ClinicalTrials.gg
CompletedNCT03433794Updated Dec 1, 2020Results posted

Alcohol Health Education Among College Drinkers

A Phase 1 interventional study of Alcohol 101 Plus (TM) and Booster in College Student Drinking, sponsored by Abby Braitman. Completed. Open to participants aged 18 Years to 24 Years. Per ClinicalTrials.gov, last updated 2020-12-01.

Sponsored by Abby Braitman · Phase 1, Interventional, and Treatment

From the registry’s dates

  • Registered 5 years after the study started (first participant enrolled Jan 2013, registered Feb 2018).

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Phase
Phase 1
Study type
Interventional
Enrollment
537
Allocation
Randomized
Ages
18 Years to 24 Years
Sex
All
01

Study 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.

Read the detailed description

Alcohol use within the college student population 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). College student alcohol use is a significant problem, and reducing consumption and associated problems is a priority among researchers, educators, and mental health professionals who work with this population.

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 current project employs emailed boosters in a randomized, controlled trial in an effort to improve the efficacy an existing, popular, free online intervention, Alcohol 101 Plus (TM), 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 improved the efficacy or effect duration for interventions targeting smoking cessation, mammograms, dating violence, caregiver skills, binge eating, and many other behaviors. Boosters have been used successfully for alcohol use interventions among those seeking injury treatment in emergency medical settings. Despite these successes, 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 by improving on the design of boosters. Specifically, the present project improves boosters by providing easy access via email to minimize burden; providing succinct, personalized feedback; and providing reminders of protective behavioral strategies. To test the effectiveness of adding boosters, participants randomized to the alcohol-intervention-plus-boosters condition receive emails 2 weeks after the intervention with tailored feedback based upon their reported alcohol consumption. Participants are initially assessed biweekly, then every three months 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 after the significant differences between the intervention-only and control groups erode).

Aim 3: Examine protective behavioral strategies highlighted by the booster as mediating behavioral mechanisms of change.

3A: Determine if increased exposure to protective strategies through an emailed booster results in increased use of these strategies.

3B: Determine if those who increase their use of protective behavioral strategies decrease their alcohol consumption and related problems they experience.

3C: Assess the combination of these two effects (i.e., the indirect effect). The proposed study will be a critical first step to adapt existing online interventions. The findings from this study will be used to identify implications for modifying the protocol or booster.

02

Conditions studied

  • College Student Drinking
03

In context

Alcohol Drinking in College

38 studies on the registry are indexed under Alcohol Drinking in College; 8 are open to participants now.

This study's enrollment of 537 is above the median of 258 across 36 interventional studies indexed under Alcohol Drinking in College.

Browse Alcohol Drinking in College studies →

Lead sponsor

Abby Braitman is the lead sponsor of 5 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 24 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

Exclusion Criteria:

  • Under age of 18
  • Over age of 24
  • Not a college student
  • Did not drink alcohol in the past 2 weeks
05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
537 participants (actual)

Study arms

  • Placebo comparator
    Control

    The control group spent 60 minutes on an online education session (Lilly for Better Health) directed at other health behaviors besides alcohol. The site provides practical tips on general well-being such as healthy eating, physical activity, and stress management, as well as provides information on managing health conditions such as diabetes, heart disease and depression. Their email 2 weeks later contained only a reminder to participate in follow-up surveys.

    Behavioral: Lilly for Better Health

  • Active comparator
    Intervention Only

    Participants navigated through Alcohol 101 Plus (TM) for 60 minutes. This is an online intervention, free to institutions and individuals. It is a combination of several intervention components, including alcohol education, personalized feedback, attitude-focused strategies, and skills training. It also included a virtual bar, where participants provide basic information such as sex, weight, and state of residence so that the program can provide tailored information on blood alcohol content (BAC) as well as state regulations regarding legal limits. Their email 2 weeks later contained only a reminder to participate in follow-up surveys.

    Behavioral: Alcohol 101 Plus (TM)

  • Experimental
    Intervention-plus-Booster

    Participants navigated through Alcohol 101 Plus (TM) for 60 minutes. This is an online intervention, free to institutions and individuals. It is a combination of several intervention components, including alcohol education, personalized feedback, attitude-focused strategies, and skills training. It also included a virtual bar, where participants provide basic information such as sex, weight, and state of residence so that the program can provide tailored information on blood alcohol content (BAC) as well as state regulations regarding legal limits. Importantly, their email 2 weeks later contained a reminder to participate in follow-up surveys, plus personalized feedback based on participant reported perceived alcohol norms, actual alcohol norms, and reported harm reduction strategies.

    Behavioral: Alcohol 101 Plus (TM) · Behavioral: Booster

Interventions

  • BehavioralAlcohol 101 Plus (TM)

    It is a combination of several intervention components, including alcohol education, personalized feedback, attitude-focused strategies, and skills training. It also included a virtual bar, where participants provide information such as sex, weight, and state so that the program can provide tailored information on blood alcohol content (BAC) as well as state regulations regarding legal limits. The program provides updated BACs based upon choices about what to consume and how quickly to consume it. The intervention is highly interactive, with text, photos, videos, and narratives for fictional students with decision points where the participant chooses what the fictional student should do. It is a non-linear environment, where participants choose which sections of the website to explore.

  • BehavioralBooster

    Personalized feedback was emailed to participants. Content included sex-specific descriptive normative information (i.e., drinks per week typically consumed by males and females at the same institution), as well as reminders of harm reduction strategies (i.e., techniques the participant reported using in their last survey, versus techniques not used).

