- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02021838
Evaluation of the Office on Violence Against Women's Domestic Violence Homicide Prevention Demonstrative Initiative (DVHPDI)
Evaluation of the Domestic Violence Homicide Prevention Initiative
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Process Evaluation: The process evaluation will assess: 1) the training and technical assistance provided to sites; 2) the implementation of the models in the communities; and 3) characteristics of the service delivery systems.
Technical Assistance Providers will document the training and technical assistance (TTA) they provide to the sites.
Sites will be asked to identify key stakeholders to participate in interviews before the implementation begins and then two additional times during the demonstration phase. Key informant interviews will assess: recipient's perception of the training and technical assistance; model fidelity; model implementation (including model penetration, barriers and facilitators to implementation); and, perceptions of model impact. In addition to key informant interviews administrative data will be gathered to assess aspects of model implementation and systematic observations of law enforcement initiated screens will be conducted by a member of the evaluation team who will join patrol officers for "ride-alongs".
Impact Evaluation: The impact evaluation will assess changes in: 1) collaboration among service sectors; 2) supervision and sanctions for offenders; 3) recidivism and re-victimization; 4) victim reported feelings of safety; 5) utilization of resources; and 6) nature of safety planning.
System Collaboration will be assessed through a web-based survey completed at three time points by key stakeholders representing all potential partners in the community. Social network analysis will provide a visual depiction of how the network changes over time.
Victim Interviews will be conducted to determine the impact of involvement in the model program on their safety and wellbeing. Victims will be interviewed at three time points and will be asked about: prior and recent contact with law enforcement, domestic violence service providers or other providers; awareness of resources to address IPV; their safety and fear of their partner; coping strategies utilized; social support; financial resources; willingness to utilize criminal justice system and domestic violence service providers; both their and offenders behavior, beliefs and attitudes; self-reported mental health and substance abuse; their report of offenders substance abuse; and demographic information.
Administrative Data will be utilized to examine the breadth of the model implementation; the impact of the model programs on criminal justice processes; and whether there is a connection between the extent of post-risk assessment sanctions and services and the pattern of newly recorded incidents between the victim and offender. The evaluation will compare processing and outcomes across cases that are in many ways similar except that some cases were determined to be high risk and a risk assessment was completed and others where a risk assessment was not conducted. To facilitate these comparisons, the evaluation team will build a comprehensive database that will depict the "life-history" of each victim and offender dyad.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Connecticut
-
New Haven, Connecticut, United States, 06511
- Yale University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
The demonstration sites are:
California North Carolina Ohio Illinois Michigan Tennessee
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
California
Lethality Assessment Program
|
Law enforcement officers conduct risk screen of domestic violence victims, if high risk victims are referred to domestic violence services.
Other Names:
|
|
North Carolina
Lethality Assessment Program
|
Law enforcement officers conduct risk screen of domestic violence victims, if high risk victims are referred to domestic violence services.
Other Names:
|
|
Ohio
Domestic Violence High Risk Team
|
Law enforcement officers conduct risk screen of domestic violence victims, if high risk victims are referred to domestic violence services and a team who monitors the clinical and criminal justice progress.
Other Names:
|
|
Illinois
Lethality Assessment Program
|
Law enforcement officers conduct risk screen of domestic violence victims, if high risk victims are referred to domestic violence services.
Other Names:
|
|
Michigan
Lethality Assessment Program
|
Law enforcement officers conduct risk screen of domestic violence victims, if high risk victims are referred to domestic violence services.
Other Names:
|
|
Tennessee
Lethality Assessment Program
|
Law enforcement officers conduct risk screen of domestic violence victims, if high risk victims are referred to domestic violence services.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Decreased frequency of re-assault
Time Frame: up to 3 years
|
Decrease in harassment, assault, injury, homicide/mortality
|
up to 3 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Increased collaboration between network partners
Time Frame: up to 3 years
|
Increased information sharing, case planning, coordinated response
|
up to 3 years
|
|
Increased awareness of and utilization of resources for victims
Time Frame: Up to 3 years
|
Increased awareness of and utilization of community resources
|
Up to 3 years
|
|
Increased safety planning
Time Frame: Up to 3 years
|
Increased safety planning at the time of police intervention
|
Up to 3 years
|
|
Increased victim reported safety
Time Frame: Up to 3 years
|
Victim reported changes in perceptions of safety
|
Up to 3 years
|
|
Increased sanctions for offender
Time Frame: Up to 3 years
|
Sanctions such as pre-trial containment, cases to trial, adjudications, containment post-adjudication
|
Up to 3 years
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Joy S Kaufman, PhD, Yale University
- Study Director: Christopher Maxwell, PhD, Michigan State University
- Study Director: Tami Sullivan, PhD, Yale University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 1311013010
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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