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Clinical Trial to Reduce Perinatal Intimate Partner Violence

NCT07165860 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 250

Last updated 2026-04-16

No results posted yet for this study

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 survivors

Conditions

  • Domestic Violence
  • Perinatal Problems

Interventions

BEHAVIORAL

Doulas

The intervention will be pairing intimate partner violence survivors with a trained doula

BEHAVIORAL

Thrive

The active control arm will include pairing intimate partner violence survivors with IPV advocates

Sponsors & Collaborators

  • National Institute of Nursing Research (NINR)

    collaborator NIH

  • University of Pittsburgh

    lead OTHER

Principal Investigators

  • Maya I Ragavan · University of Pittsburgh

  • Dara Mendez · University of Pittsburgh

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-11-01
Primary Completion
2028-11-01
Completion
2029-05-01

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07165860 on ClinicalTrials.gov