee Injury and Osteoarthritis Outcome Score (KOOS) will evaluate functional status and symptoms. The Western Ontario Meniscal Evaluation Tool (WOMET) will assess health-related quality of life. Adherence to the exercise program and the Global Rating of Change Scale will be evaluated.

Registry
clinicaltrials.gov
Start Date
April 1, 2022
End Date
January 5, 2026
Last Updated
5 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Istanbul University - Cerrahpasa
Responsible Party
Principal Investigator
Principal Investigator

Tansu Birinci

Principal Investigator

Istanbul University - Cerrahpasa

Eligibility Criteria

Inclusion Criteria

  • Being aged between 40 and 65 years
  • Having the degenerative meniscus tear in at least one knee
  • Having body mass index in the range of 18-30 kg/m2
  • Feeling the pain that lasts for at least 2 months
  • Having grade 1 or grade 2 degenerative meniscal tear diagnosed by an orthopedic specialist according to the MRI results
  • Having the activity level is between 1 and 5 according to the Tegner Activity Scale
  • Having access to the internet via a computer or smartphone
  • Having the ability to read and write Turkish

Exclusion Criteria

  • Having undergone arthroscopic partial meniscectomy surgery due to degenerative meniscal tear
  • Participating in a physiotherapy program for degenerative meniscal tear in the last 12 weeks
  • Have received steroid injections in the last 6 months
  • Accompanying conditions such as injury to the surrounding ligaments, congenital anomaly in the affected knee, coxarthrosis and spinal stenosis
  • Presence of any systemic disorder that may affect assessment parameters
  • Failure to cooperate with assessments
  • Any vision or hearing problem that would prevent them from adapting to the assessment

Outcomes

Primary Outcomes

Knee Injury and Osteoarthritis Outcome Score (KOOS)

Time Frame: Baseline

Short-term and long-term symptoms and function will be assessed with the Knee injury and Osteoarthritis Outcome Score (KOOS) that is developed as an extension of the WOMAC Osteoarthritis Index. The score is a percentage score from 0 to 100, 0 representing extreme problems and 100 representing no problems.

Secondary Outcomes

  • Active Range of Motion(At the end of 8-week intervention)
  • Western Ontario Meniscal Evaluation Tool (WOMET)(At the end of the 8-week intervention)
  • Visual Analogue Scale (VAS)(After 8-week intervention)
  • Muscle Strength(At the end of the 8-week intervention)
  • Knee Injury and Osteoarthritis Outcome Score (KOOS)(At the end of 8-week intervention)

Study Sites (1)

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