NCT00166062

Completed

Safety and Effectiveness of Computer Screening for Intimate ...

Emory University Source

Other study identifiers

Sponsor study identifier

0304-2003

Secondary identifiers

R49/CCR423113-03

OTHER · Other

Study Type

interventional

Reported enrollment (type unavailable)

N/A

Locations

1 country

Sites

1

Timeline

Study Start

January 2004

Date type not reported

This date has not been verified as actual or estimated.

Primary Completion

December 2006

Actual (reported)

Study Completion

December 2007

Actual (reported)

Brief 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.

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: completed
Reported enrollment (type unavailable): Not reported
Study completion date: December 2007
Actual (reported)
Listed locations: 1 countries · 1 sites

Trial Relationships

Click on a node to explore related trials.

Some registry-reported names shown below are not yet linked in this graph.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

Study Start
January 2004
Date type not reported
This date has not been verified as actual or estimated.
First Submitted
September 12, 2005
Actual (reported)
First Posted
September 14, 2005
Actual (reported)
Primary Completion
December 2006
Actual (reported)
Study Completion
December 2007
Actual (reported)

Last Updated: September 20, 2013
Status Verified: September 2013
Last Update Submitted: September 19, 2013

Conditions

Domestic Violence Perpetration

Keywords

intimate partner violenceperpetration

Outcome Measures

Primary Outcomes (2)

Adverse events in the ED
Increased violence at follow up

Interventions

Screening patients for IPVProcedure

Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.

Eligibility Criteria

Age18 Years - 55 Years

Sexall

Age GroupsAdult (18-64)

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Emory University
Otherlead
National Institutes of Health (NIH)
NIHcollaborator
Centers for Disease Control and Prevention

Study Sites (1)

Grady Memorial Hospital

Atlanta, Georgia, 30303, United States

MeSH Terms

Interventions

Poliovirus Vaccine, Inactivated

Intervention Hierarchy (Ancestors)

Vaccines, InactivatedVaccinesBiological ProductsComplex MixturesPoliovirus VaccinesViral Vaccines

Study Officials

Debra Houry
Emory University
PRINCIPAL INVESTIGATOR

Study Design

Study Type: interventional
Phase: not applicable
Allocation: RANDOMIZED
Masking: SINGLE
Intervention Model: SINGLE GROUP
Sponsor Type: OTHER
Responsible Party: PRINCIPAL INVESTIGATOR
PI Title: Principal Investigator

Study Record Dates

First Submitted

September 12, 2005

First Posted

September 14, 2005

Study Start

January 2004

Date type not reported

This date has not been verified as actual or estimated.

Primary Completion

December 2006

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Not ApplicableTerminated

US federal agencycollaborator

Actual (reported)

Study Completion

December 2007

Actual (reported)

Last Updated

September 20, 2013

Record last verified: 2013-09

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT00166062
Data provider: ClinicalTrials.gov
Source updated: 2013-09-20
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:35:26 UTC

Locations

US(1)

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

First Submitted

First Posted

Primary Completion

Study Completion

Conditions

Keywords

Outcome Measures

Primary Outcomes (2)

Interventions

Eligibility Criteria

You may not qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Interventions

Intervention Hierarchy (Ancestors)

Study Officials

Study Design

Study Record Dates

Source record

Locations