Actively Recruiting
Validation of the French Version of the CQR (Compliance Questionnaire Rheumatology)
Led by Centre Hospitalier Universitaire de Nīmes · Updated on 2025-12-03
150
Participants Needed
4
Research Sites
349 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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
CONDITIONS
Official Title
Validation of the French Version of the CQR (Compliance Questionnaire Rheumatology)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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
- No planned change in Methotrexate intake at least until the second study visit
- Other treatments at the same time are authorized
You will not qualify if you...
- 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)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 4 locations
1
CHU Bordeaux
Bordeaux, France, 33000
Not Yet Recruiting
2
CHRU Montpellier
Montpellier, France, 34295
Not Yet Recruiting
3
CHU Nimes
Nîmes, France, 30029
Actively Recruiting
4
CHU Toulouse
Toulouse, France, 31300
Not Yet Recruiting
Research Team
C
Cécile Gaujoux Viala, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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