Back to Trials
NCT05848622NARecruiting

Gait Rehabilitation to Treat FastOA

University of North Carolina, Chapel Hill

Start Date

6/13/2023

Completion Date

6/1/2027

Summary

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.

Eligibility Criteria

Age Range: 16 years to 35 years

Inclusion Criteria: * 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) Exclusion Criteria: * A multiple ligament surgery (i.e., PCL) * A lower extremity fracture (i.e., displaced tibial plateau fracture) * Knee osteoarthritis

Interventions

BEHAVIORAL

Real-time gait biofeedback

BEHAVIORAL

Sham real-time gait biofeedback

Interested in This Trial?

Contact the trial locations directly using the information below to learn more about enrollment.

Expressing interest lets you review the study and consent before we connect you with the research site.

Conditions

Anterior Cruciate Ligament InjuriesPost-traumatic OsteoarthritisKnee OsteoarthritisOsteo Arthritis KneeKnee InjuriesCartilage, ArticularGait

Locations

University of North Carolina at Chapel Hill

Chapel Hill, North Carolina 27516

United States