Patient preference for colorectal cancer surveillance strategy in inflammatory bowel disease: a discrete choice experiment
Completed
- Conditions
- Inflammatory bowel disease, IBD, Crohn's disease, ulcerative colitis
- Registration Number
- NL-OMON29540
- Lead Sponsor
- MC Utrecht
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 400
Inclusion Criteria
Diagnosis of IBD (Crohn’s disease, ulcerative colitis, IBD-unclassified)
- Age = 18 years
- Signed informed consent
- Fulfilling criteria to undergo surveillance colonoscopy according to the Dutch IBD guidelines
Exclusion Criteria
Potential subjects who meet any of the following criteria will be excluded from participation from this study:
- No signed informed consent
- Insufficient knowledge of the Dutch language or illiteracy to independently complete the questionnaire
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.To determine patients’ preferences with respect to colonoscopic surveillance intervals.
- Secondary Outcome Measures
Name Time Method 1.To assess the relative importance of disease-related and psychosocial factors, driving the patients’ preferences on CRC surveillance intensity.<br>2.To compare the preferred surveillance intervals between IBD patients treated in a non-academic hospital or in an academic hospital. <br>3.To identify differences in preference structures among subgroups in the IBD cohort (e.g. disease duration, positive versus negative family history of CRC)