Balance training may help ACL patients walk better
NCT ID NCT07268651
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether adding proprioceptive (balance and coordination) training to standard physical therapy can improve walking and knee function in people who have had ACL reconstruction. Thirty adults aged 18-40 will do either standard rehab or standard rehab plus extra balance exercises for 12 weeks. Researchers will measure walking speed, step length, knee motion, and strength before and after the program.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- proprioceptive training (a type of exercise therapy)
- What this could lead to
- If it works, this could lead to better, more targeted rehab programs that help people walk normally and regain knee function faster after ACL surgery.
- What could go wrong
- This is a small, early-stage study with only 30 participants, so results may not apply to everyone. The training is added 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 30 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Dec 2025
An estimate. Start dates often move.
- Expected to finish
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Apr 2026
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 40 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: * Adults aged 18-40 years who have undergone primary unilateral anterior cruciate ligament reconstruction (ACLR) using an autograft. * At least 3 weeks postoperatively and currently engaged in the early-stage rehabilitation phase following ACLR. * Demonstrate near-full passive knee extension (≤ 5° loss) and at least 90° of passive knee flexion in the operated limb. * Able to walk independently without assistive devices and perform basic functional tasks (e.g., normal walking, single-leg stance). * No prior surgery or major injury to the contralateral knee or other lower limb joints. * No neurological, vestibular, or systemic conditions affecting proprioception, motor control, or physical performance. * Not currently participating in any structured proprioceptive or neuromuscular training programs. * Willing and able to comply with the intervention protocol and follow-up, and able to provide written informed consent. Exclusion Criteria: * History of revision anterior cruciate ligament surgery, bilateral ACLR, or concurrent reconstruction of other knee ligaments (e.g., posterior cruciate ligament, medial collateral ligament, lateral collateral ligament) in the affected knee. * Meniscal repair or other intra-articular procedures that restrict knee range of motion beyond 3 weeks postoperatively. * Diagnosed osteoarthritis, rheumatoid arthritis, or other chronic joint diseases affecting the lower limbs. * Significant injury, surgery, or persistent pain in the contralateral knee, hip, ankle, or spine that could interfere with training or gait. * History or current diagnosis of neurological disorders (e.g., stroke, multiple sclerosis, Parkinson's disease) or vestibular dysfunction. * Any cardiopulmonary or systemic condition that contraindicates structured physical exercise. * Participation in other structured rehabilitation or proprioceptive training programs within the past 3 weeks. * Cognitive impairment or psychiatric conditions that may interfere with understanding instructions or complying with the protocol.
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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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Leshan Vocational College
Leshan, Sichuan, 614000, China
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