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Clinical Trial Summary

The study team performed a randomized controlled trial to evaluate the efficacy of a care coordination intervention composed of proactive symptom monitoring and algorithm-based triggers to improve patient reported outcomes (PROs) and healthcare expenditures for high-risk patients with IBD. Enrolled patients with IBD were randomized to proactive symptom monitoring with the support of a care coordinator or usual care.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04796571
Study type Interventional
Source University of Michigan
Contact
Status Completed
Phase N/A
Start date January 1, 2019
Completion date March 1, 2020

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