Gait Rehabilitation to Treat FastOA

Recruiting N/A Interventional Study
Anterior Cruciate Ligament Injuries Post-traumatic Osteoarthritis Knee Osteoarthritis Osteo Arthritis Knee Knee Injuries Cartilage, Articular Gait
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
16 – 35
Sex
Any
Study type
Interventional
Purpose
Prevention
Participants needed
70 (estimated)
Sponsor
University of North Carolina, Chapel Hill · Other
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About This Trial

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.

Trial Locations
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Eligibility Criteria
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 Cr…
Contacts

Natalia Favoreto, MS

9199622025

favoreto@med.unc.edu

CONTACT

Brian Pietrosimone, PhD

19199623617

pietrosi@email.unc.edu

CONTACT