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Comparison of patient reported disease activity scores combined with calprotectin home tests for remote monitoring of IBD patients: a cross-sectional cohort study

Recruiting
Conditions
inflammatory bowel diseases
10017969
Registration Number
NL-OMON54092
Lead Sponsor
niversiteit Maastricht
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
400
Inclusion Criteria

- Established diagnosis of CD or UC based on ECCO guidelines
- CD or UC patients scheduled for an ileocolonoscopy, or UC patients scheduled
for an sigmoidoscopy at the endoscopy ward of one of the participating centers
(regardless of indication)
- Aged 18 years or older
- Smartphone with internet access (for use of fecal calprotectin home test)

Exclusion Criteria

- Unclassified IBD
- Ileostomy, colostomy, ileoanal pouch anastomosis or ileorectal anastomosis
- Isolated upper gastro-intestinal CD, or isolated peri-anal disease
- Insufficient knowledge of Dutch language

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>The primary outcome is prediction of mucosal inflammation in daily clinical<br /><br>practice, using the below listed PROMs (with and without FC home test),<br /><br>relative to the gold standard ileocolonoscopy:<br /><br>- MIAH<br /><br>- Mobile health Index<br /><br>- Manitoba IBD index<br /><br>- IBD-control<br /><br>- p-HBI / p-SCCAI<br /><br><br /><br>In addition, redeveloped and optimized PROMs are a primary endpoint. </p><br>
Secondary Outcome Measures
NameTimeMethod
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