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Alcohol Screening, Brief Intervention, and Referral to Treatment in a Military Treatment Facility

Primary Purpose

Alcohol Dependency

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
SBIRT
Sponsored by
San Diego State University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Alcohol Dependency focused on measuring Alcohol Use, SBIRT, Military, Health Behavior, Emergency Room, Health Promotion, Formative Research, Randomized Trial

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • 18 or Older
  • Active Duty
  • Off Duty
  • Telephone Number for Follow-up
  • Healthy Enough to Participate
  • Positive Screen for Risky Drinking

Exclusion Criteria:

  • Under 18
  • Non-Military
  • On Duty
  • Low Level Drinking

Sites / Locations

  • Naval Medical Center San Diego

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Active Comparator

Arm Label

Usual Care

SBIRT

Arm Description

Those participants assigned to the usual care control group will be given a brochure on safe drinking limits, will be reminded of the 6-month follow-up, and thanked for their time.

Those assigned to the SBIRT intervention group will receive 1 of 3 tracks: Brief Intervention (BI) for At Risk Individuals (scores lower than 15) - Brief motivational intervention with feedback related to their use and change strategies. Brief Treatment (BT) for High Risk Individuals (scores of 16-19) - Brief Intervention on site and be offered 6 individual confidential sessions with a civilian Brief Treatment Counselor over the phone. Referral to Treatment (RT) for Severe Risk Individuals (scores of 20-40) - Brief Intervention on site and will be given a list of services where they may self-refer for further assessment and support.

Outcomes

Primary Outcome Measures

Alcohol Use Disorders Identification Test (AUDIT) Total
The primary outcome measure will come from the participant's total score on the AUDIT. Scores on the AUDIT range from 0 to 40 with higher numbers indicating greater problematic alcohol use. Mean AUDIT scores at follow-up will be compared between arms.

Secondary Outcome Measures

AUDIT-C or Drinkers Index
The drinkers index consists of a summary of the first three AUDIT items which represents a combination of quantity, usual frequency, and frequency of heavy drinking. The AUDIT-C can range from 0 to 12 with 12 representing higher levels of drinking quantity and frequency.
Controlled Drinking Self-Efficacy Scale (CDSES)
The 20-item Controlled Drinking Self-Efficacy Scale (CDSES), is a reliable, valid, easy-to-administer scale that assesses confidence to reduce overall consumption and frequency of drinking. Items range from 0% to 100% with 100% indicating more confidence to engage in controlled drinking. The CDSES was administered at both baseline and follow-up to assess changes in this presumed mediating attitude.
Readiness to Change Scale
A readiness to change alcohol use measure (ranging from 1 - not ready to change, to 4 - very ready) was assessed at baseline and follow-up for all participants. Because motivation and readiness to change are hallmark elements of the SBIRT approach and are thought to be integral to behavior change, these constructs will be measured to assess the degree to which they change in the two groups. Some individuals may not abstain or reduce their use over time, but there may be an improvement in their readiness to change.

Full Information

First Posted
August 26, 2014
Last Updated
August 21, 2020
Sponsor
San Diego State University
Collaborators
United States Naval Medical Center, San Diego
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1. Study Identification

Unique Protocol Identification Number
NCT02228967
Brief Title
Alcohol Screening, Brief Intervention, and Referral to Treatment in a Military Treatment Facility
Official Title
Feasibility and Pilot Testing of SBI to Reduce Alcohol Misuse Among Active Duty Members in a Military ER Setting
Study Type
Interventional

2. Study Status

Record Verification Date
August 2020
Overall Recruitment Status
Completed
Study Start Date
August 2015 (Actual)
Primary Completion Date
October 2016 (Actual)
Study Completion Date
August 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
San Diego State University
Collaborators
United States Naval Medical Center, San Diego

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
An alcohol Screening, Brief Intervention and Referral to Treatment (SBIRT) approach will be adapted for use in a large military hospital setting, and then pilot tested in a military emergency department (ED) to assess its potential for effectiveness and for further testing in a large-scale trial. SBIRT is an "opportunistic" approach whereby all adult patients in the ED are screened by Health Educators for their alcohol use, and then, taking advantage of a "teachable moment," are delivered a brief, motivational intervention matched to their level of risk. The feasibility/formative research activities in the first phase (Phase I) of the study are not summative research, and therefore, do not lend themselves to testable hypotheses. Hypotheses with regard to the pilot randomized trial in Phase II are as follows: Participants in the SBIRT intervention will show relatively greater reductions over a six month period (or less increase) than the brochure/usual care control group in the prevalence of past-month heavy drinking, frequency of heavy drinking, past week number of drinks, and the AUDIT-based drinkers' index. Alcohol use-related motivation/readiness to change and controlled drinking self-efficacy will show greater change in the SBIRT intervention group relative to the brochure/usual care control group. In addition, exploratory analyses will examine the following: Sociodemographic/military variables (e.g., age, race/ethnicity, gender, branch of service, officer/enlisted status, PTS) and social-psychological factors (e.g., baseline readiness to change, self efficacy) will mediate or moderate changes in alcohol misuse.
Detailed Description
Deployment frequency and duration and combat exposure are implicated as risk factors for alcohol misuse and PTSD among military personnel. During the past 10 years, Department of Defense healthcare systems have observed steep increases in mental health and substance use services among personnel demobilizing from these conflicts. Although the alcohol Screening, Brief Intervention and Referral to Treatment (SBIRT) approach has shown promise as a low-cost, effective strategy for reducing alcohol use in civilians many of whom are risky drinkers but not yet dependent, it has not been adapted or tested in military health care settings for active duty personnel. This 2.5 year civilian-military collaborative study is highly responsive to exploring solutions to this emerging issue. The specific objectives for the overall project are given below. Objective 1: Feasibility and Acceptability Determine how the SBIRT intervention can be integrated into standard military emergency department (ED) operations by conducting record review and observation of the ED. Develop and test the acceptability and usability (for both ED staff and potential participants) of the SBIRT approach by conducting focus groups with active duty personnel and garnering input from ED staff. Develop an implementation/operations protocol for delivering SBIRT in the ED. Objective 2: Adaptation Apply a translational research approach to adapt SBIRT implementation in military settings and populations by using information from focus groups and input from ED staff. Adapt the content of the SBIRT intervention to be relevant for military personnel, including language and images for counseling and materials using information from focus groups and input from ED staff. Objective 3: Pilot Trial Using a two group repeated measures design, assess the impact of SBIRT using standardized alcohol use measures to assess its potential for effectiveness with active duty military personnel in an ED setting. Specific methodologies include: Apply a randomization method in the ED to assign active duty participants to experimental condition. Implement the SBIRT intervention in the ED for those assigned to the intervention arm. Implement a process for obtaining follow-up data with this mobile population. Assess presumed mediators (e.g., readiness/motivation to change and self-efficacy) and moderators (e.g., PTSD status, gender) of alcohol misuse change.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Alcohol Dependency
Keywords
Alcohol Use, SBIRT, Military, Health Behavior, Emergency Room, Health Promotion, Formative Research, Randomized Trial

