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Vibration boosts ACL recovery? new study tests quicker muscle healing

NCT ID NCT07555613

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

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Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Aug 21, 2026 · Updated 2 times

Summary

This study tests whether adding gentle vibrations to standard leg exercises helps people regain muscle strength faster after anterior cruciate ligament (ACL) knee surgery. About 62 adults aged 18 to 45 who recently had ACL reconstruction will take part. Half will do rehab exercises with a vibrating device on their thigh, while the other half will do the same exercises without vibration. The goal is to see if the vibration group recovers quadriceps strength and balance more quickly.

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

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

About 62 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Aug 2026

An estimate. Start dates often move.

Expected to finish

Dec 2027

An estimate. End dates often move.

Lead sponsor

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

18 to 45 years

Sex

Anyone

Healthy volunteers

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Men or women who have undergone anterior cruciate ligament reconstruction (using the Kenneth Jones method or a hamstring graft) on the right or left leg * Be between the ages of 18 and 45 * Be enrolled in or eligible for a social security program * Have signed an informed consent form Exclusion Criteria: * Patients who have previously undergone anterior cruciate ligament reconstruction * Patients not currently under care at the Dracy-le-Fort Orthopedic Center * Patients with chronic sensorimotor disorders * Patients who have previously undergone ligament reconstruction on the knee currently being operated on * Patients undergoing surgery more than one year after a cruciate ligament rupture * Pregnant women, women in labor, or breastfeeding women * Individuals subject to legal protection measures (judicial protection, guardianship, or conservatorship) * Individuals deprived of liberty by judicial or administrative order * Individuals receiving psychiatric care * Individuals subject to a period of exclusion for another study * Non-consenting subjects who cannot give consent, or cannot return for scheduled visits as per the protocol

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