Domestic Violence Enhanced Home Visitation Program (DOVE)
2 other identifiers
interventional
239
1 country
2
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for phase_2
Started Feb 2006
Longer than P75 for phase_2
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2006
CompletedFirst Submitted
Initial submission to the registry
April 23, 2007
CompletedFirst Posted
Study publicly available on registry
April 25, 2007
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2010
CompletedStudy Completion
Last participant's last visit for all outcomes
November 1, 2011
CompletedApril 3, 2015
March 1, 2015
4.8 years
April 23, 2007
March 31, 2015
Conditions
Outcome Measures
Primary Outcomes (3)
Reducing children's exposure to Intimate Partner Violence
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
Baseline (entry into the study), birth of the infant, and 3, 6, 12 and 24 months after the infant's birth.
Reducing Intimate Partner Violence
Baseline (entry into the study), birth of the infant, and 3, 6, 12 and 24 months after the infant's birth.
Study Arms (2)
1
EXPERIMENTALDove Intervention
2
ACTIVE COMPARATORIntimate Partner Violence (IPV) Protocol
Interventions
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.
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.
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- Age 17 or less. History of partner violence beyond 2 years. Not participating in home visit program. Does not speak English
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Baltimore City Health Department
Baltimore, Maryland, 21205, United States
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, 65211, United States
Related Publications (3)
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.
PMID: 34057734DERIVEDSharps 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.
PMID: 27206047DERIVEDSharps 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.
PMID: 24187115DERIVED
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Phyllis Sharps, PhD, RN
Johns Hopkins University
Study Design
- Study Type
- interventional
- Phase
- phase 2
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor, Associate Dean
Study Record Dates
First Submitted
April 23, 2007
First Posted
April 25, 2007
Study Start
February 1, 2006
Primary Completion
November 1, 2010
Study Completion
November 1, 2011
Last Updated
April 3, 2015
Record last verified: 2015-03