Home Vs. Physiotherapy Supervised Rehabilitation After ACL Reconstruction

Status Completed

Clinical Trial Summary

This study was designed to determine whether or not there were any differences in knee range of motion, both statically and during gait, sagittal plane knee laxity, and quadriceps and hamstrings strength in patients three months post-ACL reconstruction with a bone-patellar tendon-bone autograft based on their performance of a primarily home based rehabilitation program or a standard physiotherapy-supervised program.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

ACL Reconstruction

Clinical Trial Details

NCT number	NCT00564837
Study type	Interventional
Source	University of Calgary
Contact
Status	Completed
Phase	N/A
Start date	September 1999
Completion date	February 2001

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