Occupational Insertion and Educational Level of Adult Patients With Pediatric Early Inflammatory Bowel Disease (IBD)

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

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)

Eligibility
Participation Requirements
Sex: All
Minimum Age: 25
Healthy Volunteers: f
View:

• Male or female, aged 25 and over at the time of the study

• Subject listed in the EPIMAD registry suffering from certain or probable Crohn's disease, or certain or probable ulcerative colitis, or certain or probable ulcerated proctitis, unclassified colitis, diagnosed between 01/01 / 1988 and 12/31/2011, with an age at diagnosis of less than 17 years (definition of the pediatric cohort of the EPIMAD Registry)

• Patient residing in the area of the EPIMAD registry: Nord, Pas-de-Calais, Somme or Seine-Maritime

• Patient not opposed to the research

• Patient not having objected to the use of their data for ancillary studies when registering in the EPIMAD register

Locations
Other Locations
France
Hop Jeanne de Flandre Chu Lille
RECRUITING
Lille
Contact Information
Primary
Dominique Turck, MD,PhD
Dominique.Turck@CHRU-Lille.fr
320446885
Time Frame
Start Date: 2019-11-28
Estimated Completion Date: 2026-01
Participants
Target number of participants: 460
Sponsors
Collaborators: Ministry of Health, France
Leads: University Hospital, Lille

This content was sourced from clinicaltrials.gov