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Integrated Alcohol and Sexual Assault Prevention for Bisexual Women

Integrated Alcohol and Sexual Assault Prevention for Bisexual Women

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05646446
Enrollment
0
Registered
2022-12-12
Start date
2023-08-03
Completion date
2025-03-21
Last updated
2025-03-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alcohol Use, Unspecified, Sexual Assault

Brief summary

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.

Interventions

BEHAVIORALREACH Program

The REACH program addresses alcohol use, sexual assault risk, and experiences relating to harm among bisexual women.

Sponsors

Lifespan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 24 Years
Healthy volunteers
Yes

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-binary * identify 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 Inventory * current symptoms of alcohol use withdrawal on the Alcohol Use Withdrawal Checklist

Design outcomes

Primary

MeasureTime frameDescription
Alcohol UseChange from baseline alcohol use at 4 months.The number of past month drinking days (Minimum = 0, Maximum = 31), average drinks per drinking day (Minimum = 0, Maximum = unspecified), number of heavy drinking days (Minimum = 0, Maximum = 30), assessed via the Time Line Follow Back, with greater scores meaning worse outcomes)
Sexual VictimizationReductions in comparison to control at 4 months.Assessed via the Sexual Experiences Survey. Summary score calculated that reflects both frequency and severity (Minimum = 0, Maximum = 63). Higher scores mean worse outcomes.

Secondary

MeasureTime frameDescription
AnxietyChange from baseline at 4-months.Assessed via the Generalized Anxiety Disorder 7 (GAD-7) (Minimum = 0, Maximum = 21), with higher scores meaning worse outcomes.
DepressionChange from baseline at 4-months.Assessed via the Patient Health Questionnaire 9 (PHQ-9) (Minimum = 0, Maximum = 27), with higher scores meaning worse outcomes.
MindfulnessChange from baseline at 4-months.Assessed via the Mindful Attention and Awareness Scale (Minimum = 15, Maximum = 90), with higher scores meaning better outcomes.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026