Not medical advice. This website is not medical advice, a diagnosis, a match to a trial, or a recommendation to join a study. Listings are plain-English rewrites of public ClinicalTrials.gov records. Whether a site is still enrolling, and whether you qualify, can only be confirmed by the study team and your clinician. Source registry: ClinicalTrials.gov. Editorial rules: methodology.
RecruitingNot a traditional drug phaseinterventionalRules rewrite
Not a traditional drug phase: SFR application for Rhumatoid Arthisis
Rheumatoid arthritis (RA) and spondyloarthritis (SpA), including psoriatic arthritis (PsA), are chronic painful diseases that impair quality of life. Disease-modifying antirheumatic drugs (DMARDs) are used to control disease activity, reduce functional disability, and improve prognosis.
This study does not use the classic phase 1–4 drug ladder. It may be a device, a behavior program, a surgery timing study, or an early feasibility test.
Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.
What the registry says happens
If you join, the listed intervention(s) are SFR application. The registry lists allocation as randomized. Rheumatoid arthritis (RA) and spondyloarthritis (SpA), including psoriatic arthritis (PsA), are chronic painful diseases that impair quality of life.
They plan to enroll about 144 people at Paris. Taking part typically means using or being fitted with a device plus check-ins.
Official title (unrewritten)
Efficacy of a Self-Management Smartphone App in Promoting Safety Skills of Patients With Inflammatory Arthritis Treated by Anti-Rheumatic Drugs
Interventions: SFR application
Primary outcome (registry wording): safety skills regarding the use of tDMARDS
Who it is for (from inclusion criteria)
Ages 18 Years to 75 Years
Age between 18 and 75 years
Undergoing a treatment change to a tDMARD (biologic or JAK inhibitor) available in the SFR application
No therapeutic education on tDMARDs in the past two years
Ability to use a smartphone application
Ability to use a website
Ability to complete a questionnaire
Covered by social security or entitled to social protection
Who the registry excludes
Any condition that may affect comprehension or treatment adherence (chronic alcoholism, language barrier, severe psychiatric disorders, cognitive impairment)
Planned treatment with intravenous bDMARDs in the upcoming year
Patients who have already downloaded self-management applications for their rheumatic disease
Patients enrolled in a therapeutic education program: face-to-face education by a nurse or healthcare professional, or group education
Patients who have already received therapeutic education on targeted DMARDs in the past two years: face-to-face education by a nurse or healthcare professional, or group education
This study wants to obtain biologic materials from the blood, airways and/or urine of normal individuals and individuals with lung disease. The normal are used to establish a set of normal ranges for various parameters.
In a previous exploratory study, the investigators observed an effect on disease activity outcomes of anti-inflammatory diet. The investigators also observed change in microbiome and circulating metabolites.
The sponsor posted status “Recruiting” on ClinicalTrials.gov at last ingest. Sites can pause independently. Confirm with the official record and the listed contact.
What phase is NCT07460739?
Not a traditional drug phase. Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.
Can PlainTrials tell me if I qualify for NCT07460739?
No. The inclusion and exclusion lists on this page are readable extracts of the public eligibility block. Only the study team can screen you.