Effects of Contralateral Strength Training on Postoperative Strength Deficits in the Immobilized Lower Extremity

Not Applicable

Recruiting

• Conditions: Meniscus; Detachment, Current Injury

• Registration Number: NCT03650374
• Lead Sponsor: NYU Langone Health

Brief Summary

This is a prospective, randomized controlled trial that will enroll patients undergoing unilateral meniscal root repair or meniscus transplant. The objective of this study is to determine if immediate postoperative strength training of the contralateral (non-surgical) lower extremity reduces postoperative loss of strength in an immobilized lower extremity.

After the completion of surgery, patients will be randomized to either the experimental treatment (Group 1) or control group (Group II)for postoperative rehabilitation.

Detailed Description

Group I will receive knee flexion and extension strength training exercises for the contralateral (non-operative) lower extremity in addition to standard of care postoperative rehabilitation. The experimental strength training will be performed with moderate resistance and will require moderate effort. Exercises will include unilateral leg presses, lunges, step ups, and step downs. These exercises are performed as standard of care but are not typically introduced into the physical therapy regimen until 10-12 weeks postoperatively. In the experimental group, these exercises will be introduced starting with the first postoperative physical therapy session, but only for the contralateral (non-operative) leg.

Study Timeline

• Study First Submitted: 2018-08-27
• Study First Submitted QC: 2018-08-27
• Study First Posted: 2018-08-28
• Study Start: 2021-09-01
• Status Verified: 2025-04
• Last Update Submitted: 2025-04-24
• Last Update Posted: 2025-04-25
• Primary Completion: 2025-12-01
• Study Completion: 2025-12-01

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

• Patient is indicated for meniscal root repair
• Patient is indicated for meniscus transplant
• Patient is at least 18 years of age
• Patient is expected to survive at least 1 year beyond surgery
• Patient has intact lower extremities bilaterally
• Patient is willing to participate by complying with pre-and post-operative visit requirements
• Patient is willing and able to review and sign a study informed consent form

Exclusion Criteria

• Lower extremity musculoskeletal defects
• Systemic neuromuscular disorders
• Failure to complete pre-operative BIDOEX strength assessment
• Failure to complete pre-operative self-assessment score intake forms

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
KOOS	6 Weeks, 3 Months, 6 Months	A patient-reported outcome measurement instrument, developed to assess the patient's opinion about their knee and associated problems.

Trial Locations

Locations (1)

New York University School of Medicine; 🇺🇸 New York, New York, United States