Status:
RECRUITING
Clinical Trial to Reduce Perinatal Intimate Partner Violence
Lead Sponsor:
University of Pittsburgh
Collaborating Sponsors:
National Institute of Nursing Research (NINR)
Conditions:
Domestic Violence
Perinatal Problems
Eligibility:
FEMALE
18+ years
Phase:
NA
Brief Summary
This is a two-armed, fully powered hybrid type 1 trial to test the effectiveness of a doula intervention compared with an active control in reducing intimate partner violence (IPV) among perinatal IPV...
Detailed Description
The study team will complete a 2-arm randomized clinical trial to test the effectiveness of IPV-trained doulas compared with an active control in reducing IPV among perinatal IPV survivors. Participan...
Eligibility Criteria
Inclusion
- Perinatal IPV survivors are eligible if they:
- 1\) feel comfortable completing the study in Spanish or English
- 2\) are age 18 or older
- 3\) are no more than 22 weeks gestation
- 4\) identify as an IPV survivor by answering affirmatively to a definition of experiencing IPV
- 5\) live within a 50 mile radius of Pittsburgh, Pennsylvania
- 6\) able to provide safe and complete contact information or take a study cell phone
Exclusion
- Unable to consent
- Do not meet inclusion criteria
- Cannot provide safe contact information or take a study cell phone
- Incarcerated
Key Trial Info
Start Date :
November 1 2025
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
October 1 2029
Estimated Enrollment :
326 Patients enrolled
Trial Details
Trial ID
NCT07165860
Start Date
November 1 2025
End Date
October 1 2029
Last Update
December 4 2025
Active Locations (3)
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1
Magee Women's Hospital
Pittsburgh, Pennsylvania, United States, 15213
2
The Midwife Center
Pittsburgh, Pennsylvania, United States, 15222
3
Family Medicine Department
Pittsburgh, Pennsylvania, United States, 15260