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NOT YET RECRUITING
NCT07894289
EARLY_PHASE1

Examining the Role of Sensitivity to Uncertain Threat and Alcohol Response in Risk for Alcohol Use Disorder Following Sexual Assault in College Women

Sponsor: Ohio State University

View on ClinicalTrials.gov

Summary

The goal of this clinical trial is to determine whether women who engage in heavy drinking with a history of sexual assault (SA) victimization show heightened baseline reactivity to uncertain threat (U-threat), whether alcohol reduces this reactivity and related anxiety, and how these processes link to real-world drinking behavior. The main questions it aims to answer are: * Test whether heavy drinking women with a history of SA display exaggerated baseline reactivity to U-threat. * In the lab, test whether alcohol intoxication is associated with decreases in reactivity to U-threat and subjective anxiety, particularly in heavy drinking women with a history of SA. * In the real-world, test associations between SA victimization, reactivity to U-threat, alcohol consumption, and anxiolytic relief. Participants will: * Complete a screening and orientation session * Complete two experimental lab sessions that will include intravenous (IV) administration of either 80mg% alcohol or placebo (saline), order counterbalanced * Complete daily ecological momentary assessments (EMA) surveys for 21 days * Wear a transdermal alcohol wrist biosensor (BACTrack Skyn) for 21-days

Key Details

Gender

FEMALE

Age Range

21 Years - 29 Years

Study Type

INTERVENTIONAL

Enrollment

220

Start Date

2026-12

Completion Date

2031-08

Last Updated

2026-10-26

Healthy Volunteers

No

Interventions

DRUG

Alcohol

Participants will receive 80 mg% intravenous alcohol.

DRUG

Placebo

Participants receive placebo (saline) intravenously.

Locations (1)

Ohio State University

Columbus, Ohio, United States