Clinical Trial to Reduce Perinatal Intimate Partner Violence
Trial Parameters
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 survivors
Eligibility Criteria
Inclusion Criteria: 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 Criteria: * Unable to consent * Do not meet inclusion criteria * Cannot provide safe contact information or take a study cell phone * Incarcerated