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Domestic Violence Enhanced Home Visitation Program (DOVE)

Domestic Violence Enhanced Home Visitation Program - DOVE

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00465556
Enrollment
239
Registered
2007-04-25
Start date
2006-02-28
Completion date
2011-11-30
Last updated
2015-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Domestic Violence

Brief 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.

Interventions

BEHAVIORALPublic Health Nurse Home Visit

The 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) Protocol

The 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.

Sponsors

National Institute of Nursing Research (NINR)
CollaboratorNIH
Johns Hopkins University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Pregnant women 31 weeks or less gestation, over age 18, with a history of intimate partner violence within the past 2 years, and who are willing to participate in the home visit program

Exclusion criteria

Age 17 or less. History of partner violence beyond 2 years. Not participating in home visit program. Does not speak English

Design outcomes

Primary

MeasureTime frame
Reducing children's exposure to Intimate Partner ViolenceBaseline (entry into the study), birth of the infant, and 3, 6, 12 and 24 months after the infant's birth.
Patterns of Intimate Partner ViolenceBaseline (entry into the study), birth of the infant, and 3, 6, 12 and 24 months after the infant's birth.
Reducing Intimate Partner ViolenceBaseline (entry into the study), birth of the infant, and 3, 6, 12 and 24 months after the infant's birth.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026