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NCT00166062 Clinical Trial

Safety and Effectiveness of Computer Screening for Intimate Partner Violence

Domestic Violence Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00166062
Other study ID # 0304-2003
Secondary ID R49/CCR423113-03
Status Completed
Phase N/A
First received September 12, 2005
Last updated September 19, 2013
Start date January 2004
Est. completion date December 2007

Study information
Verified date September 2013
Source Emory University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this study is to see if using a computer kiosk to screen men and women for intimate partner violence victimization and perpetration is safe and effective. We hypothesize that screening will not result in any adverse events.

Description:

All eligible ER patients will be screened during study times for IPV victimization and perpetration. All victims will be followed at 1 week and 3 months to determine any adverse outcomes. Perpetrators will only be followed in the ED for adverse outcomes after screening. All patients who disclose IPV victimization or perpetration will get a list of community resources. Victims will be asked at follow up what resources they used.

Recruitment information / eligibility
Status Completed
Enrollment 0
Est. completion date December 2007
Est. primary completion date December 2006
Accepts healthy volunteers
Gender Both
Age group 18 Years to 55 Years
Eligibility Inclusion Criteria: Men and women age 18-55 who present to the emergency department waiting room during study hours

Exclusion Criteria:

- Acutely intoxicated, psychotic, unable to read, not English speaking

Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Single Blind

Related Conditions & MeSH terms

Intervention

Procedure:
• Screening patients for IPV

Locations
Country Name City State
United States Grady Memorial Hospital Atlanta Georgia

Sponsors (3)
Lead Sponsor Collaborator
Emory University Centers for Disease Control and Prevention, National Institutes of Health (NIH)

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Adverse events in the ED
Primary Increased violence at follow up
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