Intervention for IPV Perinatal Women- RCT

NACompletedINTERVENTIONAL
Enrollment

53

Participants

Timeline

Start Date

March 31, 2015

Primary Completion Date

September 30, 2016

Study Completion Date

September 30, 2016

Conditions
Intimate Partner Violence
Interventions
BEHAVIORAL

ROSE Program

The ROSE Program was specifically tailored, innovative and relevant to diverse, racial and ethnic perinatal women in a number of ways including the images and content used in the intervention and coordinating study appointments with treatment visits. It was tailored to the current IPV risk assessment, pregnancy or postpartum status of each participant, was designed to reach participants across levels of motivation for change. The content of ROSE was theory-driven, consistent with the Motivational Interviewing model of behavior, and consistent with the literature on effective interventions that address IPV.

Trial Locations (1)

02905

Center for Women's Behavioral Health at Women and Infants' Hospital, Providence

All Listed Sponsors
collaborator

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

NIH

lead

Women and Infants Hospital of Rhode Island

OTHER

NCT02370394 - Intervention for IPV Perinatal Women- RCT | Biotech Hunter | Biotech Hunter