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Completed

NCT Number: NCT01688245

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

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

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Key information

Age range

18 year–25 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Pittsburgh Medical Center-Mercy Hospital

Pittsburgh, Pennsylvania, 15221, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

SMS assessments & feedback

Behavioral

Weekly pre-weekend drinking plan and post-weekend drinking outcome assessments with personlaized feedback

SMS Assessments

Behavioral

Weekly post-weekend drinking outcome assessments

Primary outcomes

  1. Timeline Follow-back Procedure

    Time frame: 30 Days

Secondary outcomes

  1. Injury Behavior Checklist

    Time frame: 3 months

Sponsors and collaborators

Lead sponsor

University of Pittsburgh

Other

Registry information

Acronym: TRAC

Important dates

Study start
2012
Primary completion
2014
Study completion
2015
First posted
Sep 19, 2012
Registry last updated
May 27, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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