Status:

COMPLETED

Reactions to E-cigs and Alcohol

Lead Sponsor:

Indiana University

Collaborating Sponsors:

National Institute on Alcohol Abuse and Alcoholism (NIAAA)

Conditions:

Alcohol Abuse

Nicotine Dependence Tobacco Product

Eligibility:

All Genders

21+ years

Phase:

NA

Brief Summary

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 consumpti...

Detailed Description

Participants will be recruited via study fliers and notices in the community and via word-of-mouth. After viewing study advertisements, participants will call the lab and complete an over the phone sc...

Eligibility Criteria

Inclusion

  • 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)

Exclusion

  • 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

Key Trial Info

Start Date :

March 24 2017

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

November 11 2018

Estimated Enrollment :

35 Patients enrolled

Trial Details

Trial ID

NCT03449017

Start Date

March 24 2017

End Date

November 11 2018

Last Update

November 29 2018

Active Locations (1)

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Indiana Univerisity Purdue University Indianapolis

Indianapolis, Indiana, United States, 46202