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Distinguishing Alcohol Intoxication, Cannabis Intoxication and Co-intoxication Using Electroencephalography (EEG)

Not Applicable
Recruiting
Conditions
Alcohol Use, Unspecified
Cannabis Use
Registration Number
NCT06259916
Lead Sponsor
Colorado State University
Brief Summary

This is a randomized, parallel-group study designed to explore the differences between cannabis intoxication, alcohol intoxication and co-intoxication involving both alcohol and cannabis, utilizing electroencephalography (EEG) as well as more traditional intoxication measures such as breath alcohol concentration and balance metrics. If eligible for the study, participants will be randomized to complete one study session in our mobile laboratory, during which they will use either alcohol, cannabis (which will be self-administered, ad libitum) or both alcohol and cannabis.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
99
Inclusion Criteria
  • 21-50 years old
  • Heavy drinkers (consuming more than 4 drinks/day or more than 14 drinks/week for men, or more than 3 drinks/day or more than 7 drinks/week for women)
  • Regular users of legal-market flower cannabis (at least 2x/week in past 3 months)
  • report simultaneously using alcohol and legal-market flower cannabis at least once per month in the past 3 months
  • English speakers.
Exclusion Criteria
  • Daily tobacco users
  • Diagnosed with or seeking treatment for alcohol use disorder (AUD) or other substance use disorder (SUD)
  • Females cannot be pregnant, breastfeeding or trying to become pregnant
  • Meet criteria for psychotic, bipolar or major depressive disorder with suicidal ideation, or history of these disorders, 5) Current use of psychotropic (except anti-depressants)
  • Report illicit drug use in past 60-days or fail drug screen on the day of the study appointment
  • Major medical condition contraindicating alcohol and/or cannabis consumption.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Electroencephalography (EEG) Objective Cognitive Function Measures--Amplitude (microvolts)Immediately pre-substance use, 1-hour post-use, 2-hours post-use, 4-hours post-use

The EEG amplitude (measured in microvolts) will be obtained while participants perform the speeded visual flanker task

Electroencephalography (EEG) Objective Cognitive Function Measures--Latency (milliseconds)Immediately pre-substance use, 1-hour post-use, 2-hours post-use, 4-hours post-use

The EEG latency (measured in milliseconds) will be obtained while participants perform the speeded visual flanker task

Standing postural stabilityImmediately pre-substance use, 1-hour post-use, 2-hours post-use, 4-hours post-use

An iPod Touch will be attached to each participant's hip with a simple elastic/Velcro strap. An app on the device will record fine grained movements while they try to stand as still as possible for 30-60 seconds under four conditions that vary in terms of demand on the proprioceptive system (eyes open, eyes closed), and on a stable vs. soft (foam) surface.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Colorado State University

🇺🇸

Fort Collins, Colorado, United States

Colorado State University
🇺🇸Fort Collins, Colorado, United States
Hollis C. Karoly, PhD
Principal Investigator

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