Can visual-guided balance training get ACL patients back on their feet faster?
NCT ID NCT07306221
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether adding visual-guided balance training to standard rehab can improve knee function and walking patterns in people who had ACL reconstruction. 45 patients will be split into two groups: one doing standard rehab plus regular balance exercises, and the other doing standard rehab plus visual-guided balance training. The goal is to see if the visual-guided approach helps patients recover more fully and move more like healthy individuals.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- visual-guided balance training
- What this could lead to
- If it works, this could provide a better rehabilitation method to help people recover knee function and walk more normally after ACL surgery.
- What could go wrong
- This is a small, early-stage trial with only 45 participants, so results may not apply to everyone. The training is an add-on to standard rehab, so any benefit may be modest.
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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About 45 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Nov 2025
- Expected to finish
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Aug 2027
An estimate. End dates often move.
- 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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18 to 45 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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 for patients: 1. Age between 18 and 45 years old; 2. Body Mass Index (BMI) ranging from 18.5 kg/m² to less than 35 kg/m²; 3. First unilateral ACL rupture and reconstruction surgery performed at this hospital; 4. Autologous hamstring tendon transplantation; 5. No or only minor injury to the meniscus, posterior cruciate ligament, medial collateral ligament or lateral collateral ligament; 6. Voluntary participation in this study and signing of informed consent form. Exclusion criteria for patients: 1. Patients who underwent ACL reconstruction more than one year after the injury; 2. Patients with severe injuries to the posterior cruciate ligament, medial collateral ligament or lateral collateral ligament (more than grade I; grade II is partial tear, thickening and tortuosity of the ligament, partial fiber interruption, and swelling of the surrounding soft tissues; grade III is complete rupture). ; Combined with severe meniscus tear; 3. Has a history of previous knee surgery, such as meniscus repair, ligament reconstruction, joint replacement, joint cleaning, etc.; 4. Has other knee joint diseases, such as: knee osteoarthritis, knee joint tumor, rheumatoid arthritis, tuberculosis, knee joint infection or inflammatory diseases, fracture, dislocation or other bone injuries, etc.; 5. Severe heart, lung, brain diseases or liver and kidney dysfunction, and visual and cognitive impairments. Inclusion criteria for the healthy control group 1. Age 18-45 years old; 2. Body Mass Index (BMI) ≥ 18.5 kg/m2 and \< 35 kg/m2; 3. No surgical history, injury history, or chronic joint diseases of the lower extremities; 4. No visual, cognitive impairments or neurological diseases; 5. No trauma or diseases that cause abnormal gait. Exclusion criteria 1\. Poor compliance of the subject; 2. The subject withdraws the informed consent form; 3.The subject requests to terminate the study or is unable to complete all the trials for some reason; 4. The investigator believes that the subject's continued participation in the trial may cause significant adverse effects on their physical condition; 5. The ethics review committee decides to terminate the trial.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Peking University Third Hospital
RECRUITINGBeijing, China
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Other studies related to the condition(s) this trial covers.
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- Which tendon graft helps female athletes recover best after ACL surgery?