Actively Recruiting

Phase Not Applicable
Age: 18Years - 50Years
FEMALE
Healthy Volunteers
NCT05614661

Postpartum Intervention for Mothers With Opioid Use Disorders

Led by Stony Brook University · Updated on 2024-12-16

50

Participants Needed

2

Research Sites

115 weeks

Total Duration

On this page

Sponsors

S

Stony Brook University

Lead Sponsor

U

University of Michigan

Collaborating Sponsor

AI-Summary

What this Trial Is About

Opioid use disorder (OUD) is a fast-growing and devastating epidemic in the US with many mothers suffering cravings, depression, impaired interpersonal interactions and maladaptive parenting behaviors that may lead to child maltreatment and costly utilization of foster care. This interdisciplinary multisite project will begin with the high risk R61 phase, in which the investigators will administer the parenting intervention "Mom Power" to mothers with OUD during the first 6 months postpartum and look for effects on drug use, mood and brain mechanisms; and, If validated, the investigators will continue in the R33 with more brain mechanism investigation and outcome studies a larger sample. The completion of this grant will clarify the effects of parenting intervention for mothers with OUD, and yield brain-based biomarkers that may be connected with inexpensive measures toward improved treatment of families suffering OUD, their children and society - which ultimately bears much of the cost for the common trans-generational problems of peripartum drug use.

CONDITIONS

Official Title

Postpartum Intervention for Mothers With Opioid Use Disorders

Who Can Participate

Age: 18Years - 50Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Mothers aged 18 to 50 years from SBU or UM diagnosed with opioid use disorder (OUD) or receiving medication assisted treatment such as buprenorphine or methadone
  • Have a child aged 5 years or younger
  • Able to read, hear, and understand English adequately to provide informed consent
Not Eligible

You will not qualify if you...

  • Require immediate clinical care for suicidal or homicidal risk or psychosis
  • For brain MRI, exclude if having ferromagnetic metal in the head
  • Severe claustrophobia preventing participation in MRI
  • Serious neurological conditions interfering with neuroimaging, such as brain tumor, multiple sclerosis, or significant head trauma
  • Exclusion from MRI does not necessarily exclude from the study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

University of Michigan

Ann Arbor, Michigan, United States, 48109

Actively Recruiting

2

Stony Brook University

Stony Brook, New York, United States, 11794

Actively Recruiting

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Research Team

E

Elle Eggers, BSc

CONTACT

D

Diana Saum, MA, MSW

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

2

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