RECRUITING

Cannabis Observations on Brain Waves, Retrieval, and Attention: Experiment 3

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This study investigates the impact of ∆9-tetrahydrocannabinol (THC) and cannabidiol (CBD) on recognition memory in healthy, regular cannabis users. Participants complete the same recognition memory task after self-administering one of two different strains of cannabis flower one day and while not intoxicated another day. Event-related potentials (ERPs) are measured via electroencephalogram (EEG) during the recognition memory task. Blood is collected to quantify THC and CBD exposure. Participants also complete self-report measures of medical history, sleep quality, subjective cognitive function, physical activity, psychological functioning, substance use, and acute drug effects.

Official Title

Cannabis Observations on Brain Waves, Retrieval, and Attention: Experiment 3 (COBRA)

Quick Facts

Study Start:2024-10
Study Completion:2026-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06669585

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:21 Years to 40 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Must be between the ages of 21 and 40 and provide informed consent;
  2. 2. Must be right-handed (Laterality Quotient \> 60 on Edinburgh Handedness Inventory - Short Form);
  3. 3. Must use cannabis at least 4 days during the month;
  4. 4. Must be a cannabis user for at least a year;
  5. 5. Must self-report not using other illicit recreational drugs (e.g., cocaine, benzodiazepines (non-prescription), opiates (non-prescription), MDMA, sedatives, or methamphetamine) in the past 30 days, during the Pre-Screening;
  6. 6. Must not test positive on a urine toxicology test for drugs of abuse at the Baseline appointment;
  7. 7. Must not be using psychotropic medications, however anti-depressant, non-benzodiazepine anti-anxiety, and ADHD medications are ok. ADHD medication users must be willing to abstain from ADHD medication use on appointment days;
  8. 8. Must not be a regular nicotine user (≤4 days per week; cigarette, E-cigs, or smokeless);
  9. 9. Must not have used caffeine or nicotine (cigarette, E-cigs, or smokeless) for 4 hours before each appointment;
  10. 10. Must have a breath alcohol level of 0 at Baseline appointment (to sign consent form);
  11. 11. Must not be actively seeking or in treatment for any substance use disorder;
  12. 12. Female subjects must not be or trying to become pregnant (as indicated by a pregnancy test administered at Baseline appointment);
  13. 13. Must not be in treatment for psychotic disorder or bipolar disorder; or have a history with these disorders;
  14. 14. Must not have any physical characteristics (e.g., thick hair, head size exceeding the limit of the net, dyed hair) or experience any technical difficulties during testing that result in a poor-quality EEG recording.
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Katie N Paulich, PhD
CONTACT
3034929549
cobra.custudy@gmail.com

Principal Investigator

Timothy Curran, PhD
PRINCIPAL_INVESTIGATOR
University of Colorado, Boulder

Study Locations (Sites)

Center for Innovation and Creativity (CINC)
Boulder, Colorado, 80301
United States

Collaborators and Investigators

Sponsor: L. Cinnamon Bidwell

  • Timothy Curran, PhD, PRINCIPAL_INVESTIGATOR, University of Colorado, Boulder

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-10
Study Completion Date2026-01

Study Record Updates

Study Start Date2024-10
Study Completion Date2026-01

Terms related to this study

Keywords Provided by Researchers

  • Cannabis
  • Memory
  • Electroencephalography

Additional Relevant MeSH Terms

  • Cannabis
  • Memory
  • Electroencephalography