Integrated Alcohol and Sexual Assault Prevention for Bisexual Women

The goal of this clinical trial is to develop and evaluate the preliminary efficacy of an intervention to address reducing alcohol use, sexual revictimization, and psychological distress among bisexual+ women (i.e., attraction to more than one gender: bisexual, pansexual, queer). The main questions the study seeks to answer are: 1) what is the feasibility of the recruitment method, research design, interventionist training methods, and delivery of the intervention; 2) does the intervention, relative to control, at the 2- and 4-month follow-up period, produce reductions in the quantity and frequency of alcohol use, sexual victimization, and psychological distress (anxiety, depression). Follow-up assessments are completed at 2- and 4-months following program completion. The intervention is compared to a wait list control group.

Inclusion Criteria:be between the ages of 18 and 24 years of age;identify as female gender or fluid, or gender non-conforming, gender queer, or non-binaryidentify as bisexual+ (i.e., attraction to more than one gender: bisexual, pansexual, queer);report a history of attempted or completed penetrative acts of sexual victimization (i.e., oral, vaginal, anal) since age 14 via coercion, incapacitation or force;report exceeding the national recommended limits for daily drinking (4 or more for women) on two or more occasions in the past month;report past month sexual activity.Exclusion Criteria:current suicide risk on the Beck Depression Inventorycurrent symptoms of alcohol use withdrawal on the Alcohol Use Withdrawal Checklist