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The Drinking Dashboard Study

University of Missouri (MU) logo

University of Missouri (MU)

Status

Completed

Conditions

Alcohol Drinking

Treatments

Behavioral: Drinking Dashboard

Study type

Interventional

Funder types

Other

Identifiers

NCT05630625
2067803

Details and patient eligibility

About

This study aims to develop and pilot test the efficacy of a "Drinking Dashboard" providing participants weekly feedback on the risk factors and consequences of blackout.

Full description

Approximately 50% of young adults who drink alcohol experience alcohol-induced "blackouts," defined as permanent (en bloc) or temporary (fragmentary) memory loss for events that occurred while they are drinking. This experience of alcohol-induced blackout is associated prospectively with alcohol-related harm, including emergency room visits and sexual coercion, with medical care costs exceeding $469,000 per year. While young adults who have recently experienced a blackout report less favorable evaluations of drinking events and increased motivation to decrease their drinking, they do not actually change their drinking behavior as a result of the blackout alone. Collectively, these data suggest that blackouts may serve as an opportunity for intervention, after which young adults are more likely to respond to alcohol feedback. This R34 aims to develop an intervention tailored to individuals who experience blackouts. In the trial phase, 162 young adults (50% female, ≥50% non-college) who report a history of blackout will be randomly assigned to receive the intervention (n=81) or assessment only (n=81). Outcomes will be assessed immediately post-intervention and at 3-month follow-up.

Enrollment

169 patients

Sex

All

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 18-30 years of age
  • Binge drinking in a typical week
  • Any form of alcohol-induced memory impairment in the past month at baseline

Exclusion criteria

  • Psychiatric disorder requiring immediate clinical attention (e.g., psychosis, suicidal ideation with intent and plan)

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

169 participants in 2 patient groups

Drinking Dashboard
Experimental group
Description:
Day-level feedback on alcohol use and consequences
Treatment:
Behavioral: Drinking Dashboard
Assessment Only
No Intervention group
Description:
Daily assessment control group

Trial contacts and locations

1

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Central trial contact

Mary Beth Miller, PhD

Data sourced from clinicaltrials.gov

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