Brief Intervention for Alcohol Use Among Injured Patients

Sponsor
University of California, Davis (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT00278785
Collaborator
California Office of Traffic Safety (Other)
830
1
2
250.8
3.3

Study Details

Study Description

Brief Summary

The underlying hypothesis that providing brief interventions to individuals who engage in potentially harmful patterns of alcohol use will alter their drinking behavior and therefore avoid negative consequences. Specifically, this study aims to determine if brief interventions will:

  1. Reduce the number of re-admissions and deaths due to injuries associated with alcohol consumption

  2. Reduce the number of driving under the influence (DUI) arrests

  3. Reduce harmful drinking behavior

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Brief Motivational Interview
N/A

Detailed Description

Alcohol use is the most common underlying cause of injuries in the United States. There is a growing body of literature suggesting that brief interventions (BI), in the form of a short (10-60 minute) counseling session, may decrease alcohol consumption and its harmful consequences. In contrast to the abundant literature on the effectiveness of BI in the outpatient setting, only 3 randomized controlled trials have been performed an adults specifically in the setting of acute trauma, and have had inconclusive results. All three studies used highly trained persons to perform the BI, and all were greater than 30 minutes in duration, a situation that may not necessarily reflect the practicalities of routine medical care. This raises the question of whether the benefits seen in these studies reflect the expertise of a small number of individuals or whether the effects correlate with the amount of time spent with the patient. Highly trained personnel and time are valuable commodities in a busy trauma center and may not be feasible given the competing clinical demands. We propose to investigate whether BI are effective in a setting that is more likely to reflect "real world" of clinical medicine rather than an idealized setting, utilizing trauma nurse practitioners to perform brief (5-10 minute) interviews.

We will identify all patients admitted with trauma who test positive on a blood alcohol test. These patients will be consented and randomized to either a brief intervention group, or a standard medical care group. All patients will receive an AUDIT questionnaire to identify patterns of drinking behavior and an alcohol information pamphlet. After discharge, patients will be telephoned at 1,6, and 12 months. The first 2 contacts will be to see how the patient is doing and to verify the contact information. The AUDIT questionnaire will be re-administered during the 12 month interview.

Study Design

Study Type:
Interventional
Actual Enrollment :
830 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
Brief Intervention for Alcohol Use Among Injured Patients: A Prospective, Randomized Trial
Study Start Date :
Mar 1, 2006
Anticipated Primary Completion Date :
Jan 24, 2027
Anticipated Study Completion Date :
Jan 24, 2027

Arms and Interventions

Arm Intervention/Treatment
No Intervention: 1

Control group to receive informational pamphlet on alcohol use and list of self referral agencies

Experimental: 2

Intervention group receives pamphlet on alcohol and self referral information in addition to brief motivational interview

Behavioral: Brief Motivational Interview
10-20 minute brief motivational interview
Other Names:
  • Brief intervention
  • Motivational interview
  • Outcome Measures

    Primary Outcome Measures

    1. Hospital re-admissions [2 years]

      number of hospital re-admissions

    Secondary Outcome Measures

    1. 12 month AUDIT Results [12 months]

      Score on self administered questionnaire

    2. Moving violations/DUI [2 years]

      number of moving violations/DUI

    3. Self referral for counselling/treatment [12 months]

      number of self referrals for counseling/treatment

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • =18 yrs old

    • English or Spanish Speaking

    • Mentally and physically able to provide consent and participate in the intervention

    • Admission to the trauma ward or ICU

    Exclusion Criteria:
    • <18 yrs old

    • Non-English or Non-Spanish Speaking

    • Severe Psychiatric illness

    • incarcerated

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of California, Davis, Medical Center Sacramento California United States 95817

    Sponsors and Collaborators

    • University of California, Davis
    • California Office of Traffic Safety

    Investigators

    • Principal Investigator: Garth H. Utter, MD, MSc, University of California, Davis

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    University of California, Davis
    ClinicalTrials.gov Identifier:
    NCT00278785
    Other Study ID Numbers:
    • 237217
    • Office of Traffic Safety
    • Grant Number AL0584
    First Posted:
    Jan 18, 2006
    Last Update Posted:
    Jun 24, 2021
    Last Verified:
    Jun 1, 2021
    Keywords provided by University of California, Davis
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jun 24, 2021