Reactions to E-cigs and Alcohol

Completed · Not applicable

Conditions studied: Alcohol Abuse, Nicotine Dependence Tobacco Product

In brief

The purpose of this study is to 1) examine cognitive acuity following e-cig use (as compared to no e-cig use), 2) examine motor coordination following beer and e-cig use (as compared to beer consumption only).

Key facts

Study ID

NCT03449017

Run by

Indiana University

People needed

35

Starts

2017-03-24

Expected to finish

2018-11-11

Last updated by the study team

2018-11-29

Who can join

Age: 21 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Healthy men and women, 21 years of age or older
• Regular alcohol use (reports at least one drink weekly - acceptability of average alcohol consumption will be made on a case by case basis by the PI)
• No current/prior severe alcohol or substance use disorder (endorsement of > 6 Alcohol/Drug Use history items on the phone screen)
• Current e-cigarette use (reports at least weekly use - acceptability of average e-cig use will be made on a case by case basis by the PI)
• Able to understand questionnaires/procedures in English
• Reports drinking beer (Yes/No on phone screen)

You may not qualify if…

• Pregnant/breast-feeding women (assessed via phone screen and urine screen)
• Unstable or significant medical disorders that may influence study outcome or participant safety as determined by Melissa Cyders (e.g., liver condition)
• Current/prior severe alcohol use disorder, current/prior severe substance use disorder (endorsement of > 6 Alcohol/Drug Use history items on the phone screen)
• Positive urine drug screen for amphetamines/meth-amphetamines, barbiturates, benzodiazapines, cocaine, opiates, or PCP [1-phenylcyclohexyl]
• Current mental health problems, such as depression, anxiety, post-traumatic stress disorder, bipolar disorder, or schizophrenia (self-reported at phone screen)
• Positive BrAC reading at the start of any study visit
• Court-mandated order to not drink alcohol
• Any condition that, in the judgment of the PI, could place the participant at risk or affect data validity

Where it is running

• Indiana Univerisity Purdue University Indianapolis — Indianapolis, Indiana, United States

Full record on ClinicalTrials.gov

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