Condition: Alcohol Drinking · Alcohol Intoxication · Sponsor: University of Illinois at Urbana-Champaign
The study will employ a combined laboratory-ambulatory design. Participants will engage in ambulatory assessment over the course of 14 days, wearing biosensors assessing transdermal alcohol concentration (TAC) and providing breathalyzer readings in real-world contexts. Also during this period, participants will attend three laboratory alcohol-administration sessions scheduled at one-week intervals, with alcohol dose and rate of consumption manipulated within and between participants, respectively. Laboratory visits will also double as ambulatory orientation, check-in, and close-out sessions.
This description comes directly from the study's public registry record.
Catharine Fairbairn, PhD · 217-300-5850 · uiucalcohollab@gmail.com
Always discuss trial participation with your own doctor first.
| University of Illinois at Urbana-Champaign | Champaign, Illinois, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT05692830