Examining the effects of cannabis on stress and inhibition in healthy adults

Cannabis and Polysubstance Use: Response Inhibition and Stress Exposure

This study is testing how different types of cannabis oil affect stress and self-control in healthy adults who use cannabis for fun.

Quick facts

• Phase: Phase 1
• Study type: Interventional
• Enrollment: 20 (estimated)
• Ages: 19 Years to 35 Years
• Sex: All
• Sponsor: University of British Columbia (Academic / other)
• Locations: 1 site (Vancouver, British Columbia)
• Trial ID: NCT05261321 on ClinicalTrials.gov

What this trial studies

This Phase I trial investigates how cannabis affects stress reactivity and inhibition in healthy adults who use cannabis recreationally. Participants will be given either high CBD:THC cannabis oil, low CBD:THC cannabis oil, or a placebo, and their responses will be measured through biological samples, neuroimaging, and psychosocial assessments. The study aims to establish a causal link between cannabinoid products and stress response mechanisms, particularly in those who also consume alcohol. The findings could provide valuable insights into the effects of commercially available cannabis products on mental health.

Who should consider this trial

Good fit: Ideal candidates are healthy adults aged 19-35 who are regular cannabis users and also consume alcohol.

Not a fit: Patients who do not use cannabis or are not within the specified age range may not benefit from this study.

Why it matters

Potential benefit: If successful, this study could provide evidence for the use of cannabis in managing stress and improving cognitive functioning.

How similar studies have performed: While there is ongoing research into cannabis effects, this specific focus on commercially available products in healthy users is relatively novel.

Eligibility criteria

Inclusion criteria:

1. Are 19-35 years old at the start of the study
2. Have used oral cannabis for non-medical purposes twice the past month (30 days)
3. Have previously used a minimum of 20mg of CBD
4. Have previously used a minimum of 5mg THC
5. Are using an effective and/or highly effective method of contraception and will continue to do so for the duration of participation in the study. Health Canada's definition of effective methods of contraception include barrier methods of contraception (e.g. male condom, female condom, cervical cap, diaphragm, contraceptive sponge). Health Canada's definition of highly effective methods of contraception includes hormonal contraceptives (e.g. combined oral contraceptives, patch, vaginal ring, injectables, and implants); intrauterine device (IUD) or intrauterine system (IUS); vasectomy and tubal ligation.
6. Females: are not undergoing alternative fertility methods, such as IVF, or otherwise trying to start a family for the duration of participation
7. Males: will not be donating sperm at some point during the duration of participation
8. Are able to provide informed consent
9. Are able to complete assessments in English
10. Are able to attend sessions according to the study schedule
11. Will provide proof of 2 doses of an approved COVID-19 vaccination

Exclusion criteria:

1. Are left-handed or ambidextrous
2. Females: are pregnant, nursing, or not on safe pregnancy protection
3. Are trying to conceive
4. Have a known or suspected allergy to cannabinoids and/or palm/coconut oil
5. Are hypersensitive to CBD and/or THC and/or have ever had an adverse reaction (an unwanted and unexpected reaction), to less than 40mg of CBD and/or 10mg THC
6. Have had an adverse reaction (unwanted, unexpected reaction or symptoms) to cannabis within last 6 months
7. Have a major physical problem/health concern, including:

   1. Liver-cirrhosis or other liver disease
   2. Diabetes
   3. Chronic illness that may increase risk for adverse reactions to cannabis
   4. Chronic pain
   5. Genetic glucuronidation disorders (e.g., Gilbert's disease)
   6. Cardiovascular disease, including ischemic heart disease with unstable angina or recent acute coronary syndrome in the last 3 months, uncontrolled arrhythmias, poorly controlled hypertension or high blood pressure (e.g., 130/80), or severe heart failure
   7. Delirium: active delirium or recent delirium \< 7 days, or at significant risk of delirium due to multiple comorbidities (e.g., very elderly, cognitive impairment, cerebrovascular disease) and contributing drugs (e.g., alcohol, stimulants, high doses of benzodiazepines, opioid, sedatives, psychoactive medications)
8. Are taking any of the following medications:

