Due to a study transfer between institutions, substantial time and funding was lost. Additionally, other federal funding cancellations resulted in a loss of staff.

This study will examine the effects of an incentive-based intervention (for reducing alcohol use) that would be sustainable, easily accessible intervention using remote alcohol monitoring and deposit contracts, targeting individuals who would not be reached by more traditional forms of treatment due to barriers such as time constraints, attitudes, and stigma.

Deposit contracts are effective at treating a wide variety of problems: smoking cessation, weight loss, and increasing physical activity. Despite the promise of deposit contracts, few earlier studies targeted problem drinking, since doing so required burdensome frequent monitoring - now overcome by remote alcohol monitoring. Earlier work relied on self- and collateral reports, breath alcohol concentrations during clinic visits, or an indirect non-specific marker of alcohol use. Despite these difficulties, earlier studies of deposit contracts were encouraging, with notable increases in: therapy participation; retention ; and abstinence duration compared to previous reports. Collectively, these studies show the potential of deposit contracts to reduce problem drinking but provide only limited evidence of its effectiveness. Still, these studies, and our recent success using contingency management with remote alcohol monitoring, provide a compelling rationale for examining whether a deposit contract program might provide a feasible, effective, and accessible way of helping people reduce drinking. Though there is limited systematic research on deposit contracts, deposit contract programs for various problems are widely available and have proven quite attractive. For example, a deposit contract weight loss website, has over 887,000 users with $62M in incentives paid. However, it is unclear if deposit contracts would be acceptable (and therefore feasible) to individuals interested in reducing their problem drinking. Therefore, we feel that the proposed deposit contract intervention utilizing remote alcohol monitoring could be a widely available and acceptable intervention for problem drinking for three reasons: (1) because of the effectiveness and convenience of our contingency management intervention using remote alcohol monitoring; (2) because of the widespread success of other deposit contract programs like DietBetã; and (3) because the potentially increased attractiveness and effectiveness of an intervention that can return an amount greater than the deposit. The adoption of a deposit contract intervention plus remote alcohol monitoring will only be accelerated by the "FitBit"-style alcohol monitoring devices being developed by many companies (we are currently independently evaluating one such device). However, making deposit contracts widely available will need evidence of their effectiveness, which requires large randomized controlled trials. The purpose of this R21 application is to develop this evidence by demonstrating that deposit contracts with remote alcohol monitoring are feasible and provide evidence of effectiveness needed to design and justify future studies.

Inclusion Criteria:

1. at least 21 years of age,
2. report at least 1heavy drinking episode during the last 28 days;
3. want to reduce their alcohol use;
4. are willing to wear a transdermal alcohol monitor;
5. own a smart phone and
6. are willing and able to deposit $30, $60, or $100 of their choice.

Exclusion Criteria:

1. substance use disorder (except alcohol, nicotine, and/or caffeine);
2. significant alcohol withdrawal symptoms (score ≥ 10 on the Clinical Institute Withdrawal Assessment for Alcohol) or currently in alcohol treatment;
3. medical condition that would contraindicate participation (e.g., pregnancy, scheduled surgery);
4. presence of a Diagnostic and Statistical Manual of Mental Disorders, 5th Edition (DSM-5) psychiatric disorder with symptoms of psychosis and/or delirium; or
5. inability to comprehend informed consent or instructions.

Since this is a research study, the investigators will share only de-identified where possible with:

• The sponsor of the study (the National Institutes of Health) and representatives of the sponsor assisting with the research
• The members of the local research team
• The Institutional Review Board and the Compliance Office of the University of Texas Health Science Center at San Antonio, and other groups that oversee how research studies are carried out.
• The Research offices at the University of Texas Health Science Center at San Antonio

The consent form will be shared on this site within 60 days of the last participant's last study visit to collect data.

The study protocol and statistical analysis plan will be shared on this site when results are reported after the study is completed.