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Study identifier: NCT05576350 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

TRAC-ER Intervention to Reduce Risky Alcohol Use and HIV Risk

Condition: Risk Behavior · Alcohol Use Disorder · HIV Infections  ·  Sponsor: University of Kentucky

PhaseNA
Planned participants405
Who can joinAll sexes, 18 Years to 35 Years
Healthy volunteersYes

About this study

Ecological momentary interventions (EMI), which use phones to deliver messages to reduce alcohol use and related risk behaviors during or prior to drinking events, can help to address triggers in real-time. GPS tracking can determine when individuals visit places they have previously reported drinking or triggers to drink and then EMI messages can be delivered upon arrival to prevent risky alcohol use. A mobile app has been developed that uses GPS tracking to determine when individuals visit "risky" places and then delivers a survey asking what behaviors they engaged in while at the location. The goal of the proposed study is to use this app to enhance the Tracking and Reducing Alcohol Consumption (TRAC) intervention by delivering messages that encourage participants to employ strategies discussed during TRAC sessions when arriving at risky places. When they leave these places, they will complete a survey and breathalyzer reading in order to collect event-level self-report and biological data on alcohol use and HIV risk. If their breathalyzer result indicates alcohol use, they will receive harm reduction messaging. It is expected that combining TRAC with EMI ("TRAC-ER") will increase effectiveness by reinforcing topics discussed during these sessions, providing in-the-moment messaging to address triggers, and collecting real-time alcohol use data.

This description comes directly from the study's public registry record.

Talk to the study team

Carolyn Lauckner, PhD  ·  859-562-3335  ·  carolyn.lauckner@uky.edu

Always discuss trial participation with your own doctor first.

Locations (2)

Yale UniversityNew Haven, Connecticut, United StatesRecruiting
University of KentuckyLexington, Kentucky, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05576350