Personally-Tailored Opioid-overdose and Medication for Opioid Use Disorder (MOUD) Education (TOME) for Pregnant and Postpartum Persons in MOUD

Completed · Not applicable

Conditions studied: Opioid Use Disorder, Pregnancy Related, Substance Use, Drug Abuse, Drug Abuse in Pregnancy, Drug Addiction

In brief

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.

Key facts

Study ID

NCT06262347

Run by

T. John Winhusen, PhD

People needed

131

Starts

2024-06-13

Expected to finish

2024-11-11

Last updated by the study team

2025-05-11

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Potential participants must be:
• 18 years of age or older;
• Pregnant or be within 12 months postpartum;
• Enrolled in MOUD (either buprenorphine or methadone) at the study site or affiliated clinic where enrollment can be confirmed;
• Able to understand the study, and having understood, provide written informed consent in English

You may not qualify if…

• Potential participants must not:
• have suicidal or homicidal ideation requiring immediate attention.

Where it is running

• Gateway Community Services — Jacksonville, Florida, United States
• Pregnancy Recovery Center at Magee-Womens Hospital of UPMC — Pittsburgh, Pennsylvania, United States
• Medical University of South Carolina — Charleston, South Carolina, United States
• Vanderbilt University Medical Center — Nashville, Tennessee, United States
• University of Utah SUPeRAD Clinic — Salt Lake City, Utah, United States
• Marshall Health MARC Program — Huntington, West Virginia, United States

Full record on ClinicalTrials.gov

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