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Vibration shortcut: 5 days of buzz may equal 4 weeks of work

NCT ID NCT07344298

Knowledge-focused Sponsor: Centre Hospitalier Universitaire de Saint Etienne Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
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 Results may not be published yet.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

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looks at whether a short, intense program of local vibration (5 days) can improve leg muscle strength as much as a longer program (4 weeks). 72 healthy adults will try different vibration session lengths (30 or 60 minutes). The goal is to find the most efficient way to use vibration for muscle training and recovery.

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 72 people

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

Started

Mar 2026

Expected to finish

Jan 2028

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

Accepted

You do not need to have the condition being studied to take part.

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 and women, * Aged between 18 and 45, * With a body mass index between 18 and 30 kg/m², * Who have received detailed information about the study and have co-signed the consent form with the investigator, * Who are affiliated with or entitled to social security coverage. Exclusion Criteria: * Subjects with chronic cardiovascular, neuromuscular, bone, metabolic, and/or inflammatory conditions, * Personal history and/or risk factors for thrombosis, * Subjects undergoing antidepressant treatment, * Subjects who have taken corticosteroid treatment in the last 3 months, * Use of neuroactive substances likely to alter corticospinal excitability (hypnotics, antiepileptics, psychotropic drugs, muscle relaxants) during the study period, * History of bone or ligament trauma to the lower limbs within the last 12 months, * Unable to perform the physical efforts required for the study, * Engaging in intense and unusual physical activity, including competitive sports, in the month preceding and during the protocol, * Presence of a skin lesion at the site where the vibrator is to be placed, * Simultaneous participation in another interventional medical trial, * Pregnant and breastfeeding women * Subjects unable to understand the purpose and conditions of the study, unable to give their consent, * Subjects deprived of their liberty or subject to legal protection such as guardianship

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Healthy volonteers

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • CHU de Saint-Etienne

    RECRUITING

    Saint-Etienne, 42055, France

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