Hingson and Howland (2002) estimated that 1,138 college students die from alcohol-related? traffic crashes annually. An additional 307 college students die annually from alcohol-related non-traffic? unintentional injuries and 500,000 college students annually sustain alcohol-related injuries (Hingson and? Howland 2002). Caffeinated alcoholic beverages target young adults with the promise that the caffeine will? counteract the sedating effects of alcohol and thus let the consumer remain alert and active longer, while? continuing to drink. If young people erroneously believe that caffeine in beer will protect them from alcohol-related? injury, then such beverages may increase mortality and morbidity in this population. Thus, it is? important to have accurate information about the extent to which such beverages affect impairment both? acutely and residually. Such information could correct misunderstandings young people have about the? relative safety of caffeinated beer and thereby reduce injury. The study could have implications for safety-sensitive? occupations as well. It is common for people to use caffeine to counteract the sedative effects of? alcohol. If, however, the alcohol and caffeine interact to yield greater impairment in next-day performance,? workers should be aware of this, particularly if their jobs have low tolerance for error. This study, to our? knowledge, will be the first to compare the acute and residual effects of caffeinated and non-caffeinated beer? on driving performance.? Objectives:
The aim of this study is to develop information about the acute and residual effects of a new? product being targeted to young adults. It is important to understand the effects of caffeinated alcoholic? beverages early on in the marketing campaign so that if they pose a greater threat to pubic health than? traditional alcoholic beverages, (1) consumers can be educated and (2) policy-making can be informed with? accurate information. We will compare the acute and residual effects on driving impairment of caffeinated? and non-caffeinated beer to each other and to placebo when participants have received sufficient alcoholic? beverage to attain a blood alcohol concentration (BAC) of .12 g%.? Study Design: We will conduct a placebo-controlled trial using a 2 X 2 mixed-model study design. The? within-subjects factor will be alcohol vs. placebo; the between-subjects factor will be caffeinated vs. noncaffeinated? beer.? Setting: The study will take place at the General Clinical Research Center at Boston Medical Center.? Participants: We will recruit 144 students from Boston area Universities.? Outcome Measures: Acute and residual driving impairment will be assessed using a driving simulator and? an objective measure of sustained attention/reaction time, the Psychomotor Vioilance Test (PVT).?

Agency
National Institute of Health (NIH)
Institute
National Center for Injury Prevention and Control (NCIPC)
Type
Injury Control Research and Demonstration Projects and Injury Prevention Research Centers (R49)
Project #
1R49CE000946-01
Application #
7178427
Study Section
National Center for Injury Prevention and Control Initial Review Group (SCE)
Program Officer
Childress, Adele M
Project Start
2006-09-30
Project End
2009-09-29
Budget Start
2006-09-30
Budget End
2009-09-29
Support Year
1
Fiscal Year
2006
Total Cost
$249,999
Indirect Cost
Name
Boston University
Department
Social Sciences
Type
Schools of Public Health
DUNS #
604483045
City
Boston
State
MA
Country
United States
Zip Code
02118