N/A
N=53
Intervention for IPV Perinatal Women- RCT
Intimate Partner Violence
Bottom Line
View on ClinicalTrials.gov: NCT02370394 ↗Enrolled (actual)
53
Serious AEs
28.3%
Results posted
Jan 2018
Primary outcome: Primary: Composite Abuse Scale (CAS)-CAS Victimization Total Score — 26.36; 16.56; 12.38; 16.52 units on a scale — p=0.4016
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- ROSE Program (Behavioral)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- Female
- Sponsor
- Women and Infants Hospital of Rhode Island
- Primary completion
- Sep 2016
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Composite Abuse Scale (CAS)-CAS Victimization Total Score |
26.36; 16.56; 12.38; 16.52 | 0.4016 |
| PRIMARY Safety Behavior Checklist (SBC) |
.28; .36; .28; .32 | 0.6011 |
| PRIMARY Effectiveness in Obtaining Resources Scale (EOR) |
2.46; 3.48; 3.31; 3.43 | 0.8646 |
| SECONDARY Motivation Scale |
6.18; 7.52; 6.81; 7.22 | 0.9085 |
| SECONDARY The Readiness to Change Contemplation Ladder |
8.25; 8.08; 8.00; 7.26 | 0.4085 |
Summary
The study developed and assessed an innovative, high-reach, easily implementable, low-cost computer-delivered intervention (Reach out for a Safe Environment; ROSE Program) that addressed known barriers in early identification and intervention with perinatal women with IPV seeking treatment for mental illness.
Eligibility Criteria
Inclusion Criteria
- Pregnant or postpartum women (up to 6 months after delivery)
- Age 18 or older
- Seeking mental health treatment at The Center for Women's Behavioral Health (WBH) at Women and Infants Hospital (WIH)
- Endorsed any IPV during the past 12 months as measured by the Woman Abuse Screening Tool (WAST)
Exclusion Criteria
- Inability to provide informed consent (e.g., due to psychosis, intoxication, or other clear cognitive impairment)
- Inability to understand English (understand the consent form when read aloud and assessments that are narrated by computer)
Data sourced from ClinicalTrials.gov (NCT02370394). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.