Gait Rehabilitation to Treat FastOA

Recruiting now · Not applicable · Has a placebo group

Conditions studied: Anterior Cruciate Ligament Injuries, Post-traumatic Osteoarthritis, Knee Osteoarthritis, Osteo Arthritis Knee, Knee Injuries, Cartilage, Articular, Gait

In brief

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.

Key facts

Study ID

NCT05848622

Run by

University of North Carolina, Chapel Hill

People needed

70

Starts

2023-06-13

Expected to finish

2027-06-01

Last updated by the study team

2026-06-25

Who can join

Age: 16 and older, up to 35. Sex: any. Healthy volunteers: not accepted.

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 is running

• University of North Carolina at Chapel Hill — Chapel Hill, North Carolina, United States (enrolling)

Full record on ClinicalTrials.gov

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