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Clinical Trial Summary

The purpose of this protocol is:

1. To quantify the prevalence of adherence to topical mesalamine in patients with UC

2. To describe the determinants of medication adherence in patients with UC prescribed topical mesalamine


Clinical Trial Description

Patient adherence with topical mesalamine is low. Behavioral and psycho-social barriers to topical mesalamine adherence exist in patients with UC. These factors can be identified using qualitative testing in order to develop and design appropriate behavioral interventions to reduce non-adherence.

The investigators will undertake an observational study of medication persistence in 100 patients in the BIDMC clinic, "Persistence Cohort". Persistence will be measured using 12-month pharmacy refill data. The investigators will also employ a qualitative research design with discrete choice modeling in two phases: Phase I - Initial Interviews with 10 patients and Phase II - Focus Groups (2) with 5 patients each. ;


Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT01678300
Study type Observational
Source Beth Israel Deaconess Medical Center
Contact
Status Completed
Phase N/A
Start date August 2012
Completion date November 2015

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