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Clinical Trial Summary

This randomized-controlled trial aims to investigate the effect of NMES as an add-on to an exercise program in patients with degenerative meniscus tears.


Clinical Trial Description

To investigate the efficacy of NMES as an add-on to an exercise program, voluntary patients with degenerative meniscus tears, aged between 40 and 65 years, will be randomly divided into two groups: Group 1 (NMES with Exercise) and Group 2 (Exercise). 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 Design


Related Conditions & MeSH terms


NCT number NCT06447129
Study type Interventional
Source Istanbul University - Cerrahpasa (IUC)
Contact Ebru Kaya Mutlu, PT, PhD
Phone 0 266 717 0117
Email fztebrukaya@hotmail.com
Status Recruiting
Phase N/A
Start date June 10, 2024
Completion date October 10, 2024

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