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Clinical Trial Summary

The aim of this study is to test the feasibility and effectiveness of a 16-week online behavioral weight loss program compared to usual care to promote weight loss in the postpartum period among women with cardiovascular risk factors. The investigators will also be testing different behavioral strategies to recruit postpartum women to the study, including 2 email recruitment strategies and 2 mailer recruitment strategies, informed by behavioral design.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04914819
Study type Interventional
Source University of Pennsylvania
Contact
Status Completed
Phase N/A
Start date June 18, 2021
Completion date December 31, 2021

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