Postpartum Intervention for Mothers With Opioid Use Disorders (R33)
Recruiting now · Not applicable
Conditions studied: Opioid Use Disorder, Parent-Child Relations
In brief
Having met the milestones of the R61, this R33 is a 2-site, 2-group, pre/post RCT of mothers with OUD (n=\~80/group). We will test whether the beneficial pre-post changes in OUD mothers randomized to vMP exceed those of mothers assigned to Enhanced Usual Care (EUC) and via changes in Maternal Brain Neurocircuits.
Key facts
- Study ID
- NCT07632053
- Run by
- Stony Brook University
- People needed
- 80
- Starts
- 2025-07-01
- Expected to finish
- 2028-07-01
- Last updated by the study team
- 2026-06-09
Who can join
Age: 18 and older, up to 50. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- mothers with diagnosis of Opioid Use Disorder (OUD); and/or receiving medication assisted treatment (such as buprenorphine or methadone)
- with a child aged 5 or less
- able to read, hear and understand English adequately enough to provide informed consent
You may not qualify if…
- require immediate clinical care for suicidal/homicidal risk or psychosis;
- For magnetic resonance imaging (MRI) of the brain, potential participants will be excluded if they: (1) have ferromagnetic metal in their heads (2) have severe claustrophobia that prevents participation in the neuroimaging (3) have serious neurological condition that could interfere with neuroimaging, including a brain tumor, multiple sclerosis or significant head trauma
Where it is running
- University of Michigan — Ann Arbor, Michigan, United States (enrolling)
- Stony Brook University — Stony Brook, New York, United States (enrolling)
Full record on ClinicalTrials.gov
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