Questionnaire: Patients are asked to complete several questionnaires
Study summary
The purpose of this study is to develop a French language version of the Compliance-Questionnaire-Rheumatology for use in French and Francophone rheumatology services
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* The patient must have given their free and informed consent and signed the consent form
* The patient must be a member or beneficiary of a health insurance plan
* The patient is at least 18 years old
* The patient has rheumatoid polyarthritis as defined by the ACR-EULAR 2010 criteria, treated orally or subcutaneously with MTX for at least 3 months with a stable (unchanged) dosage for at least 1 month, and a stable (unchanged) route of administration for at least 1 month. And no planned change in Methotrexate intake at least until the second study visit. Other treatments at the same time are authorized
Exclusion Criteria:
* The subject is participating in an interventional study, or is in a period of exclusion determined by a previous study
* The subject refuses to sign the consent
* It is impossible to give the subject informed information
* The patient is under safeguard of justice or state guardianship
* The subject has a contraindication to taking methotrexate (including a patient with a desire to become pregnant).
Primary outcome measure(s)
Test-retest agreement of French translation of the Compliance Questionnaire Rheumatology questionnaire — 40 minutes Intraclass correlation and Kappa coefficient of 2 evaluations taken 40 minutes apart
Structural validity of French translation of the Compliance Questionnaire Rheumatology questionnaire — Baseline Principal component analysis
Trial sites (4)
Facility
City
Region
Status
CHU Bordeaux
Bordeaux
France
Not Yet Recruiting
CHRU Montpellier
Montpellier
France
Not Yet Recruiting
CHU Nimes
Nîmes
France
Recruiting
CHU Toulouse
Toulouse
France
Not Yet Recruiting
More Centre Hospitalier Universitaire de Nīmes trials in France
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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