Alcohol and Cannabis Concentrates Co-Administration

Sponsor
Colorado State University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05999344
Collaborator
Institute of Cannabis Research (ICR)--Colorado State University, Pueblo (Other)
80
1
1
31.5
2.5

Study Details

Study Description

Brief Summary

The goal of this study is to learn about the effects of combining alcohol with cannabis concentrate products which contain high levels of THC. The main question[s] it aims to answer are, 1) How does the order in which someone consumes THC and alcohol in a given co-use session impact outcomes such as blood alcohol level, heart rate or subjective drug effects, and 2) how does THC percentage in cannabis influence outcomes following alcohol and cannabis co-administration. Participants will be scheduled for our mobile lab to come to their residence. During the session, they will:

  • consume a standardized dose of alcohol as well as use their own preferred cannabis concentrate product.

  • they will then remain in our mobile lab for about 4 hours and complete some surveys as well as do some cognitive tasks on an iPad every 30 minutes.

  • They will also have their blood drawn three times throughout the session, and will periodically be asked to blood into a breathalyzer to measure blood alcohol level.

Researchers will compare people who use alcohol prior to cannabis to those who use cannabis prior to alcohol to determine whether order of use impacts outcomes.

Condition or Disease Intervention/Treatment Phase
  • Other: commercially available cannabis and commercially available alcohol
N/A

Detailed Description

Individuals who drink alcohol commonly report co-using cannabis, and the increasing availability of new formulations of highly potent cannabis products on the legal market means that alcohol is likely being combined with cannabis products that contain high levels of delta-9-tetrahydrocannabinol (THC). There is limited existing research on the acute effects of cannabis products containing high amounts of THC, such as cannabis concentrates, which often contain up to 90% THC. Existing laboratory data suggests that consuming alcohol and cannabis together (compared to alcohol alone) is associated with reduced BAC, delayed time to peak blood alcohol concentration (BAC), longer duration of intoxication, and increased subjective intoxication, but it is unknown how cannabis concentrates may interact with alcohol to influence these outcomes. There is also a lack of research regarding whether timing or order of use matters, though recent survey data from our group and others suggests that using alcohol before cannabis may confer additional risk compared to using cannabis prior to alcohol. The present study leverages a federally-compliant mobile laboratory design to explore the acute effects of self-administered cannabis concentrates alongside a standardized dose of alcohol. The investigators will recruit a community sample of individuals who regularly use alcohol and cannabis to participate study sessions in our mobile laboratory. The sessions will involve individuals consuming cannabis concentrates of their choice (that they acquire themselves) along with a standardized dose of alcohol. Half of the participants will use the alcohol before cannabis, and the other half will use the cannabis before alcohol. The investigators will measure intoxication and biological outcomes every 30 minutes for 4 hours. The investigators will also measure differences between those who used alcohol before cannabis and those who used cannabis before alcohol.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
80 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
Single group, randomized order of administrationSingle group, randomized order of administration
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Exploring Intoxication During Acute Alcohol and Cannabis Concentrate Co-Administration: A Focus on Cannabinoid Content and Order Effects
Actual Study Start Date :
Dec 16, 2021
Anticipated Primary Completion Date :
Aug 1, 2024
Anticipated Study Completion Date :
Aug 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Alcohol + Cannabis

Participants are randomly assigned to receive the standardized alcohol dose during the experimental session prior to going inside their residence to self-administer their preferred cannabis concentrate product or randomly assigned to going inside their residence to self-administer their preferred cannabis concentrate product and then receive the standardized alcohol dose. All participants receive alcohol and cannabis, however, the order of ingestion is randomly assigned.

