Actively Recruiting
Occupational Insertion and Educational Level of Adult Patients With Pediatric Early Inflammatory Bowel Disease (IBD)
Led by University Hospital, Lille · Updated on 2025-12-23
460
Participants Needed
1
Research Sites
318 weeks
Total Duration
On this page
Sponsors
U
University Hospital, Lille
Lead Sponsor
M
Ministry of Health, France
Collaborating Sponsor
AI-Summary
What this Trial Is About
The main objective of this project is to assess the occupational insertion of these adult patients with pediatric-onset IBD and to compare it with the general population. The secondary objectives are: 1. to assess the level of education and compare it to that of the general population 2. to assess occupational insertion and the educational level according to: * The disease (Crohn's disease, ulcerative colitis or unclassified colitis) * sex * Age at diagnosis (\<or ≥ 10 years) * The occurence of surgery, the location of the disease, the treatments undertaken * Quality of life 3. Evaluate the patient's feelings about the impact of his illness on occupational insertion and the educational level 4. To describe the quality of life of patients in relation to disease activity and health states (QALY calculation) 5. To assess the responsivness to change of the functional handicap score IBD-DI (n = 200 patients)
CONDITIONS
Official Title
Occupational Insertion and Educational Level of Adult Patients With Pediatric Early Inflammatory Bowel Disease (IBD)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Male or female, aged 25 and over at the time of the study
- Registered in the EPIMAD registry with certain or probable Crohn's disease, ulcerative colitis, ulcerated proctitis, or unclassified colitis diagnosed before age 17 between 01/01/1988 and 12/31/2011
- Residing in the Nord, Pas-de-Calais, Somme, or Seine-Maritime areas
- Not opposed to participating in research
- Has not objected to the use of their data for ancillary studies when registered in the EPIMAD registry
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Hop Jeanne de Flandre Chu Lille
Lille, France, 59037
Actively Recruiting
Research Team
D
Dominique Turck, MD,PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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