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

Testing Screening Formats for Indicator-Based and Universal Screening Measurements in the Identification of Woman Abuse.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00336297
Enrollment
2000
Registered
2006-06-13
Start date
2004-05-31
Completion date
2005-02-28
Last updated
2006-11-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Domestic Violence

Keywords

screening, screening methods, intimate partner violence

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.

Interventions

PROCEDUREWoman Abuse Screening Tool
PROCEDUREPartner Violence Screen
PROCEDUREComputerized screening
PROCEDUREFace to face screening
PROCEDUREWritten screening on forms

Sponsors

Ontario Women's Health Council
CollaboratorUNKNOWN
Hamilton Health Sciences Corporation
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 64 Years

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

Design outcomes

Primary

MeasureTime frame
disclosure rates for past year exposure to intimate partner violence

Secondary

MeasureTime frame
participant satisfaction with completing the instruments
missing data

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 11, 2026