Actively Recruiting

Phase Not Applicable
Age: 21Years - 30Years
All Genders
Healthy Volunteers
ID05701865

Biphasic Effects of Acute Alcohol Intoxication on Bystander Intervention for Sexual Violence

Led by Georgia State University · Updated on 2024-06-12

192

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating how alcohol intoxication, gender, and bystander attitudes affect barriers to intervening and sexual violence prevention among young adults aged 21 to 30. The study aims to understand if alcohol and gender influence bystander barriers and intervention behaviors, and whether alcohol's impact varies depending on gender and prosocial attitudes toward helping others. Participants will be randomly assigned to receive either an alcoholic beverage designed to reach a breath alcohol concentration of 0.08% or a non-alcoholic control beverage. Those receiving alcohol will complete study tasks either while their blood alcohol level is rising or falling. All participants will imagine themselves in a risky sexual violence scenario to assess their perceived barriers and intentions to intervene. During the study, researchers will measure participants' thoughts about barriers to intervening and their intentions to act as bystanders between 35 minutes and 2.5 hours after drinking. The study includes behavioral assessments and compares responses between the alcohol and control groups as well as between men and women. Participation involves monitoring and evaluation over a short time frame during the experimental session.

CONDITIONS

Brief Title

Biphasic Effects of Acute Alcohol Intoxication on Bystander Intervention

Who Can Participate

Age: 21Years - 30Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Between the ages of 21 and 30
  • Report drinking alcohol on at least 3 days in the past year at levels equal to or greater than the study dose
Not Eligible

You will not qualify if you...

  • Currently seeking treatment or recovering from alcohol or substance use disorder
  • Have a medical condition or take medication that makes alcohol consumption unsafe
  • Pregnant, nursing, or have had sexual intercourse without effective contraception in the past two weeks
  • Weigh over 250 pounds if under six feet tall, or over 300 pounds if over six feet tall

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

Duration - Single session lasting up to 2.5 hours

Participants receive either a moderate alcohol dose or a no alcohol control beverage and complete study tasks related to bystander intervention.

1 visit (in-person)

Trial Site Locations

Total: 1 location

1

Georgia State University

Atlanta, Georgia, United States, 30302

Actively Recruiting

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Research Team

R

Ruschelle M Leone, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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