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New wheelchair brake could make slopes safer

NCT ID NCT06524128

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 tested a new braking system called Dreeft® for manual wheelchairs. The goal was to see if it helps users feel more satisfied and perform daily tasks more easily. 24 adults with motor disabilities who use a manual wheelchair took part. The study measured changes in satisfaction and performance with daily activities.

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

24 people

The number who actually took part.

Started

Jul 2024

Finished

May 2025

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 63 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: * Male or female aged ≥ 18 years and \< to 64 years. * Participants having signed the written consent form to participate in the study after free and informed information. * Wheelchair user for more than one year. * Participants affiliated to a social security scheme (beneficiary or beneficiary's beneficiary) excluding AME. * Living at home. * Have a motor disability, whatever its origin, and use a manual wheelchair independently as their main mobility tool, with or without propulsion assistance. * Who propel their manual wheelchair with both upper limbs. * Using a personal manual wheelchair compatible with Dreeft® wheels. * Able to mount/dismount the wheels, or a third party to assist with wheel changes. * Referred by the person's referring physician or occupational therapist on clinical indication for the device. Exclusion Criteria: * Participant deprived of liberty (by judicial or administrative decision). * Participant of legal age under legal protection or unable to express consent. * Participation in another ongoing clinical trial. * Pregnant or breastfeeding women or women of childbearing age without contraception. * Lack of proficiency in spoken and written French. * Unstable health condition. * Mentally or linguistically incapable of understanding the instructions for taking the research tests. * User unable to propel himself/herself independently in a manual wheelchair, hemiplegic user. * Body weight \> 120 kg

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As listed by the trial registrant

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

Contacts and locations

Locations

  • Centre de ressources et d'innovation mobilité handicap (CEREMH)

    Vélizy-Villacoublay, 78140, France

  • Centre de rééducation et de réadaptation fonctionnelles de Kerpape

    Ploemeur, 56270, France