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Clinical Trial Summary

The primary objective of this study is to evaluate the ability of TOME to increase Medication for Opioid Use Disorder (MOUD) and opioid-overdose knowledge in pregnant and postpartum persons.


Clinical Trial Description

This is an intent-to-treat, two-arm, open-label, randomized controlled trial. Eligible participants will be randomized in a 1:1 ratio to TOME or Control, balancing on site. Participants will receive the assigned intervention following randomization and will complete a three week follow-up assessment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06262347
Study type Interventional
Source University of Cincinnati
Contact Frankie Kropp, MS
Phone 513-585-8290
Email kroppfb@ucmail.uc.edu
Status Recruiting
Phase N/A
Start date June 13, 2024
Completion date June 20, 2025

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