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| Sponsors and Collaborators: |
Emory University Centers for Disease Control and Prevention National Institutes of Health (NIH) |
| Information provided by: | Emory University |
| ClinicalTrials.gov Identifier: | NCT00166062 |
Purpose
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.
| Condition | Intervention |
|
Intimate Partner Violence Perpetration |
Procedure: Screening patients for IPV and referring half of the victims (experimental group) to social work |
| Study Type: | Interventional |
| Study Design: | Educational/Counseling/Training, Randomized, Single Blind, Active Control, Single Group Assignment |
Eligibility
| Ages Eligible for Study: | 18 Years to 55 Years |
| Genders Eligible for Study: | Both |
Inclusion Criteria: Men and women age 18-55 who present to the emergency department waiting room during study hours
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Exclusion Criteria:
Contacts and Locations| Contact: Debra Houry | 4046163181 | dhoury@emory.edu |
| United States, Georgia | |||||
| Grady Memorial Hospital | Recruiting | ||||
| Atlanta, Georgia, United States, 30303 | |||||
| Contact: Debra Houry 404-616-3181 | |||||
| Principal Investigator: Debra Houry | |||||
| Principal Investigator: | Debra Houry | Emory University |
More Information
| Study ID Numbers: | R49/CCR423113-03 |
| First Received: | September 12, 2005 |
| Last Updated: | September 12, 2005 |
| ClinicalTrials.gov Identifier: | NCT00166062 |
| Health Authority: | United States: Institutional Review Board |
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