Domestic Violence Enhanced Home Visitation Program (DOVE)

This study has been completed.
Sponsor:
Collaborator:
Information provided by (Responsible Party):
Phyllis Sharps, Johns Hopkins University
ClinicalTrials.gov Identifier:
NCT00465556
First received: April 23, 2007
Last updated: March 31, 2015
Last verified: March 2015
  Purpose

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.


Condition Intervention Phase
Domestic Violence
Behavioral: Public Health Nurse Home Visit
Behavioral: Intimate Partner Violence (IPV) Protocol
Phase 2

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Prevention
Official Title: Domestic Violence Enhanced Home Visitation Program - DOVE

Resource links provided by NLM:


Further study details as provided by Johns Hopkins University:

Primary Outcome Measures:
  • 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. ] [ Designated as safety issue: Yes ]
  • 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. ] [ Designated as safety issue: Yes ]
  • 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. ] [ Designated as safety issue: Yes ]

Enrollment: 239
Study Start Date: February 2006
Study Completion Date: November 2011
Primary Completion Date: November 2010 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: 1
Dove Intervention
Behavioral: 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.
Active Comparator: 2
Intimate Partner Violence (IPV) Protocol
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.

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.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Criteria

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

  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00465556

Locations
United States, Maryland
Baltimore City Health Department
Baltimore, Maryland, United States, 21205
United States, Missouri
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, 65211
Sponsors and Collaborators
Johns Hopkins University
Investigators
Principal Investigator: Phyllis Sharps, PhD, RN Johns Hopkins University
  More Information

No publications provided by Johns Hopkins University

Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Phyllis Sharps, Professor, Associate Dean, Johns Hopkins University
ClinicalTrials.gov Identifier: NCT00465556     History of Changes
Other Study ID Numbers: NR009093, 1R01NR009093-01A2
Study First Received: April 23, 2007
Last Updated: March 31, 2015
Health Authority: United States: Federal Government

ClinicalTrials.gov processed this record on April 30, 2015