Testing Methods of Screening for Woman Abuse in Health Ca... | NCT00336297

Studies
Testing Methods of Screening for Woman Abuse in Health Care Settings.

NCT00336297

Sponsor

Hamilton Health Sciences Corporation

Status

Completed

Last Update Posted

Nov 29, 2006Estimated

Enrollment

2,000

Phase

Not Applicable

Conditions

Domestic Violence

Interventions

Woman Abuse Screening Tool
Partner Violence Screen
Computerized screening
Face to face screening
Written screening on forms

Countries

Canada

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

Status Module

Record Verification Date

Feb 2005

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

May 2004

Primary Completion Date

Not provided

Completion Date

Feb 2005

First Submitted Date

Jun 9, 2006

First Submission Date that Met QC Criteria

Jun 9, 2006

First Posted Date

Jun 13, 2006Estimated

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

Nov 28, 2006

Last Update Posted Date

Nov 29, 2006Estimated

Name	Class
Ontario Women's Health Council	UNKNOWN

Description Module

Brief Summary

Recent reviews have identified the need for additional high quality exploratory and evaluative research to understand 1) the actual impact on all women of instituting mass screening procedures versus using indicator-based approaches to identifying woman abuse and 2) the extent to which early identification through screening -- either universal or indicator-based is effective in preventing or ameliorating important outcomes. This is a critical first step in developing a larger randomized controlled trial (RCT) which examines the effectiveness of screening in preventing woman abuse, improving quality of life and other associated outcomes. This study prepares for the RCT by testing the optimal method of administration for the two screening instruments that will be used in the RCT. The administration formats are: computer-based screen, paper and pencil screen and face-to-face screen. They study will also determine recruitment rates.

Detailed Description

Not provided

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

2,000

Arms/Interventions Module

Arm Groups

Not provided

Interventions

Name	Type	Description	Arm Group Labels	Other Names
Woman Abuse Screening Tool	Procedure
Partner Violence Screen	Procedure
Computerized screening	Procedure
Face to face screening	Procedure
Written screening on forms	Procedure

Outcomes Module

Primary Outcomes

Measure	Description	Time Frame
disclosure rates for past year exposure to intimate partner violence

Secondary Outcomes

Measure	Description	Time Frame
participant satisfaction with completing the instruments
missing data

Other Outcomes

Not provided

Eligibility Module

Eligibility Criteria

Inclusion Criteria:

Women aged 18-64 years
Patients at the health care site
Able to participate in English
Able to separate from accompanying person(s)

Exclusion Criteria:

Too ill to participate
Unable to separate from accompanying person(s)
Unable to speak, read, or write English

Accepts Healthy Volunteers

Not provided

Sex

Female

Sex/Gender Based

Not provided

Sex/Gender Description

Not provided

Minimum Age

18 Years

Maximum Age

64 Years

Standard Ages

Adult

Study Population

Not provided

Sampling Method

Not provided

Contacts/Locations Module

Central Contacts

Not provided

Overall Officials

Name	Affiliation	Role
Harriet L MacMillan, MD, MSc	McMaster University	Principal Investigator

Locations

Facility	Status	City	State	ZIP	Country	Contacts
Cambridge Memorial Hospital - Emergency Department		Cambridge	Ontario		Canada
Carlisle Medical Centre

References Module

Citations

PubMed Identifier	Type	Citation	Retractions
16882959	Result	MacMillan HL, Wathen CN, Jamieson E, Boyle M, McNutt LA, Worster A, Lent B, Webb M; McMaster Violence Against Women Research Group. Approaches to screening for intimate partner violence in health care settings: a randomized trial. JAMA. 2006 Aug 2;296(5):530-6. doi: 10.1001/jama.296.5.530.