Intervention for IPV Perinatal Women- RCT
Completed · Not applicable
Conditions studied: Intimate Partner Violence
In brief
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.
Key facts
- Study ID
- NCT02370394
- Run by
- Women and Infants Hospital of Rhode Island
- People needed
- 53
- Starts
- 2015-03-01
- Expected to finish
- 2016-09-01
- Last updated by the study team
- 2018-06-04
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- 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)
You may not qualify if…
- 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)
Where it is running
- Center for Women's Behavioral Health at Women and Infants' Hospital — Providence, Rhode Island, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.