- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05729256
Alcohol and "Heat of the Moment" Sexual Decision Making
Alcohol and "Heat of the Moment" Sexual Decision Making Among MSM: Identifying Mechanisms of Sexual Risk and Promoting Behavior Change Through Brief Intervention
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Despite prevention efforts over the past two decades, HIV transmission remains a significant public health concern, especially among men who have sex with men (MSM). Approximately 65% of new HIV diagnoses in the United States are due to male-to-male sexual contact. Condomless anal intercourse (CAI) continues to be the major route of transmission for MSM. Thus, to reduce the incidence of HIV, it is critical to identify risk factors that underlie HIV acquisition and transmission and develop behavioral strategies that modify them directly or reduce the influence of these factors on behavior. Alcohol use, particularly heavy episodic drinking, is a central modifiable risk factor that may increase CAI in conjunction with other contextual variables. Although there have been a limited number of HIV prevention interventions that incorporate alcohol in sexual risk reduction efforts, relatively little is known about how such interventions impact sexual decision-making in "heat-of the-moment", particularly while intoxicated and in high arousal states that commonly are proximal to sexual behavior.
The goals of this study are to: (1) better understand the within-person mechanisms linking alcohol and arousal with CAI and (2) test the efficacy of an HIV prevention intervention approach that both reduces alcohol consumption and mitigate the influence of intoxication and arousal on CAI. These complementary objectives are addressed through an experience sampling method study (ESM) that examines the impact of an HIV prevention intervention that targets sexual risk and alcohol use. This study will examine whether mechanisms that underlie sexual risk in the natural environment and can be modified by intervention.
In the proposed study, non-monogamous adult MSM who engage in heavy drinking and CAI will be randomly assigned to an intervention condition that addresses alcohol use and sexual decision-making in "heat-of-the-moment" situations. The intervention will be preceded and followed by 3-week ESM bursts of intensive longitudinal assessment of alcohol use, arousal, sexual delay discounting, working memory, and CAI. 4-month follow-up data will be collected. Results will contribute to the long-term goal of enhancing effectiveness of behavioral HIV prevention interventions that address alcohol use.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Tibor Palfai, PhD
- Phone Number: 6173539345
- Email: palfai@bu.edu
Study Contact Backup
- Name: Maya Kratzer
- Email: mkratzer@bu.edu
Study Locations
-
-
Massachusetts
-
Boston, Massachusetts, United States, 02215
- Recruiting
- Boston University Department of Psychological and Brain Sciences
-
Contact:
- Tibor P. Palfai, PhD
- Phone Number: 617-353-9345
- Email: palfai@bu.edu
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- At least 18 years of age
- Cisgender man who has had condomless anal intercourse with another man in the past 3 months
- Engaged in heavy drinking (assessed by either weekly National Institute on Alcohol Abuse and Alcoholism guidelines [> 14 for men], and/or a heavy drinking episode in the past month [> 4 drinks on an occasion])
- Has a smartphone
Exclusion Criteria:
- HIV-infection
- Currently using PrEP
- In an exclusive monogamous sexual relationship
- History of bipolar disorder, schizophrenia, other psychotic disorder, or current suicidal intent
- Current treatment for alcohol use disorder or substance use disorder
- Unable to provide one or more individuals who can serve as an alternate contact
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Self-Regulation Intervention
Single session motivational intervention on reducing heavy drinking and sexual risk behavior, encouraging consideration of pre-exposure prophylaxis (PrEP), followed by 4 weeks of text messages on content relevant to drinking goals and support for healthy sexual choices
|
Single session motivational intervention on reducing heavy drinking and sexual risk behavior, encouraging consideration of pre-exposure prophylaxis (PrEP), followed by 4 weeks of text messages on content relevant to drinking goals and support for healthy sexual choices
|
|
Active Comparator: Brief Advice and Information
