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CompletedNCT00465556

Domestic Violence Enhanced Home Visitation Program (DOVE)

Domestic Violence Enhanced Home Visitation Program - DOVE

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
239 (actual)
Sponsor
Johns Hopkins University · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Accepted

Summary

DOVE Home Visit Program is a brochure based intervention delivery by public health nurses which aims to prevent and reduce intimate partner violence against pregnant and postpartum women and their infants. The purpose of the study is to test the effect of home visits on reducing domestic violence and improving the lives of pregnant women and their children.

Detailed description

Outcomes will provide intervention efficacy data about a public health nurse home visit intervention aimed at reducing and preventing intimate partner violence and children's exposure to IVP as well as prospective information about patterns of intimate partner violence.

Conditions

Interventions

TypeNameDescription
BEHAVIORALPublic Health Nurse Home VisitThe perinatal public health nurse home visit intervention also includes a trifold brochure, printed on 8X10 inch paper, with 6 panels, that can be read with the woman in an interactive manner so that the woman is encouraged to describe her experiences and choose her options as they proceed. Participants will receive three prenatal and three postpartum sessions. The first prenatal sessions will be given during the first (enrollment), second, and third trimesters, with at least three weeks between sessions. Women entering the study after the first trimester will receive the initial session at enrollment, with two subsequent sessions spread out over the remainder of the scheduled prenatal home visitation program sessions.
BEHAVIORALIntimate Partner Violence (IPV) ProtocolThe current protocol in use by the participating health departments when a women screens positive for intimate partner violence (IPV), current or history within the last year.

Timeline

Start date
2006-02-01
Primary completion
2010-11-01
Completion
2011-11-01
First posted
2007-04-25
Last updated
2015-04-03

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00465556. Inclusion in this directory is not an endorsement.