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Clinical Trials/NCT01688245
NCT01688245CompletedNot Applicable

A Text Message Behavioral Intervention to Reduce Alcohol Consumption in Young Adults

University of Pittsburgh2 sites in 1 country765 target enrollmentStarted: November 2012Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
765
Locations
2
Primary Endpoint
Timeline Follow-back Procedure

Study Overview

Brief Summary

Investigators aim to test the effectiveness of a text-message-based behaivoral intervention in reducing binge drinking among young adults.

Detailed Description

Alcohol consumption, especially in the form of heavy episodic drinking (bingeing), is common among young adults. Despite high rates of illness and injury associated with heavy episodic drinking, many young adults are not aware of the risks, few seek help for their drinking and many at-risk are not exposed to prevention-based intervention. Opportunistic screening in hospital Emergency Departments (EDs) tied to behavioral interventions has the potential to prevent future alcohol-related harm among young adults, but efficacy across outcomes has been mixed and large-scale implementation of prevention programs is low. Given the rapidly growing use of cell phone text-messaging (SMS) as a primary form of communication among young adults, SMS could be used to deliver health prevention interventions. We will recruit young adults identified in the ED with hazardous drinking behavior in a 3-arm randomized controlled trial to test the hypothesis that exposure to a 12-week SMS program will result in immediate (3-month) and lasting (6-, and 9-month) decreases in alcohol consumption.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Double (Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 25 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • AUDIT-C score 3 or more for women and 4 or more for men

Exclusion Criteria

  • Current treatment for psychiatric disease
  • Any prior treatment for drug or alcohol use disorder

Outcomes

Primary Outcomes

Timeline Follow-back Procedure

Time Frame: 30 Days

Secondary Outcomes

  • Injury Behavior Checklist(3 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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