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Study identifier: NCT04939012 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Implementation of a Patient-centered, Reproductive Planning Decision Support Tool (MyPath) Among Women With Substance Use Disorder in the Immediate Postpartum Period

Condition: Substance Use Disorders · Pregnancy Related · Contraception  ·  Sponsor: University of Pittsburgh

PhaseNA
Planned participants400
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

This is a study to determine the effect of a novel patient-centered, reproductive planning decision support tool developed by the research team called MyPath on postpartum contraceptive decision-making among women with SUDs.

This description comes directly from the study's public registry record.

Talk to the study team

Elizabeth Krans, MD  ·  (412) 641-3532  ·  kransee@upmc.edu

Samantha Mayo, BA  ·  (412) 641-2248  ·  mayos@upmc.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Magee Womens Hospital of UPMCPittsburgh, Pennsylvania, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT04939012