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NCT07634354
Sarcopenia and Juvenile Idiopathic Arthritis
Conditions: Juvenile Idiopathic Arthritis
Sex: All
Ages: 15 Years – 40 Years
Healthy volunteers: No
Phase: NA
Enrollment: 200
Sponsor: CHU de Reims
Location: Marie Muller Reims
Summary
Juvenile idiopathic arthritis (JIA) is a rare chronic inflammatory rheumatic disease that begins during childhood and may persist into adulthood in many patients. In addition to joint pain, swelling, and long-term articular damage, chronic inflammatory diseases may also be associated with early sarcopenia, defined as a loss of muscle strength and muscle mass. While this association has been described in adult inflammatory rheumatic diseases, it has not been well studied in patients with JIA.
The aim of this study is to screen for sarcopenia in adolescents and adults with JIA in France. Sarcopenia will be assessed using validated questionnaires, hand grip strength measured with a Jamar dynamometer, and body composition measured by dual-energy X-ray absorptiometry (DEXA). Completion of validated questionnaires will assess nutritional status, fatigue, physical activity, and functional impact. Socio-demographic and clinical data will also be collected from medical records.
This multicenter cross-sectional study will be conducted between June 2026 and October 2027 in 11 French hospitals. Eligible participants are patients aged 15 to 40 years with JIA diagnosed according to ILAR criteria and followed in a French hospital.
This study will provide the first estimate of sarcopenia prevalence among patients with JIA in France. It will also help identify factors associated with sarcopenia and its impact on daily functioning and quality of life. In the longer term, the findings may help clinicians better identify patients at risk and support earlier management focused on disease control, physical activity, and nutritional care.
Eligibility Criteria
inclusion criteria :
* Patients followed in French hospitals participating in the study for juvenile idiopathic arthritis, all forms combined, diagnosed according to the ILAR criteria defined in Edmonton in 2001
* Patients aged 15 to 40 years
* Affiliated to social security
* Agreeing to participate in the study and having given their written consent (signed consent form).
In the case of a minor patient, the consent of the patient and their legal guardians is required.
exclusion criteria :
* Patient under legal guardianship
* Patient not covered by social security
* Pregnant woman
* Inability to perform a functional test required by the study (grip test or whole-body DEXA scan)
* Inability to understand the questionnaires
Source: ClinicalTrials.gov (NCT07634354). StuddyBuddy aggregates publicly available trial information.