Interdisciplinary Care of Pediatric Patients with Chronic Inflammatory Bowel Disease

Not Applicable

Conditions: Chronic Inflammatory Bowel Disease

Registration Number: DRKS00017216

Lead Sponsor: niversität Leipzig

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Pending

Sex: All

Target Recruitment: 58

Inclusion Criteria

Written consent of the patient (from 14 years) and parents (or the custodian) to participate in the study and the related survey and storage of data
- Age of patients is at least 6 years
- Chronic inflammatory bowel disease of any form (Morbus Crohn, Colitis Ulcerosa, IBDU- Inflammatory Bowel Disease Unclassified)
- Knowledge of the German language required for study participation

Exclusion Criteria

- Rejection of participation by the patient or the parents (or the custodian)
- Rejection of participation by the treating physician of the study centre
- No fulfillment of the other inclusion criteria

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
- Number of drug-related problems in the handling skills of long-term medications and the knowledge about this long-term medication of the respective patient patient after one year <br>- measured by means of a observation form and a questionnaire

Secondary Outcome Measures

Name	Time	Method
- Change in PUCAI/PCDAI (Pediatric Ulcerative Colitis Activity Index/Pediatric Crohn's Disease Activity Index) depending on disease classification <br>- Change in calprotectin <br>- Increased adherence <br>- Improvement of the quality of life <br>- Number of days absent from school <br>- Attitude towards drug therapy (acceptance) <br>- Patient satisfaction and problems with medication<br>- (Re)hospitalization rate <br>- Number of discrepancies between physician's/parents' assessment on adherence to therapy and the assessment by the patient<br>- Number of prescriptions for drugs to treat chronic inflammatory bowel disease filled at a pharmacy and the time at which the prescription was filled <br>- these routinely documented data are collected after one year from the patient's medical record using a data collection sheet; data on quality of life are assessed by using the KINDL-questionnaire