Brief Intervention to Reduce Drinking Among Batterers

This study is ongoing, but not recruiting participants.
Sponsor:
Collaborators:
Butler Hospital
Information provided by (Responsible Party):
The University of Tennessee Knoxville
ClinicalTrials.gov Identifier:
NCT00539955
First received: September 25, 2007
Last updated: December 17, 2012
Last verified: December 2012
  Purpose

The goal of this project is to examine whether, relative to standard care, violence and alcohol use outcomes can be improved by a brief, motivationally based adjunct alcohol treatment for men enrolled in batterer intervention programs. We hypothesize that men randomized to also receive the brief alcohol intervention will have better partner violence and alcohol use outcomes than men who are randomized to the batterer intervention program alone.


Condition Intervention Phase
Intimate Partner Violence
Alcohol Use
Behavioral: Standard Batterer Intervention
Behavioral: Brief Alcohol Intervention
Phase 2

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Brief Intervention to Reduce Drinking Among Batterers

Resource links provided by NLM:


Further study details as provided by The University of Tennessee Knoxville:

Primary Outcome Measures:
  • Intimate partner violence Substance use [ Time Frame: one year ] [ Designated as safety issue: No ]

Estimated Enrollment: 253
Study Start Date: July 2003
Estimated Study Completion Date: December 2012
Estimated Primary Completion Date: December 2012 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
1
Standard 40 hour state-mandated batterer intervention
Behavioral: Standard Batterer Intervention
Standard state-mandated batterer intervention program (40 hours)
2
Brief alcohol intervention combined with standard batterer intervention
Behavioral: Brief Alcohol Intervention
Brief alcohol intervention combined with state mandated batterer intervention program

  Eligibility

Genders Eligible for Study:   Male
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Participation in a batterer intervention program
  • Hazardous drinking
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00539955

Locations
United States, Rhode Island
Butler Hospital
Providence, Rhode Island, United States, 02906
Sponsors and Collaborators
The University of Tennessee Knoxville
Butler Hospital
Investigators
Principal Investigator: Gregory L. Stuart, PhD University of Tennessee-Knoxville & Butler Hospital
Principal Investigator: David Strong, PhD Butler Hospital
  More Information

No publications provided

Responsible Party: The University of Tennessee Knoxville
ClinicalTrials.gov Identifier: NCT00539955     History of Changes
Other Study ID Numbers: NIAAA-STU_014193_0111-001-M, R01AA014193
Study First Received: September 25, 2007
Last Updated: December 17, 2012
Health Authority: United States: Federal Government

Keywords provided by The University of Tennessee Knoxville:
intimate partner violence
alcohol use
substance use

Additional relevant MeSH terms:
Alcohol Drinking
Drinking Behavior
Ethanol
Anti-Infective Agents, Local
Anti-Infective Agents
Therapeutic Uses
Pharmacologic Actions
Central Nervous System Depressants
Physiological Effects of Drugs
Central Nervous System Agents

ClinicalTrials.gov processed this record on July 28, 2014