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Clinical Trial Summary

This study aims to test the efficacy of a 4-session intervention (Group psychoeducational treatment) using a randomized study design. Participants will be randomized in to 'immediate treatment' or 'waitlist control'. Women in the wait-list condition will receive the 4-session IMPROVED treatment, just as women randomized to the experimental group, after the end of their wait-list period.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01704443
Study type Interventional
Source University of British Columbia
Contact
Status Completed
Phase N/A
Start date April 2008
Completion date April 2013

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