RecruitingAnterior Cruciate Ligament InjuriesPost-traumatic OsteoarthritisKnee Osteoarthritis
Gait Rehabilitation to Treat FastOA
Eligible age
16–35 yrs
Accepts
All genders
Locations
1 state
Healthy volunteers
No
See if you qualify for this study
Answer a few quick questions about your location and health. Takes about a minute.
About this study
The purpose of this study is to determine the effects of real-time gait biofeedback delivered over a 6-week period on early markers of FastOA and conduct 6-week and 6-month follow-up assessments in anterior cruciate ligament reconstructed patients.
Sponsor: University of North Carolina, Chapel Hill
You may qualify if…
- ✓ Have completed all other formal physical therapy
- ✓ Are between the ages of 16 and 35
- ✓ Underwent an anterior cruciate ligament reconstruction (ACLR) between 6 and 60 months prior to enrollment
- ✓ Demonstrate underloading during gait (vGRF- impact peak \<1.12 x BW)
You may not qualify if…
- ✕ A multiple ligament surgery (i.e., PCL)
- ✕ A lower extremity fracture (i.e., displaced tibial plateau fracture)
- ✕ Knee osteoarthritis
Where it's recruiting
North Carolina
Chapel Hill
Source: ClinicalTrials.gov · NCT05848622 · last updated 2026-05-28