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A SMART Evaluation of an Adaptive Web-based AUD Treatment for Service Members and Their Partners

Not Applicable
Recruiting
Conditions
Alcohol Abuse
Relations, Interpersonal
Military Family
Alcohol Drinking
Alcohol Use Disorder
Interventions
Behavioral: Gottman Self-Guided Resources
Behavioral: CRAFT Web-Based Intervention
Behavioral: Phone-Based CRAFT
Behavioral: CRAFT Workbook
Registration Number
NCT05619185
Lead Sponsor
Stanford University
Brief Summary

The purpose of this study is to evaluate the efficacy of an adaptive web intervention (Partners Connect) on military spouse drinking behaviors (CPs) and service member help-seeking (SMs). The investigators want to identify for whom this intervention is most efficacious and on what drinking behaviors and mechanisms. The investigators hypothesize that the intervention will reduce concerned partner drinking and increase service member help-seeking, compared to website resources, and that phone-based CRAFT will increase help-seeking behaviors, compared to those who are guided via a CRAFT workbook.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
744
Inclusion Criteria
  • at least 18 years of age;
  • be living together with their partner, with no plans to change that status in the next 2 months;
  • not be in the military themselves (to reduce concerns about mandated reporting of alcohol use);
  • score ≥4 on the AUDIT-C for females or ≥5 for males/other;
  • respond yes to "Do you feel safe in your current relationship?" from the Partner Violence Screen;
  • report not currently being in mental health or alcohol treatment (CP and SM)
  • understand English fluently,
  • be willing to try an online program to address risky drinking.

We require cohabitating CPs and SMs with no anticipated changes in the next two months to ensure close contact and opportunity to practice new skills, and those who would feel safe participating.

Exclusion Criteria
  • CPs in substance use treatment or their SM was in treatment in the last three months;
  • does not feel safe in the current relationship;
  • does not understand English fluently;
  • has an impaired capacity (cognitive, visual, or hearing);
  • is not cohabitating with their SM

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
InterventionPhone-Based CRAFTThose randomized to the CRAFT intervention will receive a web-based intervention
Phone Based CRAFTPhone-Based CRAFTIf a member of the recruited dyad does not respond, then participants will be randomized to receive phone-based CRAFT
ControlGottman Self-Guided ResourcesThose randomized to CONTROL will complete a self-guided intervention
Phone Based CRAFTCRAFT Web-Based InterventionIf a member of the recruited dyad does not respond, then participants will be randomized to receive phone-based CRAFT
InterventionCRAFT Web-Based InterventionThose randomized to the CRAFT intervention will receive a web-based intervention
CRAFT WorkbookCRAFT Web-Based InterventionIf a member of the recruited dyad does not respond, then participants will be randomized to receive a CRAFT workbook
InterventionCRAFT WorkbookThose randomized to the CRAFT intervention will receive a web-based intervention
CRAFT WorkbookCRAFT WorkbookIf a member of the recruited dyad does not respond, then participants will be randomized to receive a CRAFT workbook
Primary Outcome Measures
NameTimeMethod
Concerned Partner Drinking DaysBaseline to 6 month follow-up

The CP primary outcome is drinking defined as number of drinking days in the past month

Concerned Partner Drinks per EpisodeBaseline to 6 month follow-up

The CP primary outcome is drinking defined as number of drinks per episode in the past month

Service Member help-seekingBaseline to 6 month

Completion of the personalized normalized feedback (PNF) component of the intervention as a signal of increase help-seeking behavior

Secondary Outcome Measures
NameTimeMethod
mental health symptomsBaseline to 6 month follow-up

Depression as measured by the global score on the Patient Health Questionnaire 9-item (PHQ-9)

Trial Locations

Locations (1)

Stanford University

🇺🇸

Palo Alto, California, United States

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