The purpose of this study is to report the feasibility and determine the initial effects of 18 sessions of real-time gait biofeedback delivered over a 6-week period on retention and transfer of normalized gait biomechanics and improvements in indicators of early post-traumatic osteoarthritis development in those with an anterior cruciate ligament reconstruction (ACLR) at 6 and 8-week posttests.
Age range
18 Years – 35 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Number of participants recruited using different recruitment modes
Timeframe: Baseline (pre-intervention)
The frequency of participant recruitment using different recruitment modes
Timeframe: Baseline (pre-intervention)
Percentage of participants who were successfully enrolled
Timeframe: Baseline (pre-intervention)
Percentage of participants retained
Timeframe: After week 4 and after week 8
Reasons for refusal to enroll
Timeframe: Baseline (pre-intervention)
Number of subjects who adhered to the intervention
Timeframe: About 2 months