Gait Rehabilitation to Treat FastOA
Recruiting · NCT05848622 · Interventional (participants receive a specific treatment) · Lead sponsor: University of North Carolina, Chapel Hill
View the official record on ClinicalTrials.gov →Interventions studied
Real-time gait biofeedbackSham real-time gait biofeedback
What this trial is about
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.
Who can take part
Age range
16 Years to 35 Years
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
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
Where it is running
1 location listed across 1 US state.
- University of North Carolina at Chapel Hill - Chapel Hill, North Carolina, United States