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Completed

NCT Number: NCT06776796

Testing the Efficacy of a Brief Alcohol Intervention Among College Students

Individuals will be recruited to participate in a randomized controlled trial to test the efficacy of a prevention program aimed at reducing alcohol use among college students. If randomized to the intervention, participants will view personalized content based on their alcohol use and chosen identity and learn about various topics related to alcohol use, including ways to reduce their use. Control participants will be directed to a website where information regarding mental health and substance use may be found. Baseline mental health, alcohol use, and related constructs will be assessed. Participants will complete a 3-month follow-up survey to assess the efficacy of the tool in symptom reduction.

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Key information

Age range

18 year–25 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Georiga State University

Atlanta, Georgia, 30303, United States

About this study

Students will be recruited by campus flyers, social media, and a registrar list to participate in a randomized controlled trial (RCT) to test the efficacy of a prevention program aimed at reducing alcohol use among college students. Participants will also be recruited from a list of students who completed the Panthers4Life community needs assessment. Interested students will first complete a screener to determine eligibility (i.e., enrolled GSU student, 18-25 years of age, identifies as Black, White and LGBTQA+, Latine/a/o or Hispanic, and engaged in heavy episodic drinking at least once in the past month). Individuals who identify their sex at birth to be intersex or who identify themselves to be both heterosexual and gender diverse (Transgender, Genderqueer, Gender non-conforming, Non-binary, Androgynous, and Two-spirit) will be excluded due to the lack of normative data about these groups. Eligible participants will immediately be given the informed consent and asked to complete a baseline survey (15 minutes). In the baseline survey, participants will select identity group(s) they most identify with and select identity group(s) they would like to receive personalized normative feedback about. Participants will then be randomized to either complete a brief online intervention (treatment group) or view website information about substance use and mental health (control group).

If randomized to the intervention, participants will complete an intervention in Qualtrics Survey Platform that takes approximately 15 minutes to complete. They will view personalized content based on their alcohol use and chosen identity (e.g., if a participant chooses woman and LGBQA+ they will receive personalized normative feedback for women LGBQA+ students at GSU) and learn about various topics related to alcohol use, including ways to reduce their use. The intervention is a modified version of an existing evidence-based program, the Brief Alcohol Screening and Intervention for College Students (BASICS).

Participants assigned the control condition will be directed to a website where information regarding mental health and substance use may be found.

In both groups, the investigators will assess baseline mental health, alcohol use, and related constructs. Both groups will also be asked to complete a 3-month follow-up survey to assess the efficacy of the tool in symptom reduction. Cultural acceptability will also be assessed to determine if cultural adaptations are needed to enhance efficacy among groups represented in our sample. Participants will be compensated up to $30 in Amazon gift cards for their time ($15 for the baseline survey and $15 for the 3-month follow up).

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • 18-25 years old
  • Current student at university of study
  • Valid email address at university of study
  • Identifies as Black, White and LGBTQA+, Latine/a/o or Hispanic,
  • Endorse engaging in heavy episodic drinking at least once in the past month on the screening survey

Exclusion criteria

  • Individuals who identify their sex at birth as intersex or who identify as both heterosexual and gender diverse (Transgender, Genderqueer, Gender non-conforming, Non-binary, Androgynous, and Two-spirit) will be excluded due to the lack of normative data about these groups.

Treatment and study plan

Online Personalized Normative Feedback Intervention Targeting Alcohol Misuse

Behavioral

This is an integrated social norms-based personalized feedback intervention for college students targeting alcohol misuse. It is tailored by the identities chosen by participants including gender, race/ethnicity, and sexual orientation. The intervention is a modified version of an existing evidence-based program, the Brief Alcohol Screening and Intervention for College Students (BASICS) (Dimeff, et. al, 1999).

Mental Health and Substance Use Resources

Behavioral

Participants were directed to a website where information regarding mental health and substance use may be found.

Primary outcomes

  1. Changes in Alcohol use

    Time frame: Baseline and 3-months

    Number of drinks will be assessed using the daily drinking questionnaire. Higher scores indicate higher alcohol use.

Sponsors and collaborators

Lead sponsor

Georgia State University

Other

Registry information

Official study title

A Pilot Randomized Controlled Trial to Test the Efficacy of a Brief Alcohol Intervention Among College Students

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
Jan 15, 2025
Registry last updated
Jan 15, 2025

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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