Gait Retraining to Reduce Joint Loading, Inflammation, and PTOA Risk
- Conditions
- Anterior Cruciate Ligament Reconstruction
- Registration Number
- NCT03551678
- Lead Sponsor
- VA Palo Alto Health Care System
- Brief Summary
The purpose of this study is to determine changes to knee joint loading, biological markers, and cartilage structure following a novel active feedback gait retraining program in anterior cruciate ligament reconstructed patients.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 45
- age 18-40 years
- history of primary ACLR with or without meniscal repair
- full weight-bearing status
- neutral to varus knee alignment
- plans to remain in the area for at least 8 months.
- Kellgren-Lawrence (KL) radiographic grade > 2
- additional injury or surgery to the involved knee
- BMI >30 kg/m2
- use of walking, orthopedic, or prosthetic assistive device
- pregnancy
- inability to have MRI
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Primary Outcome Measures
Name Time Method Knee Adduction Moment Change from baseline to immediately after 8 weeks of retraining Knee Joint Loading (%Bw\*Ht) will be assessed at baseline and immediately after gait retraining
- Secondary Outcome Measures
Name Time Method Medial knee compartment qMRI Change from baseline to 6 months after retraining Changes to quantitative MRI measures at 6 months after retraining will be correlated with changes to joint loading
Serum inflammatory markers Change from baseline to immediately after 8 weeks of retraining Changes to serum inflammatory markers immediately after the end of training from baseline will be correlated with changes to joint loading
Knee Adduction Moment Change from baseline to 6 months after retraining Knee Joint Loading (%Bw\*Ht)
Trial Locations
- Locations (1)
VA Palo Alto
🇺🇸Palo Alto, California, United States
VA Palo Alto🇺🇸Palo Alto, California, United StatesConstance R Chu, MDContact650-721-7618chucr@stanford.edu