Home Vs. Physiotherapy Supervised Rehabilitation After ACL Reconstruction
Not Applicable
Completed
- Conditions
- ACL Reconstruction
- Interventions
- Procedure: Home-based rehabilitation programProcedure: 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
- 16 years of age or older
- 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
- ACL reconstruction with a bone-patellar tendon-bone autograft
Exclusion Criteria
- Previous or concomitant reconstruction of any knee ligament to either knee
- Ongoing knee abnormality unrelated to the ACL injury (eg, evidence of changes on radiographs consistent with osteoarthritis)
- Professional athletes or workers' compensation patients
- Complications during surgery (eg, inadequate graft fixation requiring protocol modification)
- Patients without access to local physical therapy services
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Home-based Home-based rehabilitation program Home-based post-operative rehabilitation program with 4 scheduled physiotherapy sessions over the first 3 post-op months Physiotherapy supervised Physiotherapy-supervised rehabilitation program Physiotherapy-supervised rehabilitation program including 17 scheduled physiotherapy sessions in the first 3 post-op months
- Primary Outcome Measures
Name Time Method Active assisted knee flexion and passive knee extension range of motion pre-op, 6 & 12 weeks post-op
- Secondary Outcome Measures
Name Time Method Knee flexion and extension range of motion during gait pre-op, 6 & 12 wks post-op Sagittal plane laxity of the knee pre-op, 6 & 12 wks post-op Isokinetic quadriceps and hamstrings strength pre-op and 12wks post-op
Trial Locations
- Locations (1)
University of Calgary Sport Medicine Centre
🇨🇦Calgary, Alberta, Canada