Characterizing Adherence to Treatment and Satisfaction With Care in Patients With Cutaneous Lupus
- Conditions
- Cutaneous Lupus
- Interventions
- Other: Questionnaires
- Registration Number
- NCT06506214
- Lead Sponsor
- University Hospital, Toulouse
- Brief Summary
This multicenter study aims to evaluate treatment adherence and satisfaction of patients with cutaneous lupus, influenced by perception of the disease, fear of side effects, cost of medications and the doctor-patient relationship. Adherence will be measured by a VAS of 80% or higher on the Medical Adherence Self-Report Inventory scale.
- Detailed Description
This multicenter, cross-sectional study aims to characterize adherence to treatment and satisfaction of patients with cutaneous lupus. Non-adherence to treatment is a major problem, influenced by perception of the disease, fear of adverse effects, cost of medications and the doctor-patient relationship. Adherence will be measured by a VAS of 80% or more on the visual analog scale of the Medical Adherence Self-Report Inventory questionnaire.
The study is descriptive, multicenter and cross-sectional. Participants will be adult patients suffering from cutaneous lupus, diagnosed by a dermatologist and under treatment, able to complete questionnaires. Patients with systemic lupus, cognitive or psychiatric disorders will be excluded from the study.
The inclusion period is two years, with 30 minutes of follow-up per participant. The study will provide a better understanding of the feelings of patients with cutaneous lupus and the factors limiting their adherence to treatment.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- Female
- Target Recruitment
- 233
- Patients with cutaneous lupus (pure cutaneous or subacute) diagnosed by a dermatologist and under local and/or systemic treatment for cutaneous lupus
- No opposition to participation
- Patient able to complete the questionnaires
- Adult patient
- Systemic lupus with multiple visceral involvement
- Cognitive or psychiatric disorders preventing the smooth running of the study
- Pregnant woman
- Patient under guardianship/curatorship or safeguard of justice
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Study group Questionnaires -
- Primary Outcome Measures
Name Time Method Evaluation of adherence to treatment of patients with cutaneous lupus. Inclusion day Adherence is defined by a VAS greater than or equal to 80% on the Visual Analog Scale of the MASRI (Medical Adherence Self-Report Inventory) questionnaire.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (4)
University Hospital Montpellier
🇫🇷Montpellier, France
Hôpital Tenon
🇫🇷Paris, France
APHP Hôpital Saint-Louis
🇫🇷Paris, France
University Hospital Toulouse
🇫🇷Toulouse, France