Squat biofeedback may stop knee arthritis after ACL injury
NCT ID NCT05363683
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether a visual biofeedback program during squats can improve knee loading and prevent osteoarthritis after ACL reconstruction. 34 participants were assigned to either standard physical therapy or standard therapy plus real-time visual feedback on a screen during squats. The goal was to see if the feedback could help restore normal knee movement and reduce early signs of cartilage damage seen on MRI.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Squat biofeedback (visual feedback during squats using force plates)
- What this could lead to
- If successful, this could lead to a new rehabilitation method to prevent knee osteoarthritis after ACL injury.
- What could go wrong
- This is a small, early-stage study with only 34 participants. The biofeedback may not produce lasting changes or prevent osteoarthritis in the long term.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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34 people
The number who actually took part.
- Started
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Nov 2021
- Finished
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Jun 2024
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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13 to 35 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Acute anterior cruciate ligament (ACL) injury in the past 6 months * ACL reconstruction in the past month or have a planned ACL reconstruction Exclusion Criteria: * Previous knee injury or surgery (contralateral knee) * Body mass index (BMI) over 35 kg/m2 * Concomitant posterior cruciate ligament reconstruction or cartilage procedure that includes extended weight bearing restrictions and/or changes to cartilage structure * Current or planned pregnancy during study duratuiom
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
University of Nebraska Medical Center
Omaha, Nebraska, 68198, United States
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