Project Guard: Reducing Alcohol Misuse/Abuse in the National Guard
NCT ID: NCT02860442
Last Updated: 2021-09-29
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
850 participants
INTERVENTIONAL
2017-03-01
2021-05-31
Brief Summary
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Detailed Description
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The specific aims of the study are to compare SP-BI and EUC in: 1) Reducing the frequency and intensity of at-risk drinking at 4 -, 8- and 12-months; 2) Decreasing binge drinking at 4-, 8- and 12 months. The secondary aims are to: 1) Compare the SP-BI and EUC conditions in reducing the frequency of illicit drug use and depressive symptoms at 4-, 8- and 12-months; 2) Examine if deployment status moderates the effect of intervention assignment (SP-BI or EUC) on post-intervention drinking, depressed feelings, and other substance use.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
NONE
Study Groups
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Smartphone brief intervention (SP-BI)
Smartphone brief intervention (SP-BI)
Participants in the SP-BI group will receive a 20-30 minute intervention through an app program based on the FRAMES format: providing personalized Feedback (regarding substance use, risk factors), emphasis on Responsibility for change, Advice, Menu of options, Empathic clinical behaviors, and support of Self-efficacy regarding making changes. The intervention is designed to address the target behavior of alcohol use, and will include a tailored review of participants' goals/values, feedback regarding their alcohol use patterns and consequences (either actual experiences or potential based on risk behaviors), developing a discrepancy between their alcohol use and ability to meet goals and values through a decisional balance exercise, and formulation of a "change plan".
Enhanced Usual Care (EUC)
Enhanced Usual Care (EUC)
Those assigned to EUC will receive an informational brochure with resources available to members of the military related to mental health and alcohol use. They will be contacted to complete 4-, 8-, and 12-month follow-up assessments.
Interventions
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Smartphone brief intervention (SP-BI)
Participants in the SP-BI group will receive a 20-30 minute intervention through an app program based on the FRAMES format: providing personalized Feedback (regarding substance use, risk factors), emphasis on Responsibility for change, Advice, Menu of options, Empathic clinical behaviors, and support of Self-efficacy regarding making changes. The intervention is designed to address the target behavior of alcohol use, and will include a tailored review of participants' goals/values, feedback regarding their alcohol use patterns and consequences (either actual experiences or potential based on risk behaviors), developing a discrepancy between their alcohol use and ability to meet goals and values through a decisional balance exercise, and formulation of a "change plan".
Enhanced Usual Care (EUC)
Those assigned to EUC will receive an informational brochure with resources available to members of the military related to mental health and alcohol use. They will be contacted to complete 4-, 8-, and 12-month follow-up assessments.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Those who do not have access to a smart phone with either Android or iOS operating system
* Those in active treatment for substance use disorders (i.e., report addictions treatment in past 4 months) will be excluded because the proposed SBIRT intervention is focused on early brief intervention for those with at-risk drinking and on referral to treatment for those with more serious problems
ALL
No
Sponsors
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Case Western Reserve University
OTHER
University of Michigan
OTHER
University of Toledo Health Science Campus
OTHER
Keming Gao
OTHER
Responsible Party
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Keming Gao
Director, Mood Disorders Program
Principal Investigators
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Frederic C Blow, PhD
Role: PRINCIPAL_INVESTIGATOR
Department of Psychiatry, University of Michigan
Locations
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University Hospitals Cleveland Medical Center
Cleveland, Ohio, United States
University of Toledo
Toledo, Ohio, United States
Countries
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Provided Documents
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Document Type: Study Protocol and Statistical Analysis Plan
Other Identifiers
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CDMRP-13277015
Identifier Type: OTHER_GRANT
Identifier Source: secondary_id
03-16-11
Identifier Type: -
Identifier Source: org_study_id
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