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NCT Number: NCT05011903

Integrative Alcohol and Risky Sex Feedback for College Students

Alcohol misuse and related risky sexual behaviors are significant health concerns for college students. Two-thirds of students are current drinkers, at least 1 in 3 report past month heavy episodic drinking (5+ drinks in a row), and 1 in 10 report high intensity drinking (10+ drinks in a row). Increased student alcohol use and heavy drinking are linked to increased sexual activity and related risky behaviors (e.g., unprotected sex, sex with casual partners). This puts students at risk for negative health outcomes (e.g., STIs - sexually transmitted infections) and is also a pathway to sexual victimization and escalated drinking. The first few weeks of college, known as the 'red zone,' provide an opportunity to intervene at time when these behaviors increase. However, most prevention programs for college students tend to focus on student alcohol use and have little to no integration of content on the relationship between alcohol use and risky sexual behaviors. This is an important gap in the literature and a priority area for NIAAA. The research team established the short-term efficacy of a personalized feedback intervention (PFI), a gold standard intervention approach, with integrated content on alcohol and risky sexual behaviors. In this study, we propose to extend our integrated PFI to include a cross-tailored dynamic feedback (CDF) component. The CDF component will use technology to incorporate daily assessments of student behavior and provide students with dynamic weekly feedback over 12 weeks. The goal is to increase the effectiveness of the integrated PFI and to create a program that is easily implemented on college campuses.

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Key information

Age range

18 year–20 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Kentucky, Lexington, Kentucky, United States

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About this study

The project utilizes a multisite, hybrid type 1 effectiveness-implementation study design to (1) evaluate the impact of CDF for first-year college students and (2) identify implementation factors critical to its success to facilitate future scale-up in campus settings. The first aim is to conduct a multi-level stakeholder-engaged adaptation of the integrated alcohol and risky sex PFI through the development and inclusion of CDF. The second aim is to conduct a randomized controlled trial (RCT) of the enhanced intervention (PFI+CDF) in a sample of 600 first-year college students. The primary hypothesis is that participants who receive the PFI+CDF intervention will report less alcohol use, fewer risky sexual behaviors, and fewer consequences relative to those who receive a PFI supplemented with generic health information at follow-up (1, 2, 3, 6, and 13 months). Participants (N=600 total, 300 per site) will be randomized to 1 of 4 groups: (1) PFI+CDF with weekend diary surveys, (2) PFI+GHI with weekend diary surveys, (3) PFI-only, no weekend diary surveys, and (4) assessment-only control, no weekend diary surveys. All participants will complete a baseline survey during the first week of the semester, be randomly assigned to condition, and complete follow-up surveys at 1, 2, 3, 6, and 13 months. This staggered design allows for comparison of the enhanced PFI+CDF relative to the PFI+GHI condition, which may be consistent with a "treatment-as-usual" comparison group (e.g., of the universities that have adopted an evidence-guided alcohol intervention program for their campus, many currently deliver commercialized alcohol-focused PFIs to incoming first-year students). Providing weekly GHI in the comparison condition allows for an equal number of "exposures" between the more intensive conditions (PFI+CDF vs. PFI+GHI), analogous to an attention control group, offering a clearer understanding of the overall impact of the PFI+CDF adaptation. The inclusion of two PFI conditions, one with weekend diary assessments and one without allows us to control for potential assessment reactivity that might result from the diary-style assessment approach. Overall, this design is intended to allow a separation of the "true" intervention effect of the CDF above and beyond the effect of assessment reactivity. The PFI-only vs. assessment-only control group comparison will provide a test of basic efficacy of the integrated PFI that has been adapted based on stakeholder feedback. The third aim seeks to identify factors critical to PFI+CDF implementation in campus settings through conducting focus groups with a subset of students from the RCT and with local and national systems-level stakeholders. The intervention has strong potential for widespread dissemination and targets a group at high risk for alcohol misuse and RSB.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • status as first-year college student at University of Kentucky or UNT-Denton
  • 18-20 years old

Exclusion criteria

  • the inability or unwillingness to give informed, voluntary consent to participate
  • not meeting inclusion criteria
  • currently in treatment to reduce alcohol or other substance use
  • pregnant or planning to become pregnant

Treatment and study plan

Cross-tailored Dynamic Feedback

Behavioral

Dynamic, technology-delivered weekly feedback on weekend diary self-reports of first-year college student behavior related to alcohol use and related sexual behaviors.

Personalized Feedback Intervention

Behavioral

Technology-delivered personalized feedback on first-year college student behavior related to alcohol use and related sexual behaviors.

Dynamic Feedback on General Health Behaviors

Behavioral

Dynamic, technology-delivered weekly feedback on weekend diary self-reports of first-year college student behavior related to general health behaviors.

Primary outcomes

  1. Change in self-reported alcohol-related sexual behavior frequency

    Time frame: Baseline, 1-month, 2-month, 3-months, 6-months, and 13-months

    Number of times alcohol was consumed during or before sex in the last month

  2. Change in self-reported alcohol-related sexual behavior quantity

    Time frame: Baseline, 1-month, 2-month, 3-months, 6-months, and 13-months

    Number of alcoholic beverages consumed before sex in the last month

  3. Change in self-reported alcohol-related hook-ups

    Time frame: Baseline, 1-month, 2-month, 3-months, 6-months, and 13-months

    Number of alcohol-related hook-ups experienced in the last month

  4. Change in self-reported alcohol-related sexual behavior consequences

    Time frame: Baseline, 1-month, 2-month, 3-months, 6-months, and 13-months

    Number of alcohol-related sexual consequences experienced in the last month

Secondary outcomes

  1. Change in self-reported alcohol use quantity

    Time frame: Baseline, 1-month, 2-month, 3-months, 6-months, and 13-months

    Typical number of drinks consumed on each day of week in the last month

  2. Change in self-reported heavy episodic drinking

    Time frame: Baseline, 1-month, 2-month, 3-months, 6-months, and 13-months

    Number of heavy drinking episodes (4+ drinks female, 5+ drinks male) in the last month

  3. Change in self-reported quantity of sex partners

    Time frame: Baseline, 1-month, 2-month, 3-months, 6-months, and 13-months

    Number of casual sex partners in the last month

  4. Change in self-reported condom use

    Time frame: Baseline, 1-month, 2-month, 3-months, 6-months, and 13-months

    Number of times condom was used during sex in the last month

Study contacts

Contact information is provided by the study sponsor or research team.

Anne E Ray, PhD

CONTACT

[email protected]

8592184944

Sponsors and collaborators

Lead sponsor

Anne E Ray

Other

Collaborators

  • Klein Buendel, Inc.
  • National Institute on Alcohol Abuse and Alcoholism (NIAAA)
  • University of North Texas Health Science Center

Registry information

Official study title

Cross-Tailoring Integrative Alcohol and Risky Sex Feedback for College Students: A Hybrid Type 1 Effectiveness-Implementation Trial

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Aug 18, 2021
Registry last updated
Jun 12, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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