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Phase 1 N=537 Randomized Single-blind Treatment

Alcohol Health Education Among College Drinkers

College Student Drinking

Enrolled (actual)
537
Serious AEs
0.0%
Results posted
Aug 2020
Primary outcome: Primary: Alcohol Consumption — 16.929; 17.988; 18.039 drinks

Study Design & Population

Study type
Interventional
Phase
Phase 1
Interventions
Alcohol 101 Plus (TM) (Behavioral); Booster (Behavioral); Lilly for Better Health (Behavioral)
Age
Adult · 18+ yrs
Sex
All
Sponsor
Abby Braitman
Primary completion
Sep 2014

Outcome Measures

OutcomeResultp-value
PRIMARY
Alcohol Consumption
16.929; 17.988; 18.039
SECONDARY
Alcohol-related Consequences
6.656; 7.156; 7.011

Summary

Alcohol use among college students is both widespread and problematic. There are many negative consequences associated with frequent alcohol use, ranging from mild (e.g., hangovers, missed classes) to severe (e.g., assault, even death). Online interventions targeting alcohol use among college students reduce alcohol consumption and associated problems. These interventions are popular among colleges because they are relatively inexpensive and easily disseminated. However, online interventions are not as efficacious as face-to-face interventions, such as brief motivational interviews. The proposed project employs emailed boosters in a randomized, controlled trial in an effort to improve the efficacy an existing, popular, free online intervention, while at the same time maintaining low cost and easy dissemination. Adding boosters after interventions is a common technique to improve the efficacy of the original intervention. Boosters have been used successfully for alcohol use interventions among those seeking injury treatment in emergency medical settings. However, prior research has not supported booster efficacy for college student alcohol interventions. The current project develops and evaluates the effectiveness of boosters for a widely-used college student alcohol intervention. Specifically, the present project improves boosters by providing easy access via email; providing succinct, personalized feedback; and providing reminders of protective behavioral strategies. To test the effectiveness of adding boosters, participants randomized to alcohol-intervention-plus-boosters receive emails 2 weeks after the intervention with tailored feedback based upon their reported alcohol consumption. Participants are assessed up to nine months. The current research addresses the following specific aims: Aim 1: Improve the efficacy of an easily-disseminated computerized intervention by adding personalized follow-up boosters, where efficacy is evidenced by reduced drinking and negative alcohol-related consequences (i.e., stronger effect sizes in the booster group immediately after receiving the booster). Aim 2: Extend the duration of the reduction in drinking and associated problems through the use of these personalized follow-up boosters (i.e., significant differences between the booster and control groups at later timepoints). Aim 3: Examine protective behavioral strategies highlighted by the booster as mediating behavioral mechanisms of change.

Eligibility Criteria

Inclusion Criteria

  • Current college students at the sponsor institution at the time of enrollment
  • Between the ages of 18 and 24
  • Consumed at least standard drink of alcohol in the past 2 weeks

Exclusion Criteria

  • Under age of 18
  • Over age of 24
  • Not a college student
  • Did not drink alcohol in the past 2 weeks
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03433794). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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