Domestic Violence Enhanced Home Visitation Program (DOVE)
The recruitment status of this study is unknown because the information has not been verified recently.
Verified February 2010 by Johns Hopkins University.
Recruitment status was Recruiting
Recruitment status was Recruiting
Sponsor:
Johns Hopkins University
Collaborator:
Information provided by:
Johns Hopkins University
ClinicalTrials.gov Identifier:
NCT00465556
First received: April 23, 2007
Last updated: February 19, 2010
Last verified: February 2010
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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 |
|---|---|---|
|
Intimate Partner Violence |
Behavioral: Public Health Nurse Home Visit Behavioral: Intimate Partner Violence (IPV) Protocol |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized 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 ]
| Estimated Enrollment: | 360 |
| Study Start Date: | February 2006 |
| Estimated Study Completion Date: | November 2010 |
| Estimated 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
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00465556
Contacts
| Contact: Phyllis Sharps, PhD, RN, FAAN | 410-614-5312 | psharps@son.jhmi.edu |
Locations
| United States, Maryland | |
| Baltimore City Health Department | Recruiting |
| Baltimore, Maryland, United States, 21205 | |
| Contact: Phyllis Sharps, PhD, RN, FAAN 410-614-5312 psharps@son.jhmi.edu | |
| Principal Investigator: Phyllis Sharps, PhD, RN, FAAN | |
| 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 | Recruiting |
| Columbia, Missouri, United States, 65211 | |
| Contact: Linda Bullock, PhD, RN, FAAN 573-882-0234 | |
| Sub-Investigator: Linda Bullock, PhD, RN, FAAN | |
Sponsors and Collaborators
Johns Hopkins University
Investigators
| Principal Investigator: | Phyllis Sharps, PhD, RN, FAAN | Johns Hopkins University |
More Information
No publications provided
| Responsible Party: | Phyllis W. Sharps, PhD, RN, CNE, FAAN, Professor and Department Chair for Community Public Health, Johns Hopkins University School of Nursing |
| ClinicalTrials.gov Identifier: | NCT00465556 History of Changes |
| Other Study ID Numbers: | NR009093, 1R01NR009093-01A2, 1 R01 NR009093-01A2 |
| Study First Received: | April 23, 2007 |
| Last Updated: | February 19, 2010 |
| Health Authority: | United States: Federal Government |
ClinicalTrials.gov processed this record on June 18, 2013