Clinical trial Recruiting at 2 sites Observational Ages 18 and up

French QASCI questionnaire for caregivers of people with COPD

Official title: Validation of the French Version of the Informal Caregiver Burden Assessment Questionnaire (QASCI) in Caregivers of Patients With COPD (VALQASCI)

Run by University Hospital, Brest · NCT06652204 · Data updated 2026-11-12

This project will test the French version of the QASCI questionnaire to see if it works well for caregivers of people with COPD.

More Caregiver trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment224 (estimated)
SponsorUniversity Hospital, Brest
Academic / other
Locations2 sites (Brest and 1 other locations)
StatusRecruiting
StartedOctober 22, 2024
Main results expectedJune 15, 2026
Study endsJune 15, 2026
Registry record updatedSeptember 16, 2025
Trial IDNCT06652204 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal participants are adult (18+) family caregivers or household members of a patient with COPD in stable condition who can read and complete French questionnaires and who provide non-opposition to participate.

Probably not a fit

Caregivers who cannot complete French questionnaires, who are under judicial protection, whose patient had a recent exacerbation, or who care for patients with cognitive impairment are excluded and therefore unlikely to benefit from participation.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational validation project adapts and tests the Portuguese QASCI questionnaire in French-speaking caregivers of patients with COPD. Caregivers who meet inclusion criteria will complete the French QASCI and related measures at participating centers in Brittany. The study will examine linguistic and cultural fit and use standard psychometric analyses (reliability, internal consistency, and construct validity) to determine whether the translated questionnaire performs acceptably. Recruitment and data collection occur at the University Hospital of Brest and the Centre Hospitalier de Morlaix.

Why it matters

Potential benefit: If successful, clinicians and researchers will have a validated French tool to measure caregiver burden and better target support services.

How similar studies have gone: The QASCI was originally validated in Portuguese (Hipolito et al.) and has been used in other language adaptations, so this is a linguistic and cultural validation of an established instrument rather than a wholly novel concept.

Who can join: the full rules

Show full inclusion / exclusion criteria
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.

Where it's running

  • Chu Brest
    Brest, France
    Recruiting
  • Centre hospitalier de Morlaix
    Morlaix, France
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.