Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Cure My Disease

Don't miss your cure!

 Log in / Sign up

Dignity in design: new garment aims to ease dementia incontinence care

NCT ID NCT05649839

Symptom relief Sponsor: Centre Hospitalier Universitaire, Amiens Source: ClinicalTrials.gov ↗

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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 26, 2026 · Updated 1 time

Summary

This study tests a specially designed garment for elderly dementia patients who have incontinence and often remove their protective pads. The goal is to see if a more dignified, comfortable garment can improve satisfaction for patients and caregivers. Forty participants will be randomly assigned to wear the new garment or standard care, and their satisfaction will be measured.

What this could mean

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

Active substance
specially designed garment
What this could lead to
If successful, this could provide a more dignified and effective way to manage incontinence in dementia patients, reducing the need for restraints or sedatives.
What could go wrong
This is a small, early-stage trial with only 40 participants, and the garment may not be acceptable to all patients or caregivers. The main outcome is satisfaction, not clinical improvement.

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

40 people

The number who actually took part.

Started

Dec 2022

Expected to finish

Jan 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

18 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 hospitalized in a cognitive-behavioral unit or long-term care or residents of the EHPAD at the St-Victor center - CHU Amiens-Picardie, * patients with behavioral and sphincter disorders justifying the prescription of a romper. * signature of a consent exclusion criteria Exclusion Criteria: * No next of kin * Patients in terminal palliative care * Patients whose morphology does not allow the use of prototypes (no adapted size)

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Adapted garment prototype are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

Conditions

The condition(s) this trial relates to.

Alzheimer disease dementia Problem Behavior

As listed by the trial registrant

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

Adapted garment prototype Dementia Elderly Problem behavior Sphincter disorders

Contacts and locations

Locations

  • Centre Hospitalier Universitaire d'Amiens

    Amiens, Picardie, 80000, France

More trials for these conditions

Other studies related to the condition(s) this trial covers.