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Cannabis and Polysubstance Use: Response Inhibition and Stress Exposure (CAPU RISE)

Primary Purpose

Healthy

Status
Recruiting
Phase
Phase 1
Locations
Canada
Study Type
Interventional
Intervention
Cannabis oil with a high ratio of THC to CBD
Cannabis oil with a high ratio of CBD to THC
Placebo
Sponsored by
University of British Columbia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Healthy focused on measuring cannabis, cannabinoids, stress, neuroimaging, fMRI

Eligibility Criteria

19 Years - 35 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion criteria:

  1. Are 19-35 years old at the start of the study
  2. Have used cannabis for non-medical purposes at least once per week for the past month (30 days), including at least 2 times via oral route of administration
  3. Have previously used a minimum of 20mg of CBD
  4. Have previously used a minimum of 5mg THC
  5. Meet criteria for heavy drinking:

    1. Males and intersex: ≥5 drinks on at least one occasion per month in the past 12 months
    2. Females: ≥4 drinks on at least one occasion per month in the past 12 months
  6. 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.
  7. Females: are not undergoing alternative fertility methods, such as IVF, or otherwise trying to start a family for the duration of participation
  8. Males: will not be donating sperm at some point during the duration of participation
  9. Are able to provide informed consent
  10. Are able to complete assessments in English
  11. Are able to attend sessions according to the study schedule
  12. 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

Sites / Locations

  • B.R.A.I.N. Lab, Institute of Mental Health, Faculty of Medicine, University of British ColumbiaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Placebo Comparator

Arm Label

Cannabis oil with a high ratio of THC to CBD

Cannabis oil with a high ratio of CBD to THC

Placebo

Arm Description

Participants will be given a single dose of oral cannabis oil containing 5mg THC and 0.17mg CBD.

Participants will be given a single dose of oral cannabis oil containing 5mg THC and 25mg CBD.

Participants will be given a single dose of 1 mL placebo (carrier oil with botanical terpenes) via oral route of administration.

Outcomes

Primary Outcome Measures

Change in stress response across conditions
Indicated by differences in blood-oxygenation-level-imaging (BOLD) response via functional magnetic resonance imaging (fMRI), salivary stress molecule levels (eg cortisol, IgA), heart rate, and self-reports. Participants will fill out a daily diary each morning starting the day after session 1 until the day of session 5 with their self-reports.
Change in incidence of adverse events of cannabinoids across conditions
Assessed through self-reports from study participants (semi-structured interviews) and clinically significant adverse changes in vital signs (heart rate, blood pressure).
Procedure feasibility
Measured via means and rates of study recruitment
Protocol feasibility
Measured via means and rates of study recruitment

Secondary Outcome Measures

Change in performance on behavioral impulsivity tasks across conditions
Measured by Delay and Probability Discounting Procedure, Experiential Discounting Task, and the Hybrid Response Inhibition Task
Change in sleep quality across conditions
Measured via wrist-worn actigraphy using the Fatigue Science Readiband and self-report based on the Pittsburgh Sleep Inventory
Change in subjective response to cannabis
Measured via Drug Effects Questionnaire, assessing aspects of subjective response on a scale from "Not at All" to "Extremely", "Dislike Very Much" to "Like Very Much", and other variations.
Change in state anxiety across conditions
Measured by State Anxiety sub-scale of the State Trait Anxiety sub-scale, rating experience from "Not at All" to "Very Much"
Change in psychological distress across conditions
Measured by the standardized Short Form of the Profile of Mood States, assessing experience of various feelings from "Not at All" to "Extremely"

Full Information

First Posted
January 25, 2022
Last Updated
October 20, 2023
Sponsor
University of British Columbia
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1. Study Identification

Unique Protocol Identification Number
NCT05261321
Brief Title
Cannabis and Polysubstance Use: Response Inhibition and Stress Exposure
Acronym
CAPU RISE
Official Title
Cannabis and Polysubstance Use: Response Inhibition and Stress Exposure
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 15, 2022 (Actual)
Primary Completion Date
December 2024 (Anticipated)
Study Completion Date
December 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of British Columbia

