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



Status:Recruiting
Healthy:No
Age Range:18 - 90
Updated:10/19/2018
Start Date:August 9, 2018
End Date:June 2019
Contact:Sam Baron
Email:Sam.Baron@nyulangone.org
Phone:646 501 7223

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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.

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.

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
We found this trial at
1
site
550 1st Ave
New York, New York 10016
(212) 263-7300
Principal Investigator: Guillem Gonzalez-Lomas, MD
Phone: 646-501-7223
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