Intimate Partner Violence Clinical Trial
— WINGSOfficial title:
Project WINGS: Women Initiating New Goals of Safety
Verified date | February 2014 |
Source | Columbia University |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Interventional |
This study aims to conduct a randomized controlled trial that will test the feasibility and
preliminary effect of a multimedia version of a computerized multimedia intimate partner
violence (IPV) prevention service tool designed to increase identification of IPV
victimization and to improve linkages to IPV-related services among female offenders under
court supervision or probation, compared to a non-media version of the same IPV screening,
brief intervention and referral service delivered by a case manager. The study addresses the
following: Primary study aims
1. To design and beta-test a Computerized Multimedia IPV Screening, Brief Intervention and
Referral Service tool for female offenders under court supervision or probation.
2. To obtain preliminary estimates of the effects of the Computerized Multimedia versus
the Case Manager IPV service conditions on identification of different types of IPV
during the service session and on access to and utilization of IPV services over the
three-month follow-up period.
3. To examine and enhance the feasibility (recruitment, enrollment, fidelity of service
delivery, client satisfaction, safety, and retention) for a future larger scale R01
study.
Secondary study aim
4. To obtain estimates of the effects of the Computerized Multimedia versus the Case
Manager IPV service conditions on recidivism, adherence to drug treatment (e.g.,
attendance, completion) and abstinence of substance use over the follow-up period,
controlling for baseline outcomes.
Status | Completed |
Enrollment | 209 |
Est. completion date | April 2013 |
Est. primary completion date | April 2013 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - She is 18 or older - She is currently court supervision at Bronx Community Solutions or a drug treatment court or she is currently on probation. - She reports using any illicit drug or drinking 4 or more alcoholic drinks in a 6-hour period in the past 90 days or she has been in alcohol or drug treatment in the past 6 months OR if she report attending any drug or alcohol treatment in the past 6 months. - She reports having had an ongoing intimate, dating or sexual relationship with a male or female partner that lasted 3 or more months in the past year. - She lives within a 90-minute commute of 125th and Broadway Exclusion Criteria: - Ability to speak and understand English is not sufficient to participate in assessments or intervention sessions. - Inability to complete informed consent process due to a psychiatric or cognitive impairment. - The participant is unwilling or unable to commit to completing all the activities in the study. |
Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Screening
Country | Name | City | State |
---|---|---|---|
United States | Brooklyn Probation | Brooklyn | New York |
United States | Bronx Community Solutions | New York City | New York |
United States | Bronx Probation | New York City | New York |
Lead Sponsor | Collaborator |
---|---|
Columbia University | National Institute on Drug Abuse (NIDA) |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Number of subjects with identified Intimate Partner Violence (IPV) | If participants score a 20 or higher on the Women's Experience with Battering (WEB) survey, if they indicate yes to any of the Partner Abuse Interview or Partner Violence Screen (PVS), the tool will inform participants that they are at risk of IPV. If participants indicate yes to any severe IPV items, the tool will indicate that they are at risk of life-threatening IPV and should consider taking immediate steps to reduce their risks for IPV. All other participants will be informed that based on the answers, they do not appear to be at risk for IPV at present, but that they may learn strategies to prevent IPV in the session. | Up to 3 months from baseline | No |
Primary | Utilization of IPV services | Up to 3 months from baseline | No |
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