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Project Guard: Reducing Alcohol Misuse/Abuse in the National Guard

Not Applicable
Completed
Conditions
Alcohol Use
Interventions
Other: Enhanced Usual Care (EUC)
Behavioral: Smartphone brief intervention (SP-BI)
Registration Number
NCT02860442
Lead Sponsor
Keming Gao
Brief Summary

The overall goal for the study is to test the efficacy of a smartphone app which includes an alcohol brief intervention (SP-BI) versus an Enhanced Usual Care (EUC) condition for National Guard members in the State of Ohio who meet criteria for at-risk drinking in the previous 4 months. The main hypothesis is that those in the SP-BI group with have reduced frequency and intensity of at-risk drinking and fewer binge drinking episodes.

Detailed Description

The project is a fully-powered randomized controlled trial of a smartphone app which includes an alcohol brief intervention (SP-BI) versus an Enhanced Usual Care (EUC) condition for National Guard members in the State of Ohio, who are already participating in the Ohio Army National Guard Mental Health Initiative (OHARNG-MHI) study, titled "Resilience and Risk Factors Associated with Deployment Related Posttraumatic Psychopathology", who meet criteria for at-risk drinking in the previous 4 months. After tailoring the content of the SP-BI intervention for NG soldiers, the study will prescreen \~ 8,500 individuals over the three year enrollment period to identify 850participants with at-risk drinking. TParticipants in this study will be randomized to either the SP-BI (n=375) or the EUC condition (n=375) and followed at 4, 8 and 12 months post-enrollment. Participants who are randomized to the SP-BI condition will receive an informational brochure with resources available to members of the military related to mental health and alcohol use and will download a free app on to their smartphones. The app will be developed to be used on both Android and iPhone platforms and will be used over 12 weeks to deliver the study intervention. Those assigned to the EUC condition will receive the informational brochure only.

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.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
850
Inclusion Criteria
  • Have a past 4-month AUDIT-C score of 5 or more for men and 4 or more for women indicating that they meet criteria for at-risk drinking, AND
  • Do not meet any of the exclusion criteria.
  • Must be a current or former member of the Ohio Army National Guard (OHARNG) or U.S. Army Reserve based in Ohio.
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Enhanced Usual Care (EUC)Enhanced Usual Care (EUC)-
Smartphone brief intervention (SP-BI)Smartphone brief intervention (SP-BI)-
Primary Outcome Measures
NameTimeMethod
Change in the Number of Drinking Days as Assessed by the Audit-CChange over time (Baseline, 4-, 8- and 12-months post baseline)
Change in the Number of Drinks per Day as Assessed by the Audit-CChange over time (Baseline, 4-, 8- and 12-months post baseline)
Change in the Number of Binge Drinking Days as Assessed by the Audit-CChange over time (Baseline, 4-, 8- and 12-months post baseline)
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (2)

University Hospitals Cleveland Medical Center

🇺🇸

Cleveland, Ohio, United States

University of Toledo

🇺🇸

Toledo, Ohio, United States

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