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Clinical Trials/NCT00465556
NCT00465556CompletedPhase 2

Domestic Violence Enhanced Home Visitation Program - DOVE

Johns Hopkins University2 sites in 1 country239 target enrollmentStarted: February 1, 2006Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Phase 2
Status
Completed
Enrollment
239
Locations
2
Primary Endpoint
Reducing Intimate Partner Violence

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
Female
Accepts 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

Arms & Interventions

1

Experimental

Dove Intervention

Intervention: Public Health Nurse Home Visit (Behavioral)

2

Active Comparator

Intimate Partner Violence (IPV) Protocol

Intervention: Intimate Partner Violence (IPV) Protocol (Behavioral)

Outcomes

Primary Outcomes

Reducing Intimate Partner Violence

Time Frame: Baseline (entry into the study), birth of the infant, and 3, 6, 12 and 24 months after the infant's birth.

Reducing children's exposure to Intimate Partner Violence

Time Frame: Baseline (entry into the study), birth of the infant, and 3, 6, 12 and 24 months after the infant's birth.

Patterns of Intimate Partner Violence

Time Frame: Baseline (entry into the study), birth of the infant, and 3, 6, 12 and 24 months after the infant's birth.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Phyllis Sharps

Professor, Associate Dean

Johns Hopkins University

Study Sites (2)

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