Safety and Effectiveness of Computer Screening for Intima... | NCT00166062

Studies
Safety and Effectiveness of Computer Screening for Intimate Partner Violence

NCT00166062

Sponsor

Emory University

Status

Completed

Last Update Posted

Sep 20, 2013Estimated

Enrollment

Not provided

Phase

Not Applicable

Conditions

Domestic Violence
Perpetration

Interventions

Screening patients for IPV

Countries

United States

Protocol Section

Identification Module Status Module Sponsor/Collaborators Module Oversight Module Description Module Conditions Module Design Module Arms/Interventions Module Outcomes Module Eligibility Module Contacts/Locations Module References Module IPD Sharing Statement Module

Results Section

Participant Flow Module Baseline Characteristics Module Outcome Measures Module Adverse Events Module More Info Module

Annotation Section

Annotation Module

Document Section

Large Document Module

Derived Section

Miscellaneous Info Module Condition Browse Module Intervention Browse Module

Protocol Section

Identification Module

NCT ID

Results Section

No data available

No data is available for this block.

Annotation Section

No data available

No data is available for this block.

Document Section

No data available

No data is available for this block.

Derived Section

Miscellaneous Info Module

Version Holder

ID	Type	Description	Link
R49/CCR423113-03	Other Identifier	Other

Status Module

Record Verification Date

Sep 2013

Overall Recruitment Status or Expanded Access Status

Completed

Last Known Status

Not provided

Delayed Posting

Not provided

Why Stopped

Not provided

Expanded Access Info

Start Date

Jan 2004

Primary Completion Date

Dec 2006Actual

Completion Date

Dec 2007Actual

First Submitted Date

Sep 12, 2005

First Submission Date that Met QC Criteria

Sep 12, 2005

First Posted Date

Sep 14, 2005Estimated

Results Waived

Not provided

Results First Submitted Date

Not provided

Results First Submitted that Met QC Criteria

Not provided

Results First Posted Date

Not provided

Certification/Extension (aka Delayed Results) First Submitted Date

Not provided

Certification/Extension First Submitted that Passed QC Review

Not provided

Certification/Extension First Posted Date

Not provided

Last Update Submitted Date

Sep 19, 2013

Last Update Posted Date

Sep 20, 2013Estimated

Sponsor/Collaborators Module

Responsible Party, by Official Title

Debra Houry, MD, MPH, Principal Investigator, Emory UniversityPrincipal Investigator

Lead Sponsor

Emory UniversityOTHER

Collaborators

Name	Class
Centers for Disease Control and Prevention	FED
National Institutes of Health (NIH)	NIH

Description Module

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.

Detailed 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.

Design Module

Study Type

Interventional

Number of References to an Expanded Access Study

Not provided

Expanded Access Types

Not provided

Patient Registry

Not provided

Target Follow-Up Duration

Not provided

Phases

Not Applicable

Interventional Study Design

Allocation

Biospecimen

No data available

No data is available for this block.

Enrollment

Not provided

Name	Type	Description	Arm Group Labels	Other Names
Screening patients for IPV	Procedure

Outcomes Module

Primary Outcomes

Measure	Description	Time Frame
Adverse events in the ED
Increased violence at follow up

Secondary Outcomes

Not provided

Other Outcomes

Not provided

Eligibility Module

Eligibility Criteria

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

Accepts Healthy Volunteers

Not provided

Sex

All

Sex/Gender Based

Not provided

Sex/Gender Description

Not provided

Minimum Age

18 Years

Maximum Age

55 Years

Standard Ages

Adult

Study Population

Not provided

Sampling Method

Not provided

Contacts/Locations Module

Central Contacts

Not provided

Overall Officials

Name	Affiliation	Role
Debra Houry	Emory University	Principal Investigator

Locations

Facility	Status	City	State	ZIP	Country	Contacts
Grady Memorial Hospital		Atlanta	Georgia	30303	United States

Intervention Browse Module

MeSH Terms

ID	Term
D011054	Poliovirus Vaccine, Inactivated

Ancestor Terms

ID	Term
D015164	Vaccines, Inactivated
D014612	Vaccines
D001688	Biological Products
D045424	Complex Mixtures

Browse Leaves

Not provided

Browse Branches

Not provided