Other: commercially available cannabis and commercially available alcohol
Self administration of cannabis and researcher administered alcohol

Outcome Measures

Primary Outcome Measures

  1. Breath Alcohol Level (BrAC) [Baseline (pre ingestion) and every 30 minutes (post ingestion) for a total of 270 minutes (9 measures)]

    Breath alcohol level will be measured using a breathalyzer repeatedly during the experimental session

  2. Alcohol Urge Questionnaire (AUQ) [Baseline (pre ingestion) and every 30 minutes (post ingestion) for a total of 270 minutes (9 measures)]

    The AUQ is a self-report measure of urge for alcohol and has been validated for real-time assessment of alcohol craving in the laboratory. The total score on the measure ranges from 0-48 where higher is worse

  3. Heart Rate (HR) [Baseline (pre ingestion) and every 30 minutes (post ingestion) for a total of 270 minutes (9 measures)]

    Heart rate (beats per minute) is measured using a finger pulse oximeter

  4. ARCI Marijuana Scale [Baseline (pre ingestion) and every 30 minutes (post ingestion) for a total of 270 minutes (9 measures)]

    The ARCI scale measures subjective responses to cannabis. total score ranges from 0-12 where higher is worse

  5. DRUID Psychomotor Battery [Baseline (pre ingestion) and every 30 minutes (post ingestion) for a total of 270 minutes (9 measures)]

    The DRUID is a mobile app that tests for cognitive and motor impairment, and has been shown to detect impairment related to alcohol and cannabis use. total score ranges from 0-100 where higher is worse.

Secondary Outcome Measures

  1. Blood-THC [Blood is drawn immediately prior to alcohol and cannabis consumption, again 60 minutes post alcohol administration start time, and again 240 minutes post alcohol start time]

    We will quantify levels of THC in the blood before and after the participant uses their cannabis product

  2. Biphasic Effects of Alcohol Scale (BAES) [Baseline (pre ingestion) and every 30 minutes (post ingestion) for a total of 270 minutes (9 measures)]

    The BAES measures the stimulating and sedating effects of alcohol and is validated for use in laboratory settings. This scale produces a stimulation subscale (total score ranges from 0-70 where higher is more stimulated) and a sedation subscale (total score ranging from 0-70 where higher is more sedated)

  3. Profile of Mood States (POMS) [Baseline (pre ingestion) and every 30 minutes (post ingestion) for a total of 270 minutes (9 measures)]

    The POMS is a self-report rating scale that assesses state-level, distinct mood states. The POMS produces multiple subscales (Tension, depression, anger, fatigue, confusion, vigour, as well as a total mood disturbance scale)

Eligibility Criteria

Criteria

Ages Eligible for Study:
21 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  1. 21-65 years old,

  2. Heavy drinkers (for men, >4 drinks in one occasion, or >14 drinks per week; for women,

3 drinks in one occasion, or >7 drinks per week)

  1. Regular users of legal-market cannabis (at least 3x/week in past 3 months)

  2. Have experience using cannabis concentrates within the last year

  3. Willing to obtain a concentrate product of their choice for use in the study.

Exclusion Criteria:
  1. Diagnosed with or seeking treatment for alcohol use disorder (AUD) or other substance use disorder (SUD)

  2. Pregnant, breastfeeding or trying to become pregnant

  3. Meet criteria for psychotic, bipolar or major depressive disorder with suicidal ideation, or history of these disorders

  4. Current use of psychotropic (except anti-depressants) or steroid medications

  5. Report illicit drug use in past 60-days or fail drug screen (drug screen tests for the presence of amphetamines, benzodiazepines, cocaine, THC, methamphetamine and opioids; only THC is allowed to be present in urine in order to be eligible to participate in the study

  6. Major medical condition contraindicating alcohol and/or cannabis consumption (e.g., liver disease, heart disease, or being told by a doctor that it is unsafe to consume alcohol or cannabis due to a medical condition)

  7. Have participated in another research study in the past 8 weeks.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Colorado State University Fort Collins Colorado United States 80523

Sponsors and Collaborators

  • Colorado State University
  • Institute of Cannabis Research (ICR)--Colorado State University, Pueblo

Investigators

  • Principal Investigator: Hollis C Karoly, PhD, Colorado State University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Colorado State University
ClinicalTrials.gov Identifier:
NCT05999344
Other Study ID Numbers:
  • 2161
First Posted:
Aug 21, 2023
Last Update Posted:
Aug 24, 2023
Last Verified:
Aug 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by Colorado State University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 24, 2023