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
791 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Usual Care
Arm Type
No Intervention
Arm Description
Those participants assigned to the usual care control group will be given a brochure on safe drinking limits, will be reminded of the 6-month follow-up, and thanked for their time.
Arm Title
SBIRT
Arm Type
Active Comparator
Arm Description
Those assigned to the SBIRT intervention group will receive 1 of 3 tracks: Brief Intervention (BI) for At Risk Individuals (scores lower than 15) - Brief motivational intervention with feedback related to their use and change strategies. Brief Treatment (BT) for High Risk Individuals (scores of 16-19) - Brief Intervention on site and be offered 6 individual confidential sessions with a civilian Brief Treatment Counselor over the phone. Referral to Treatment (RT) for Severe Risk Individuals (scores of 20-40) - Brief Intervention on site and will be given a list of services where they may self-refer for further assessment and support.
Intervention Type
Behavioral
Intervention Name(s)
SBIRT
Other Intervention Name(s)
Screening, Brief Intervention, Brief Treatment, Referral to Treatment, Motivational Interviewing
Intervention Description
SBIRT is an "opportunistic" approach whereby patients are screened by Health Educators for their alcohol use, and then, taking advantage of a "teachable moment," are delivered a brief, motivational intervention matched to their level of risk.
Primary Outcome Measure Information:
Title
Alcohol Use Disorders Identification Test (AUDIT) Total
Description
The primary outcome measure will come from the participant's total score on the AUDIT. Scores on the AUDIT range from 0 to 40 with higher numbers indicating greater problematic alcohol use. Mean AUDIT scores at follow-up will be compared between arms.
Time Frame
Baseline, Follow-up (Up to 7 months)
Secondary Outcome Measure Information:
Title
AUDIT-C or Drinkers Index
Description
The drinkers index consists of a summary of the first three AUDIT items which represents a combination of quantity, usual frequency, and frequency of heavy drinking. The AUDIT-C can range from 0 to 12 with 12 representing higher levels of drinking quantity and frequency.
Time Frame
Baseline, Follow-up (Up to 7 months)
Title
Controlled Drinking Self-Efficacy Scale (CDSES)
Description
The 20-item Controlled Drinking Self-Efficacy Scale (CDSES), is a reliable, valid, easy-to-administer scale that assesses confidence to reduce overall consumption and frequency of drinking. Items range from 0% to 100% with 100% indicating more confidence to engage in controlled drinking. The CDSES was administered at both baseline and follow-up to assess changes in this presumed mediating attitude.
Time Frame
Baseline, Follow-up (Up to 7 months)
Title
Readiness to Change Scale
Description
A readiness to change alcohol use measure (ranging from 1 - not ready to change, to 4 - very ready) was assessed at baseline and follow-up for all participants. Because motivation and readiness to change are hallmark elements of the SBIRT approach and are thought to be integral to behavior change, these constructs will be measured to assess the degree to which they change in the two groups. Some individuals may not abstain or reduce their use over time, but there may be an improvement in their readiness to change.
Time Frame
Baseline, Follow-up (Up to 7 months)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: 18 or Older Active Duty Off Duty Telephone Number for Follow-up Healthy Enough to Participate Positive Screen for Risky Drinking Exclusion Criteria: Under 18 Non-Military On Duty Low Level Drinking
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mark Reed, PhD
Organizational Affiliation
SDSURF - Center for Alcohol & Drug Studies & Services
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Gerard DeMers, DO
Organizational Affiliation
United States Naval Medical Center, San Diego
Official's Role
Principal Investigator
Facility Information:
Facility Name
Naval Medical Center San Diego
City
San Diego
State/Province
California
ZIP/Postal Code
92134
Country
United States

12. IPD Sharing Statement

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Alcohol Screening, Brief Intervention, and Referral to Treatment in a Military Treatment Facility

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