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New french tool aims to measure hidden toll on COPD caregivers

NCT ID NCT06652204

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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

Summary

This study tests a French version of a questionnaire that measures the burden on caregivers of people with COPD. Researchers will ask 224 caregivers to fill out the questionnaire along with other surveys to see if it works well. The goal is to give doctors a reliable way to spot and support caregivers who are struggling.

What this could mean

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

What this could lead to
If successful, this study will provide a reliable tool to measure caregiver burden in French-speaking COPD caregivers, helping identify those who need support.
What could go wrong
This is a validation study, not a treatment trial. The questionnaire may not capture all aspects of caregiver burden, and results may not apply to all caregivers.

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.

Participants

About 224 people

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

Started

Oct 2024

Expected to finish

Jun 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.

Who is studied

Informal caregivers of patients with COPD

Ages

18 years and older

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: * Being a caregiver of a relative with COPD (according to the GOLD criteria). * Being 18 years old or older. * The patient under the caregiver's care must be in stable condition (no exacerbations in the previous month). * Being a family member of the patient or living with the patient. * Being able to complete the French questionnaires. * Non-opposition statement provided. NON-INCLUSION CRITERIA * Person under judicial protection (guardianship, curatorship, etc.) * Refusal to participate * The patient under the caregiver's care has experienced an exacerbation in the previous month * The caregiver reports that the patient has cognitive impairments.

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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

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

  1. The places running it

    2 sites. 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

  • Centre hospitalier de Morlaix

    RECRUITING

    Morlaix, 29600, France

  • Chu Brest

    RECRUITING

    Brest, 29609, France

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