Peer Influences in Alcohol and Sexual Violence Among Marines Dyads

March 18, 2026 updated by: Amanda Gilmore, Georgia State University

Examining Peer Influences in Alcohol and Sexual Violence Among Marines Using a Dyadic Multimethod Approach

The goal of this experimental study is to examine the complex and multifaceted influence of peers on alcohol-involved sexual violence perpetration (ASVP) in U.S. Marine Corps (USMC) men. The specific aims are:

Aim 1: Use ecological momentary assessment (EMA) to examine event-level effects of one's own alcohol use, peer alcohol use, and injunctive norms on ASVP intentions among dyads of Marine men who drink together (n=160 dyads; 320 total participants).

Aim 2: Examine the individual and peer effects on ASVP behavior in an experimental paradigm with a gender x confederate (potential victim) intoxication status design. In-the-moment dyad-peer verbalized encouragement for ASVP ("go cues") will be assessed by qualitatively coding verbalizations during the interaction.

Aim 3: Examine modifiable risk factors on ASVP intentions in vivo (Aim 1; EMA) and ASVP behavior in vitro (Aim 2; experiment) settings.

Participants will complete: 1) an individual orientation session with informed consent, baseline assessment, and EMA demo; 2) 14 days of EMA completed individually; and 3) a dyadic session to complete an experimental paradigm via videoconferencing. All study procedures will be completed in off-duty time as to not interfere with military duties.

Study Overview

Detailed Description

The overarching goal of this R01 is to obtain an event-level understanding of the role of alcohol and peer interpersonal behavior in sexual violence perpetration among Marine men. Rates of heavy episodic drinking and military sexual assault are high in the military, and highest among Marines. Alcohol is involved in 21-80% of sexual violence incidents among servicewomen and 14-56% of incidents among servicemen. Perceived peer norms and interpersonal interactions are key predictors of alcohol use and alcohol-involved sexual violence perpetration (ASVP) among civilians; however, it is unclear if these risk factors operate similarly in military populations. Peers in the US Marine Corps are unique and exert powerful influence on adaptive behaviors and attitudes and more negative health behaviors such as alcohol misuse. The proposed multi-method project, implemented by an experienced team of investigators, will simultaneously address several major and persistent gaps in knowledge. First, the investigators will obtain an event-level understanding of the effects of one's own and peer alcohol use, and the role of alcohol in ASVP norms on ASVP intentions in the US Marine Corps by integrating findings from in vivo and in vitro assessment methods. Second, this study will examine and assess the individual and peer effects of in-the-moment encouragement and discouragement on ASVP behaviors in an experimental paradigm. The investigators will accomplish this by leveraging innovative dyadic approaches employed among civilian dyads, thereby elucidating peer influences on ASVP among men in the US Marine Corps. The proposed study will recruit pairs of enlisted men currently serving in the US Marine Corps who engaged in heavy episodic drinking at least twice together in the past month. Dyads will complete ecological momentary assessments about their own and perceived peer alcohol use and ASVP intentions twice daily for 14 days. The study will also compare modifiable risk effects of peer influence acceptance of ASVP intentions and behaviors in vivo and in vitro settings.

Study Type

Observational

Enrollment (Estimated)

320

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Georgia
      • Atlanta, Georgia, United States, 30303
        • Recruiting
        • Georgia State University
        • Contact:
        • Principal Investigator:
          • Amanda K Gilmore, PhD

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Men aged 21 or older who drink alcohol and are currently serving in the United States Marine Corps (USMC).

Description

Inclusion Criteria:

  • Men
  • Aged 21 or older
  • Currently serving in the United States Marine Corps (USMC)
  • Marine dyads must have engaged in heavy episodic drinking (≥5 drinks in less than two hours) together at least twice in the past month
  • Marine dyads must rate their peer at a minimum of "somewhat important" on the Important People Interview.

Exclusion Criteria:

  • The only exclusion criteria is not meeting inclusion criteria.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Confederate Group: Intoxicated Man
Participants in this group are randomly assigned to complete the experiment with a confederate who is an intoxicated man.
Confederate Group: Sober Man
Participants in this group are randomly assigned to complete the experiment with a confederate who is a sober man.
Confederate Group: Intoxicated Woman
Participants in this group are randomly assigned to complete the experiment with a confederate who is an intoxicated woman.
Confederate Group: Sober Woman
Participants in this group are randomly assigned to complete the experiment with a confederate who is a sober woman.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Sexual Strategies Survey
Time Frame: For 14 days after enrollment
Alcohol-involved sexual violence intentions will be assessed using a modified version of the Sexual Strategies Survey. Scores range from 0-168, higher scores indicate higher intentions.
For 14 days after enrollment
Sexual Experiences Survey-Long Form Perpetration - Noncontact Items
Time Frame: For 14 days after enrollment
Alcohol-involved sexual violence intentions will be assessed using the noncontact items from the Sexual Experiences Survey-Long Form Perpetration (SES-LFP). Scores range from 0-49, higher scores indicate higher intentions.
For 14 days after enrollment
Sexual Imposition Task
Time Frame: Experiment at 14 days after enrollment
Alcohol-involved sexual violence perpetration behavior will be assessed using the Sexual Imposition Task. Choice of film and duration of clip will both be assessed.
Experiment at 14 days after enrollment

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Amanda K Gilmore, PhD, Georgia State University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 18, 2026

Primary Completion (Estimated)

July 1, 2030

Study Completion (Estimated)

August 31, 2030

Study Registration Dates

First Submitted

November 20, 2025

First Submitted That Met QC Criteria

November 20, 2025

First Posted (Actual)

December 1, 2025

Study Record Updates

Last Update Posted (Actual)

March 19, 2026

Last Update Submitted That Met QC Criteria

March 18, 2026

Last Verified

March 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

No sharing of individual participant data, only de-identified data.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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.

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