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Impact of Collaborative Care for Pregnant Women With Opioid Use Disorder in Low-Resource Obstetric Settings (NEST)

University of Pittsburgh logo

University of Pittsburgh

Status

Begins enrollment in a year or more

Conditions

Opioid Use Disorder
Postpartum Period
Pregnancy

Treatments

Behavioral: Adapted Collaborative Care Model (CCM)
Behavioral: Usual Care Group

Study type

Observational

Funder types

Other
NIH

Identifiers

NCT06956352
R61DA061377 (U.S. NIH Grant/Contract)
STUDY24030140

Details and patient eligibility

About

The investigators seek to adapt a collaborative care model (CCM) for community-based, low-resource obstetric settings and to test the effects of this adapted CCM on health outcomes among Pregnant, postpartum, and parenting person (PPPP) with Opioid use disorder (OUD) and their families. To achieve this goal, investigators will conduct a nonrandomized, Type 1 hybrid implementation-effectiveness study across 3 community-based, low-resource obstetric sites in Northwest PA, a region with rates of maternal opioid-related diagnoses 4 times higher than national averages.

Full description

Our central hypothesis is that person-centered, recovery supports, provided in the CCM will increase medication for OUD (MOUD) initiation and continuation, decrease overdose and reduce child removal rates among PPPP with OUD.

Specifically, investigators will:

  1. Conduct an intervention adaptation project to adapt the Pregnancy and Women's Recovery Center (PWRC) CCM for rural and low-resource obstetric settings; and
  2. Create a common data model to harmonize variables across data sources and data collection processes across study sites.

Investigators will also:

  1. Evaluate the effects of the adapted PWRC CCM on outcomes among PPPP with OUD;
  2. Determine if improvements in person-centered, recovery supports mediate the relationship between PWRC Community and outcomes using causal mediation methods; and
  3. Identify PWRC Community adaptations that are associated with increased MOUD access, improved outcomes and that facilitate sustainability and scalability.

Research findings will:

  1. provide high-quality evidence on how CCMs affect service delivery and health outcomes for PPPP with OUD,
  2. inform stakeholders about ways to adapt CCMs for low-resource and rural healthcare settings, and
  3. inform policymakers about the adaptations necessary to replicate these models widely.

Enrollment

1,350 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

(Stakeholder Participant)

  1. 18 years or older
  2. Providing care at participating obstetric site
  3. English speaking

(Patient Participant)

  1. 18 years or older
  2. Receiving care at participating obstetric site
  3. English speaking

Exclusion criteria

  1. Unwillingness to have participation audio recorded.

Trial design

1,350 participants in 1 patient group

UPMC
Description:
Those receiving care at UPMC facilities
Treatment:
Behavioral: Usual Care Group
Behavioral: Adapted Collaborative Care Model (CCM)

Trial contacts and locations

1

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Central trial contact

Samantha M Mayo, BA

Data sourced from clinicaltrials.gov

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