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Alcohol Intoxication Effects on Bystander Intervention
N/A
Recruiting
Led By Ruschelle M Leone, PhD
Research Sponsored by Georgia State University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 35 minutes to 2.5 hours post-drinking
Awards & highlights
No Placebo-Only Group
Summary
This trial aims to explore how alcohol, gender, and bystander attitudes influence the likelihood of intervening in sexual violence scenarios.
Who is the study for?
This study is for men and women aged 21-30 who drink socially but aren't seeking treatment for alcohol or substance use disorders. They shouldn't have health conditions that make drinking unsafe, be pregnant or nursing, or at risk of pregnancy without effective contraception. Participants also need to meet specific height and weight criteria.
What is being tested?
Researchers are testing how being drunk affects young adults' willingness to intervene in risky sexual situations. The study looks at the effects of gender and attitudes towards helping others on this behavior by comparing a no-alcohol group with groups having different levels of drunkenness.
What are the potential side effects?
Since participants will consume alcohol, they may experience typical side effects like impaired judgment, coordination issues, mood changes, nausea, and hangover symptoms afterwards.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 35 minutes to 2.5 hours post-drinking
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~35 minutes to 2.5 hours post-drinking
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Articulated Thoughts of Barriers to Bystander Intervention
Articulated Thoughts of Intentions to Intervene as a Bystander
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Alcohol IntoxicationExperimental Treatment2 Interventions
Participant will receive alcohol, the dose of which will be administered to result in a breath alcohol concentration of .08%.
Group II: No-Alcohol ControlActive Control1 Intervention
Participant will receive a no alcohol control beverage, therefore their breath alcohol concentration will be .00%.
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Who is running the clinical trial?
Georgia State UniversityLead Sponsor
65 Previous Clinical Trials
30,514 Total Patients Enrolled
Ruschelle M Leone, PhDPrincipal InvestigatorGeorgia State University
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Eligibility Criteria:
This trial includes the following eligibility criteria:- I am between 21 and 30 years old.I am not pregnant, nursing, or have had unprotected sex recently.I am under 6 feet tall and weigh over 250 pounds, or I am over 6 feet tall and weigh more than 300 pounds.
Research Study Groups:
This trial has the following groups:- Group 1: Alcohol Intoxication
- Group 2: No-Alcohol Control
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.