Alcohol & Men's Sexual Risk Behaviors
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Alcoholic Beverage, Non-alcoholic Beverage, Partner Negative Mood Manipulation, Partner Positive Mood Manipulation.
- Who it may be relevant to
- Registry conditions: Sexual Behavior, Alcohol Drinking, Sexual Aggression, Emotions. Basic parameters: 21 years — 30 years · Male.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Men's Sexual Risk Behaviors: Alcohol, Sexual Aggression, and Emotional Factors (Extension)
Overview
This project extends the investigators' previous research regarding the intersecting risks of alcohol, sexual risk behavior (SRB), and sexual aggression (SA) in male drinkers who have sex with women by examining the mediating and moderating roles of both intrapersonal and interpersonal emotional factors. While independent streams of research consistently document alcohol's role in SRB and SA, the investigators' work has demonstrated that these behaviors are related, and that alcohol exacerbates their likelihood both independently and synergistically. The researchers' investigations focus on a particular type of SRB: men's resistance to condom use with female partners who want to have protected sex. Condom use resistance (CUR) is common and normative among young male drinkers, with up to 80% of men reporting engaging in CUR. Of particular concern, research demonstrates that up to 42% of men report using coercive CUR tactics such as emotional manipulation, deception, condom sabotage, and force to obtain unprotected sex. Investigators will evaluate hypotheses that distal and proximal emotional and alcohol factors influence in-the-moment SRB/CUR intentions as well as daily alcohol use and SRB/CUR. The investigators will also examine whether the relationships among assessed variables are similar across experimental and naturalistic settings. That is, investigate the extent to which men's responses in the lab parallel their real-world drinking and SRB/CUR behaviors, particularly regarding self and partner emotions, empathy, and interpersonal stress.
Interventions
- Behavioral Alcoholic Beverage
Participants will consume an alcoholic beverage (vodka mixed with fruit juice) that is the equivalent of 3-4 standard alcoholic drinks based on their body weight. - Behavioral Non-alcoholic Beverage
Participants will consume a nonalcoholic beverage (fruit juice) that is the isovolemic equivalent of 3-4 standard alcoholic drinks based on their body weight. - Behavioral Partner Negative Mood Manipulation
Participants will engage in a laboratory task and will then report their own and their partner's emotions following the task. - Behavioral Partner Positive Mood Manipulation
Participants will engage in a laboratory task and will then report their own and their partner's emotions following the task.
Primary outcome measures
- Mean score of sexual risk intentions [Time frame: within one hour of receiving the intervention]
Secondary outcome measures (1)
- Sexual risk behavior [Time frame: 6 months]
Eligibility criteria
Inclusion criteria
- Single
- Male
- Ages 21-30
- Engagement in unprotected intercourse with a woman at least once in the past year
- Consumed alcohol at least 1 time per week in the past 30 days
- Had sex with a woman at least 2 times in the past 30 days
Exclusion criteria
- A history of alcohol problems
- A medical condition and/or medications which contraindicate alcohol consumption
- In a relationship that is monogamous and has lasted longer than 6 months
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Factorial
- Masking
- Single blind
- Primary purpose
- Basic science
Study locations
United States · 1 center
- Arizona State University — Phoenix
Identifiers
NCT: NCT06158880 · STUDY00018369 · 4R37AA025212