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Characterizing Adherence to Treatment and Satisfaction With Care in Patients With Cutaneous Lupus (ADlupus)

T

Toulouse University Hospital

Status

Enrolling

Conditions

Cutaneous Lupus

Treatments

Other: Questionnaires

Study type

Observational

Funder types

Other

Identifiers

NCT06506214
RC31/22/0298

Details and patient eligibility

About

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.

Full 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.

Enrollment

233 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 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

Exclusion criteria

  • 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

Trial design

233 participants in 1 patient group

Study group
Treatment:
Other: Questionnaires

Trial contacts and locations

4

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Central trial contact

Carle PAUL, MD

Data sourced from clinicaltrials.gov

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