Single session to provide psychoeducation about heavy drinking risks, discussion of barriers to safe sex, information about pre-exposure prophylaxis (PrEP)
|
Psychoeducation about heavy drinking risks, discussion of barriers to safe sex, information about pre-exposure prophylaxis (PrEP)
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Count of number of times engaged in Condomless Anal Intercourse (CAI) from Sexual Behavior Survey
Time Frame: Past 90 days
|
Self-reported number of times engaged in CAI
|
Past 90 days
|
|
Heavy Drinking Episodes from the Quick Drinking Screen
Time Frame: Past 90 days
|
Self-reported number of days consumed 5 or more standard drinks
|
Past 90 days
|
|
Average number of drinks per week from the Quick Drinking Screen
Time Frame: Past 90 days
|
Self-reported average number of drinks per week multiplied by frequency of drinking per week
|
Past 90 days
|
|
Condomless Anal Intercourse: Experience Sampling
Time Frame: ESM assessments over a 3 week period
|
Self-reported frequency of CAI from experience sampling questions
|
ESM assessments over a 3 week period
|
|
Alcohol Use: Experience Sampling
Time Frame: ESM assessments over 3 week period
|
Self-reported number of drinks and perceived intoxication (composite variable)
|
ESM assessments over 3 week period
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Tibor Palfai, PhD, Boston University
Publications and helpful links
General Publications
- Sobell LC, Agrawal S, Sobell MB, Leo GI, Young LJ, Cunningham JA, Simco ER. Comparison of a quick drinking screen with the timeline followback for individuals with alcohol problems. J Stud Alcohol. 2003 Nov;64(6):858-61. doi: 10.15288/jsa.2003.64.858.
- Gordon CM, Carey MP, Carey KB. Effects of a drinking event on behavioral skills and condom attitudes in men: implications for HIV risk from a controlled experiment. Health Psychol. 1997 Sep;16(5):490-5. doi: 10.1037//0278-6133.16.5.490.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 6603e
- R01AA030461-01 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Data will be shared following release within one year of the trial end to investigators who make specific requests in writing regarding analysis plans. Plans will be reviewed with co-investigators to ensure that there is no overlap with planned analyses. Specific de-identified data set will be provided to other researchers after this review.
In addition, data will be shared according to the guidelines for the National Institute of Mental Health Data Archive (NDA)
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- ICF
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Alcohol Drinking
-
University of North Carolina, Chapel HillNational Institute on Alcohol Abuse and Alcoholism (NIAAA)CompletedDrinking Behavior | Adolescent Behavior | Drinking, Alcohol | Alcohol Drinking, AdolescentUnited States
-
University of Auckland, New ZealandTe Hiringa Hauora/Health Promotion AgencyCompletedDrinking, Alcohol | Consumption, AlcoholNew Zealand
-
Penn State UniversityNot yet recruiting
-
Boston University Charles River CampusActive, not recruiting
-
The Hong Kong Polytechnic UniversityNot yet recruitingHazardous Drinking | Harmful Alcohol Use
-
University of WyomingRecruiting
-
Binghamton UniversityNot yet recruitingUnderage Drinking | Drinking, Teen | Adolescent Alcohol UseUnited States
-
Butler HospitalNational Institute of General Medical Sciences (NIGMS)CompletedDrinking, AlcoholUnited States
-
The University of Hong KongRecruitingmHealth Intervention | AlcoholHong Kong
-
Real Prevention, LLCCompletedUnderage Drinking | Alcohol Use, UnderageUnited States
Clinical Trials on Self-Regulation Intervention
-
University of MichiganEunice Kennedy Shriver National Institute of Child Health and Human Development...CompletedMedication Adherence | Self-regulationUnited States
-
University of California, DavisActive, not recruitingInfant Behavior | Infant Development | Self-Control | Self-Regulation, EmotionUnited States
-
University of North Carolina, Chapel HillCompletedObesity | Weight Loss | Weight Gain PreventionUnited States
-
University of MichiganNational Institute on Aging (NIA)Completed
-
Boston CollegeJoslin Diabetes CenterCompleted
-
UNC Lineberger Comprehensive Cancer CenterCompletedBreast Neoplasms | Body Weight ChangesUnited States
-
University of HoustonAmerican Cancer Society, Inc.; Herald Cancer AssociationCompletedBreast Cancer | Breast NeoplasmsUnited States
-
Wayne State UniversityCompletedHypertension | HemodialysisUnited States
-
Columbia UniversityNational Institute on Aging (NIA)Completed
-
Saglik Bilimleri UniversitesiActive, not recruiting