Evaluating Cross-Cutting Prevention at the U.S. Air Force Academy

NCT06875284 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 2041

Last updated 2025-11-25

Study results available
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Summary

Sexual assault and alcohol misuse are interrelated, persist at high rates in military populations, and carry negative consequences for military units and personnel. Combining tailored efforts to prevent sexual assault and alcohol misuse is critical for developing a more effective Force. This study will test the cross-cutting immediate and long-term outcomes of two programs, the Sexual Communication and Consent (SCC) sexual assault prevention program and the eCHECKUP TO GO alcohol misuse prevention program, delivered separately and in combination, with Cadets at the United States Air Force Academy. Anonymous Cadet self-report data will be collected before training (pre-test), immediately after training (post-test), 3 months after training (Fall semester follow-up), and 9 months after training (Spring semester follow-up).

Conditions

  • Sexual Assault
  • Alcohol Misuse

Interventions

BEHAVIORAL

Sexual Communication and Consent (SCC)

SCC combines universal classroom instruction with tailored web-based content. Based on sociodemographic characteristics and prior sexual assault experiences, Cadets receive tailored content that addresses either primary victimization prevention, revictimization prevention, or healthy relationships and bystander intervention promotion.

BEHAVIORAL

Alcohol eCHECKUP TO GO (eCHECKUP TO GO)

eCHECKUP TO GO is a personalized, online intervention designed to reduce cognitive risk factors for alcohol misuse. eCHECKUP TO GO is brief, self-guided, and provides individualized feedback based on a user's self-reported alcohol use patterns and consequences.

BEHAVIORAL

Training as usual (TAU)

TAU involves universal classroom instruction focused on developing knowledge, attitudes, and skills to promote personal resilience, increase potential for success, and develop healthy and rewarding personal relationships.

Sponsors & Collaborators

  • U.S. Army Medical Research Acquisition Activity

    collaborator FED
  • U.S. Army Medical Research and Development Command

    collaborator FED
  • University of Florida

    collaborator OTHER
  • San Diego State University

    collaborator OTHER
  • United States Department of Defense

    collaborator FED
  • RTI International

    lead OTHER

Principal Investigators

  • Marni L Kan, PhD · RTI International

  • Nichole M Scaglione, PhD · University of Florida

  • Emily A Schmied, PhD · San Diego State University

Study Design

Allocation
NON_RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
17 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-06-27
Primary Completion
2024-05-01
Completion
2024-05-01

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06875284 on ClinicalTrials.gov