MedPath

Home Vs. Physiotherapy Supervised Rehabilitation After ACL Reconstruction

Not Applicable
Completed
Conditions
ACL Reconstruction
Interventions
Procedure: Home-based rehabilitation program
Procedure: Physiotherapy-supervised rehabilitation program
Registration Number
NCT00564837
Lead Sponsor
University of Calgary
Brief 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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
145
Inclusion Criteria
  1. 16 years of age or older
  2. Surgery at least 6 weeks after injury to allow for a return of full range of motion, minimize swelling, and offset strength deficits due to pain/swelling14,28
  3. ACL reconstruction with a bone-patellar tendon-bone autograft
Exclusion Criteria
  1. Previous or concomitant reconstruction of any knee ligament to either knee
  2. Ongoing knee abnormality unrelated to the ACL injury (eg, evidence of changes on radiographs consistent with osteoarthritis)
  3. Professional athletes or workers' compensation patients
  4. Complications during surgery (eg, inadequate graft fixation requiring protocol modification)
  5. Patients without access to local physical therapy services

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Home-basedHome-based rehabilitation programHome-based post-operative rehabilitation program with 4 scheduled physiotherapy sessions over the first 3 post-op months
Physiotherapy supervisedPhysiotherapy-supervised rehabilitation programPhysiotherapy-supervised rehabilitation program including 17 scheduled physiotherapy sessions in the first 3 post-op months
Primary Outcome Measures
NameTimeMethod
Active assisted knee flexion and passive knee extension range of motionpre-op, 6 & 12 weeks post-op
Secondary Outcome Measures
NameTimeMethod
Knee flexion and extension range of motion during gaitpre-op, 6 & 12 wks post-op
Sagittal plane laxity of the kneepre-op, 6 & 12 wks post-op
Isokinetic quadriceps and hamstrings strengthpre-op and 12wks post-op

Trial Locations

Locations (1)

University of Calgary Sport Medicine Centre

🇨🇦

Calgary, Alberta, Canada

© Copyright 2025. All Rights Reserved by MedPath