Domestic Violence Clinical Trial
Verified date | September 2013 |
Source | Emory University |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Interventional |
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.
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 |
Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Single Blind
Country | Name | City | State |
---|---|---|---|
United States | Grady Memorial Hospital | Atlanta | Georgia |
Lead Sponsor | Collaborator |
---|---|
Emory University | Centers for Disease Control and Prevention, National Institutes of Health (NIH) |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Adverse events in the ED | |||
Primary | Increased violence at follow up |
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