Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
NCT04939012

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

Led by University of Pittsburgh · Updated on 2026-02-17

400

Participants Needed

1

Research Sites

228 weeks

Total Duration

On this page

Sponsors

U

University of Pittsburgh

Lead Sponsor

N

National Institute on Drug Abuse (NIDA)

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Be 18 years of age or older
  • Be pregnant with an estimated gestational age of 22 to 37 weeks at enrollment (Prenatal Cohort)
  • Plan to deliver at the research site (Prenatal Cohort)
  • Meet DSM-5 criteria for a substance use disorder or have a substance use disorder diagnosis in medical records
  • Be 18 years of age or older (Postpartum Cohort)
  • Be 0 to 9 days postpartum at enrollment (Postpartum Cohort)
  • Have delivered at the research site (Postpartum Cohort)
Not Eligible

You will not qualify if you...

  • Have experienced fetal or neonatal death with the current pregnancy
  • Be currently in jail or prison as required by law (probation or residential facilities allowed)
  • Have any social or medical condition that the Investigator believes would make participation unsafe or difficult
  • Have had a documented tubal ligation or hysterectomy at time of delivery hospitalization (Postpartum Cohort only)

AI-Screening

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Trial Site Locations

Total: 1 location

1

Magee Womens Hospital of UPMC

Pittsburgh, Pennsylvania, United States, 15213

Actively Recruiting

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Research Team

E

Elizabeth Krans, MD

CONTACT

S

Samantha Mayo, BA

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

2

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