   1. Any medication that impacts the central nervous system, brain, and/or metabolic system
   2. Psychotropic medications, sedatives, and central nervous system depressants, including sleeping pills, tranquilizers, some pain medications, some allergy and cold medications, and anti-seizure medications
   3. Medications otherwise affecting the central nervous system, including amphetamines and other sympathomimetics
   4. Allergy medications (antihistamines; within 24 hours)
   5. Heart medications
   6. Blood pressure medication
   7. Steroid medications
   8. Opioids or other pain medications
   9. Anticholinergics: drugs that block acetylcholine, a chemical signal that plays a role in memory and learning.
   10. Drugs metabolized by cytochrome P450 enzymes, including amitriptyline, fentanyl, sufentanil, and alfentanil
   11. Highly protein-bound drugs, including warfarin, cyclosporine, and amphtericin
   12. Drugs metabolized by UGT enzymes, including propofol, antivirals
   13. Antiretroviral drugs
   14. Stomach acid inhibitors
   15. Antibiotics and antifungal medications
   16. Heart medications
   17. Other medications/substances interfering with CYP2C19 receptors

   i. Inhibitors: Fluvoxamine, isoniazid (INH), ritonavir ii. Inducers: Carbamazepine, phenytoin, rifampin iii. Substrates: Omeprazole (Prilosec), phenobarbital, phenytoin r. Other medications/substances interfering with CYP3A4 receptors: i. Inhibitors: Clarithromycin (Biaxin), diltiazem (Cardizem), erythromycin, grapefruit juice, itraconazole (Sporanox), ketoconazole (Nizoral), nefazodone (Serzone), ritonavir, telithromycin (Ketek), verapamil (Calan) ii. Inducers: Carbamazepine, Hypericum perforatum (St. John's wort), phenobarbital, phenytoin, rifampin iii. Substrates: Alprazolam (Xanax), amlodipine (Norvasc), atorvastatin (Lipitor), cyclosporine (Sandimmune), diazepam (Valium), estradiol (Estrace), simvastatin (Zocor), sildenafil (Viagra), verapamil, zolpidem (Ambien)
9. Other MRI contraindications (conditions that make MRI procedure inadvisable):

   a. Have implanted metal clips or wires, including: i. Implanted electronic device (e.g., pacemaker, defibrillator implanted medication infusion pump, electrical stimulator, and/or ear or eye implant) including retained wires that has been removed (e.g., pacemaker wires not attached to a pacemaker) ii. Stainless steel intrauterine device (IUD) iii. Metal in eye or orbit, or metal slivers iv. Ferromagnetic aneurysm clip v. Coil, catheter, or filter in any blood vessel vi. Orthopedic hardware (artificial joint, plate, screw, rod) vii. Shrapnel, bullets, or other metal fragments (i.e., metal in eye or orbit) viii. Artificial heart valve ix. Ear or eye implant x. Brain aneurysm clip xi. Implanted electronic device (i.e., drug infusion pump, electrical stimulator) xii. Coil, catheter, or filter in any blood vessel xiii. Surgery, medical procedure or tattoos (including tattooed eyeliner) in the last six weeks xiv. Other metallic prostheses b. Have a personal or family history of seizures c. Have any significant neurological disorder including, but not limited to: i. Any condition likely to be associated with increased intracranial pressure ii. Space-occupying brain lesion iii. Seizure iv. Cerebral aneurysm v. Parkinson's disease vi. Huntington's chorea vii. Multiple sclerosis viii. Significant head trauma with loss of consciousness for greater than or equal to 5 minutes d. Claustrophobia (i.e., feel uncomfortable in small spaces) or fear of loud, repetitive sounds, or inability to lay still. Participants will have to lie still in the confined space of the MRI scanner.
10. Work nightshifts
11. Have any diagnosed sleep disorders
12. Have dyscalculia
13. Have a neurodevelopmental disorder or cognitive impairments, including:

    1. Autism Spectrum Disorder
    2. Attention Deficit/Hyperactivity Disorder (ADHD)
14. Have schizophrenia spectrum disorder and/or history of psychosis
15. Meet criteria for potential mental health disorder in the Mini International Neuropsychiatric Interview (M.I.N.I.) Screen Version 7.0.2, except for alcohol and cannabis use disorders
16. Any diagnosed current mental health disorder and/or diagnosis of a mental health disorder within the past year
17. Have a non-correctable clinically significant sensory impairment (e.g., cannot hear well enough to cooperate with interview)

19) Are unable to attend sessions according to the study schedule 20) Have used opiates more than twice in the past 30 days

Where this trial is running

Vancouver, British Columbia

• B.R.A.I.N. Lab, Institute of Mental Health, Faculty of Medicine, University of British Columbia — Vancouver, British Columbia, Canada (Recruiting)

Study contacts

• Principal investigator: Christian G Schütz, MD PhD — University of British Columbia; British Columbia Mental Health and Substance Use Services
• Study coordinator: Christian G Schütz, MD PhD

Conditions Healthy; cannabis; cannabinoids; stress; neuroimaging; fMRI