Beep your way to better knee recovery? new study tests metronome exercise after ACL surgery
NCT ID NCT06662955
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether doing a specific knee exercise with a metronome (a device that makes regular beeps) can improve how the thigh muscle works in athletes who recently had ACL reconstruction. 40 participants will do one session of the exercise, with or without the metronome. Researchers will measure muscle signals to see if the metronome helps control the muscle better.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- audible cues (metronome) during exercise
- What this could lead to
- If it works, this could point toward a simple, low-cost way to improve knee muscle recovery after ACL surgery.
- What could go wrong
- This is a very small, early study with only 40 people and a single exercise session. It measures immediate muscle signals, not long-term recovery or function.
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 40 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2024
- Expected to finish
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Dec 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 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Male or female participants who receive primary ACL reconstruction within 2 weeks with or without meniscus repair * No or mild resting pain (Numeric rating scale ≤ 3) * Reconstruction procedures using autograft including hamstrings or bone-patella bone grafts * Age range 18-35 years (33). * BMI of 18.5-25 kg/m² (34). * Tegner activity scale ≥ level 4 Exclusion Criteria: * Non-weight bearing within 2 weeks after the operation (prescription from surgeon) * Hearing problem, such as being unable to hear the metronome sound or being unable to synchronize exercises with the metronome correctly * Limitations in knee extension range caused by joint stiffness evaluated by using passive knee range of motion * Unable to perform active and passive ≥ 30º knee flexion on the operative side * History of serious injury or operation of lower back and lower extremities such as fracture * Lower back or lower extremities pain within 6 months before the study * On the pain killer medication
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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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Faculty of Physical Therapy, Mahidol University
RECRUITINGSalaya, Changwat Nakhon Pathom, 73170, Thailand
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