Women Initiating New Goals of Safety

NCT01788579 | Completed Phase 1

• 2 other identifiers: AAAI2851R34DA031325
• Study Type: interventional
• Target: 209
• Locations: 1 country
• Sites: 3

Brief Summary

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. 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. 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. 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.
4. 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.

Conditions

Intimate Partner Violence

Keywords

Intimate Partner Violence (IPV); Drug Abuse; Criminal Justice

Outcome Measures

Primary Outcomes (2)

• 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

• Utilization of IPV services

  Up to 3 months from baseline

Study Arms (2)

Multimedia WINGS

EXPERIMENTAL

A one-hour session of a self-paced multimedia IPV screening, brief intervention and referral service delivered on a computer.

Behavioral: Multi-media WINGS

Caseworker Delivered WINGS

ACTIVE COMPARATOR

A one-hour session of IPV screening, brief intervention and referral service delivered by a case manager.

Behavioral: Caseworker Delivered WINGS

Interventions

Multi-media WINGS BEHAVIORAL

This one-hour computerized multimedia IPV prevention service tool features the same activities as the comparison condition, but these core elements are translated into interactive tools and culturally tailored video vignettes designed to enhance learning and provide individualized feedback. Thus, the multimedia service tool acts as a roadmap for this service session, prompting participants through the IPV screening, providing psycho-educational content on IPV and how IPV may interact with their substance misuse, providing individualized feedback on their IPV risks based on the screening e, creating a safety plan, defining relationship safety goals and identifying IPV-related service needs, and generating a personal plan for accessing services and contacting agency representative.

Multimedia WINGS

Caseworker Delivered WINGS BEHAVIORAL

The content for the comparison service condition incorporates the core elements of best practices for IPV screening, safety planning and referrals recommended by the American Medical Association and previous service research. It also contains brief psycho-educational content on recognizing IPV and how IPV may contribute to drug use and recidivism drawn from previous interventions and demonstrated to have promising effects in reducing rates of both IPV and drug use.

Caseworker Delivered WINGS

Eligibility Criteria

• Age: 18 Years+
• Sex: female
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• 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

You may not qualify if:

• 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.

Sponsors & Collaborators

• Columbia University: lead
• National Institute on Drug Abuse (NIDA): collaborator

Study Sites (3)

Brooklyn Probation

Brooklyn, New York, 11201, United States

Location

Bronx Community Solutions

New York, New York, 10018, United States

Location

Bronx Probation

New York, New York, 10018, United States

Location

MeSH Terms

Conditions

Substance-Related Disorders

Condition Hierarchy (Ancestors)

Chemically-Induced Disorders; Mental Disorders

Study Officials

• Louisa Gilbert, PhD

  Columbia University

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: SINGLE
• Who Masked: PARTICIPANT
• Purpose: SCREENING
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Co-Director, Social Intervention Group, Global Health Research Center of Central Asia

Study Record Dates

• First Submitted: February 7, 2013
• First Posted: February 11, 2013
• Study Start: March 1, 2012
• Primary Completion: April 1, 2013
• Study Completion: April 1, 2013
• Last Updated: February 27, 2014

Record last verified: 2014-02

Locations

US (3)