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NCT05848622 | RECRUITING | Anterior Cruciate Ligament Injuries

Gait Rehabilitation to Treat FastOA
Sponsor:

University of North Carolina, Chapel Hill

Brief 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.

Condition or disease

Anterior Cruciate Ligament Injuries

Post-traumatic Osteoarthritis

Knee Osteoarthritis

Osteo Arthritis Knee

Knee Injuries

Cartilage, Articular

Gait

Intervention/treatment

Real-time gait biofeedback

Sham real-time gait biofeedback

Phase

NA

Study Type : INTERVENTIONAL
Estimated Enrollment : 70 participants
Masking : DOUBLE
Primary Purpose : PREVENTION
Official Title : Gait Rehabilitation to Treat FastOA
Actual Study Start Date : 2023-06-13
Estimated Primary Completion Date : 2026-05
Estimated Study Completion Date : 2026-05

Information not available for Arms and Intervention/treatment

Ages Eligible for Study: 16 Years to 35 Years
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers:
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 Criteria
  • * A multiple ligament surgery (i.e., PCL)
  • * A lower extremity fracture (i.e., displaced tibial plateau fracture)
  • * Knee osteoarthritis
  • * The participant has a BMI ≥ 36.
Gait Rehabilitation to Treat FastOA

Location Details

NCT05848622

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How to Participate

Want to participate in this study, select a site at your convenience, send yourself email to get contact details and prescreening steps.

Locations

RECRUITING

United States, North Carolina

University of North Carolina at Chapel Hill

Chapel Hill, North Carolina, United States, 27516