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Can gentle vibrations help seniors walk again after a broken hip?

NCT ID NCT07309965

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study looks at whether adding local muscle vibration to standard rehabilitation can help elderly patients (75+) recover strength and mobility after a hip fracture. The vibration is applied to the leg muscles for 30 minutes, five times a week, for four weeks. The main goal is to see if this approach is practical and acceptable for patients and staff, with early signs of whether it improves muscle recovery.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
local muscle vibration therapy
What this could lead to
If it works, this could point toward a simple, drug-free way to speed up recovery and reduce muscle loss after hip fracture in elderly patients.
What could go wrong
This is a very small feasibility study (25 people) with no control group, so it cannot prove effectiveness. The vibration technique may not fit into busy rehab schedules or may not help recovery more than standard care.

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 25 people

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

Started

Nov 2025

Expected to finish

Dec 2026

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

75 years and older

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: * Patients aged 75 or over who have undergone surgery for a fracture of the upper end of the femur * Hospitalised in the SMR department no later than D14 of their operation * Resource Iso Group greater than or equal to 3 on the Aggir scale * Patient capable of consenting who has signed a consent form or patient unable to express consent at the discretion of the principal investigator, informed and not opposed to the study, for whom a trusted person, or if not available, the family, or if not available, a close relative has signed an informed consent within a maximum of 2 days. For patients under guardianship, the guardian's consent will be requested, and for patients under curatorship, the patient will sign the consent in the presence of the curator within a maximum of 2 days as well. * Affiliated to a social security scheme Exclusion Criteria: * Persons deprived of their liberty by a judicial or administrative decision * Individuals with severe psycho-behavioral disorders (major psychiatric or neurocognitive disorders) * Persons admitted to a health or social establishment for purposes other than research * Contraindications to electrical stimulation: * Patient with active devices such as pacemakers, defibrillators, insulin pumps, neurostimulators, etc * Patient with phlebitis or risk of thrombosis * Epileptic patient * Patient with fragile skin or open wounds on the lower limbs * Subject participating in another interventional study with an exclusion period still in progress at pre-inclusion.

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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

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  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.

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  3. A doctor treating you

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Contacts and locations

Locations

  • HOPITAL PIERRE GARRAUD - Service de MEDECINE GERIATRIQUE

    RECRUITING

    Lyon, 69005, France

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