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Study identifier: NCT07469787 Synced from ClinicalTrials.gov · July 29, 2026
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Compassionate Care and Organization of Healthcare Services for a Successful Transition in Rheumatology

Condition: Chronic Inflammatory Rheumatic Diseases of Childhood · Juvenile-Onset Chronic Inflammatory Rheumatic Diseases · Transition of Care in Chronic Inflammatory Rheumatic Diseases  ·  Sponsor: Assistance Publique - Hôpitaux de Paris

PhaseN/A
Planned participants50
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The transition from pediatric to adult care is a critical period for young people with chronic inflammatory rheumatic diseases (CIRD) and is associated with risks of poor self-management, loss to follow-up, and disease worsening. Although structured transition programs have been recommended, real-world data on their effectiveness in rheumatology remain limited. Since 2018, a structured transition program has been implemented at Bicêtre University Hospital (AP-HP, France), combining early transition preparation, a therapeutic patient education (TPE) workshop, and a joint pediatric-adult transition consultation. Some patients benefit from both components, while others receive a transition consultation only. The BOOST-R study is a monocentric, non-interventional observational study designed to evaluate the impact of different transition modalities on self-management after transfer to adult care. The primary objective is to compare transition readiness, assessed using the validated French version of the Transition Readiness Assessment Questionnaire (TRAQ-FR), between patients who received a TPE workshop plus a transition consultation and those who received a transition consultation only. Secondary objectives include evaluating continuity of care after transition, identifying factors associated with successful transition, assessing the contribution of the RESRIP support network, and describing patients who did not benefit from structured transition support.

This description comes directly from the study's public registry record.

Talk to the study team

Perrine DUSSER, MD PhD  ·  145213146  ·  perrine.dusser@aphp.fr

Always discuss trial participation with your own doctor first.

Locations (1)

CHU BicêtreLe Kremlin-Bicêtre, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT07469787