    Also known as: Personalized Normative Feedback

  • BehavioralLilly for Better Health

    This is an online education session directed at other health behaviors besides alcohol. The site provides practical tips on general well-being such as healthy eating, physical activity, and stress management, as well as provides information on managing health conditions such as diabetes, heart disease and depression. It was not expected to influence alcohol use.

06

What researchers measure

Primary outcomes

  1. Alcohol Consumption

    Participant self-reported number of standard drinks consumed by participant over the past 2 weeks

    Time frame: Past 2 weeks, reported at Baseline assessment (pre-intervention)

Secondary outcomes

  1. Alcohol-related Consequences

    Participant self-report on the Young Adult Alcohol Consequences Questionnaire (YAACQ; Read, Kahler, Strong, \& Colder, 2006), which assesses alcohol-related problems experienced by the participant. Total scores are created by summing all individual items, and range from 0 to 48, with higher values representing more problems experienced (i.e., worse outcomes).

    Time frame: Past 2 weeks, reported at Baseline assessment (pre-intervention)

07

Results

Posted Aug 10, 2020

Participant flow

Baseline
Participant flow — Baseline
MilestoneControlIntervention OnlyIntervention-plus-Booster
Started183173181
Completed183173181
Not completed000
2-Week Assessment
Participant flow — 2-Week Assessment
MilestoneControlIntervention OnlyIntervention-plus-Booster
Started183173181
Completed117112109
Not completed666172
4-Week Assessment
Participant flow — 4-Week Assessment
MilestoneControlIntervention OnlyIntervention-plus-Booster
Started183173181
Completed989591
Not completed857890
6-Week Assessment
Participant flow — 6-Week Assessment
MilestoneControlIntervention OnlyIntervention-plus-Booster
Started183173181
Completed948580
Not completed8988101
3-Month Assessment
Participant flow — 3-Month Assessment
MilestoneControlIntervention OnlyIntervention-plus-Booster
Started183173181
Completed697371
Not completed114100110
6-Month Assessment
Participant flow — 6-Month Assessment
MilestoneControlIntervention OnlyIntervention-plus-Booster
Started183173181
Completed655850
Not completed118115131
9-Month Assessment
Participant flow — 9-Month Assessment
MilestoneControlIntervention OnlyIntervention-plus-Booster
Started183173181
Completed495239
Not completed134121142

Outcome measures

PrimaryAlcohol Consumption

Participant self-reported number of standard drinks consumed by participant over the past 2 weeks

Time frame:
Past 2 weeks, reported at Baseline assessment (pre-intervention)
Reported as:
Mean · drinks
Alcohol Consumption
drinksControlIntervention OnlyIntervention-plus-Booster
Alcohol Consumption16.929 ± 14.82617.988 ± 16.87018.039 ± 16.382
SecondaryAlcohol-related Consequences

Participant self-report on the Young Adult Alcohol Consequences Questionnaire (YAACQ; Read, Kahler, Strong, \& Colder, 2006), which assesses alcohol-related problems experienced by the participant. Total scores are created by summing all individual items, and range from 0 to 48, with higher values representing more problems experienced (i.e., worse outcomes).

Time frame:
Past 2 weeks, reported at Baseline assessment (pre-intervention)
Reported as:
Mean · problems
Alcohol-related Consequences
problemsControlIntervention OnlyIntervention-plus-Booster
Alcohol-related Consequences6.656 ± 5.5667.156 ± 6.0667.011 ± 6.367

Adverse events

Non-serious events are listed at a 0% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Control0/183 (0%)0/183 (0%)0/183 (0%)
Intervention Only0/173 (0%)0/173 (0%)0/173 (0%)
Intervention-plus-Booster0/181 (0%)0/181 (0%)0/181 (0%)

Baseline characteristics

Age, Continuous
Age, Continuous(years)ControlIntervention OnlyIntervention-plus-BoosterTotal
Mean19.792 ± 1.77919.792 ± 1.72619.370 ± 1.47619.650 ± 1.674
Sex: Female, Male
Sex: Female, Male(Participants)ControlIntervention OnlyIntervention-plus-BoosterTotal
Female122116124362
Male615757175
Race/Ethnicity, Customized
Race/Ethnicity, Customized(Participants)ControlIntervention OnlyIntervention-plus-BoosterTotal
Caucasian or White829288262
African-American or Black745968201
Asian or Pacific Islander118625
Native American1034
Other10101434
Hispanic24181355
non-Hispanic158154167479
Region of Enrollment
Region of Enrollment(participants)ControlIntervention OnlyIntervention-plus-BoosterTotal
United States183173181537
08

Study locations

No study locations are listed for this record.

09

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

10

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Jan 2013 to primary completion in Sep 2014, 19 months.

Results were first posted in Aug 2020, 5 years 11 months after primary completion.

How these figures are worked out, and which studies are left out of them.

Registered
Feb 8, 2018
First posted
Feb 15, 2018
StartActual
Jan 29, 2013
Primary completionActual
Sep 10, 2014
CompletionActual
Sep 10, 2014
Results first posted
Aug 10, 2020
Last update
Dec 1, 2020
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Dec 1, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
11

Registry details

Key details

Study ID
NCT03433794
Lead sponsor
Abby Braitman
Responsible party
Abby Braitman (Research Assistant Professor, Old Dominion University) — Sponsor-investigator
First posted
Feb 15, 2018
Start date
Jan 29, 2013
Primary completion
Sep 10, 2014
Completion
Sep 10, 2014
Results posted
Aug 10, 2020
Last update
Dec 1, 2020

Study contacts

Abby L Braitman, Ph.D.
principal investigator · Old Dominion University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Nov 2020. You cannot join it, but the record below documents what was studied.

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