Domestic Violence Enhanced Home Visitation Program (DOVE)

NCT ID: NCT00465556

Last Updated: 2015-04-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE2

Total Enrollment

239 participants

Study Classification

INTERVENTIONAL

Study Start Date

2006-02-28

Study Completion Date

2011-11-30

Brief Summary

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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

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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

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Domestic Violence

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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1

Dove Intervention

Group Type EXPERIMENTAL

Public Health Nurse Home Visit

Intervention Type BEHAVIORAL

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.

2

Intimate Partner Violence (IPV) Protocol

Group Type ACTIVE_COMPARATOR

Intimate Partner Violence (IPV) Protocol

Intervention Type BEHAVIORAL

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.

Interventions

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Public 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.

Intervention Type BEHAVIORAL

Intimate 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.

Intervention Type BEHAVIORAL

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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National Institute of Nursing Research (NINR)

NIH

Sponsor Role collaborator

Johns Hopkins University

OTHER

Sponsor Role lead

Responsible Party

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Phyllis Sharps

Professor, Associate Dean

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Phyllis Sharps, PhD, RN

Role: PRINCIPAL_INVESTIGATOR

Johns Hopkins University

Locations

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Baltimore City Health Department

Baltimore, Maryland, United States

Site Status

Missouri Department of Health and Senior Services; Missouri Community Based Home Visiting Program and Lutheran and Family Children's Services in Columbia and Springfield

Columbia, Missouri, United States

Site Status

Countries

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United States

References

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Kalra N, Hooker L, Reisenhofer S, Di Tanna GL, Garcia-Moreno C. Training healthcare providers to respond to intimate partner violence against women. Cochrane Database Syst Rev. 2021 May 31;5(5):CD012423. doi: 10.1002/14651858.CD012423.pub2.

Reference Type DERIVED
PMID: 34057734 (View on PubMed)

Sharps PW, Bullock LF, Campbell JC, Alhusen JL, Ghazarian SR, Bhandari SS, Schminkey DL. Domestic Violence Enhanced Perinatal Home Visits: The DOVE Randomized Clinical Trial. J Womens Health (Larchmt). 2016 Nov;25(11):1129-1138. doi: 10.1089/jwh.2015.5547. Epub 2016 May 20.

Reference Type DERIVED
PMID: 27206047 (View on PubMed)

Sharps P, Alhusen JL, Bullock L, Bhandari S, Ghazarian S, Udo IE, Campbell J. Engaging and retaining abused women in perinatal home visitation programs. Pediatrics. 2013 Nov;132 Suppl 2(Suppl 2):S134-9. doi: 10.1542/peds.2013-1021L.

Reference Type DERIVED
PMID: 24187115 (View on PubMed)

Other Identifiers

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1R01NR009093-01A2

Identifier Type: NIH

Identifier Source: secondary_id

View Link

NR009093

Identifier Type: -

Identifier Source: org_study_id

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