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N/A N=352 Randomized Single-blind Treatment

Brief Alcohol E-Interventions Study

Alcohol Drinking in College

Enrolled (actual)
352
Serious AEs
0.0%
Results posted
Jun 2019
Primary outcome: Primary: Mean Drinks Per Day — .93; 1.15; .86; 1.38 Drinks per day — p=<.05

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Brief Tablet-based Intervention to Address Heavy Alcohol Use (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Wayne State University
Primary completion
Sep 2017

Outcome Measures

OutcomeResultp-value
PRIMARY
Mean Drinks Per Day
.93; 1.15; .86; 1.38; 1.09; 1.17 <.05 sig
SECONDARY
Number of Heavy Drinking Days Per Month
1.86; 2.00; 1.52; 2.05; 2.36; 2.19 <.05 sig
SECONDARY
Report of Alcohol Related Consequences
5.24; 3.91; 3.95; 4.41; 5.23; 4.00 <.05 sig
SECONDARY
Intention to Reduce Alcohol Use
6.18; 6.68; 7.48; 8.41; 10.09; 9.29 <.05 sig

Summary

The project seeks to develop an effective computer-delivered brief intervention to reduce alcohol use using the Multiphase Optimization Strategy (MOST). Sixteen different versions of the intervention will be tested with manipulation of common factors (empathy & positive regard), use of a voice, and use of an animated narrator. Participants will include 352 undergraduate students randomly assigned to one intervention condition; follow-up assessments will take place at one and 3 months. The main outcome will be means drink per day over the past 30 day.

Eligibility Criteria

Inclusion Criteria

Participants must be students at Wayne State University, aged 18 or older. Additionally, participants must report either (1) consuming 3 (women)/4 (men) drinks per day or 7 (women)/14 (men) drinks per week, (2) getting drunk at least once per week over the past 6 months or (3) binge drinking at least once per week over the past 6 months (i.e. more than 4 (women)/5 (men) drinks in a 2 hr. period).

Exclusion Criteria

Individuals who are under the age of 18, or who do not meet the study's drinking criteria

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02952872). 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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