4. Oversight

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

5. Study Description

Brief Summary
The purpose of this Phase I non-therapeutic trial is to examine the neurological effects of cannabis on stress reactivity and inhibition in healthy cannabis users. We expect differences between high ratio CBD:THC cannabis oil, low ratio CBD:THC cannabis oil, and/or placebo on outcome measures.
Detailed Description
Purpose: To examine the neurological effects of cannabis on stress reactivity and inhibition in healthy adults using recreational cannabis. This is a phase I/pilot healthy subjects trial. Primary Hypotheses: The intervention will be feasible to implement Cannabis oil will attenuate stress, measured via biological and self-report data, including salivary molecules, functional Magnetic Resonance Imaging, and standardized psychosocial assessments. Justification: Current cannabis research focuses on medical uses for cannabis, clinical populations and/or non-commercially available products. There remains limited experimental research on the effects of commercial products in non-clinical regular users of cannabis. Further, most drug use research excludes polysubstance users. Given the high number of people using cannabis to cope with stress, biological evidence is needed to determine the validity of this claim. Stress is known to negatively impact daily functioning and has been linked to poorer mental and physical health outcomes. The effects of cannabinoids on cognitive functioning also have implications for daily functioning. Objectives: Determine a causal link between commercially available cannabinoid products and mechanisms involved with stress response in polysubstance users, specifically weekly cannabis users with heavy drinking (males: minimum 5 drinks, females: minimum 4 drinks on at least one occasional per month for the past 12 months). Examine the short-term effects of cannabinoids on sleep quality in this population. Study Design: The study is a Phase I non-therapeutic pilot trial and will utilize a double-blind, placebo-controlled, within-subjects design. The acute effects of the investigational products (IPs) will be examined. Each participant will undergo an initial phone screen and 5 sessions, with sessions 2-4 involving drug administration. There will be three investigational product arms for the drug administration sessions: cannabis oil with a high ratio of THC to CBD, cannabis oil with a high ratio of CBD to THC, and placebo. Each participant will be exposed to all three arms, one per drug administration session. The order of arm will be randomized. Each drug administration session will be a minimum of10 days apart to ensure a sufficient washout period.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Healthy
Keywords
cannabis, cannabinoids, stress, neuroimaging, fMRI

7. Study Design

Primary Purpose
Basic Science
Study Phase
Phase 1
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigator
Masking Description
Double-blinded masking.
Allocation
Randomized
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Cannabis oil with a high ratio of THC to CBD
Arm Type
Active Comparator
Arm Description
Participants will be given a single dose of oral cannabis oil containing 5mg THC and 0.17mg CBD.
Arm Title
Cannabis oil with a high ratio of CBD to THC
Arm Type
Active Comparator
Arm Description
Participants will be given a single dose of oral cannabis oil containing 5mg THC and 25mg CBD.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Participants will be given a single dose of 1 mL placebo (carrier oil with botanical terpenes) via oral route of administration.
Intervention Type
Drug
Intervention Name(s)
Cannabis oil with a high ratio of THC to CBD
Intervention Description
In the first active condition, cannabis oil with a high THC to CBD ratio will be administered to participants.
Intervention Type
Drug
Intervention Name(s)
Cannabis oil with a high ratio of CBD to THC
Intervention Description
In the second active condition, cannabis oil with a high CBD to THC ratio will be administered to participants.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
In the control condition, the placebo will be administered to participants.
Primary Outcome Measure Information:
Title
Change in stress response across conditions
Description
Indicated by differences in blood-oxygenation-level-imaging (BOLD) response via functional magnetic resonance imaging (fMRI), salivary stress molecule levels (eg cortisol, IgA), heart rate, and self-reports. Participants will fill out a daily diary each morning starting the day after session 1 until the day of session 5 with their self-reports.
Time Frame
5 weeks
Title
Change in incidence of adverse events of cannabinoids across conditions
Description
Assessed through self-reports from study participants (semi-structured interviews) and clinically significant adverse changes in vital signs (heart rate, blood pressure).
Time Frame
5 weeks
Title
Procedure feasibility
Description
Measured via means and rates of study recruitment
Time Frame
Through study completion; average of 1 year
Title
Protocol feasibility
Description
Measured via means and rates of study recruitment
Time Frame
Through study completion; average of 1 year
Secondary Outcome Measure Information:
Title
Change in performance on behavioral impulsivity tasks across conditions
Description
Measured by Delay and Probability Discounting Procedure, Experiential Discounting Task, and the Hybrid Response Inhibition Task
Time Frame
5 weeks
Title
Change in sleep quality across conditions
Description
Measured via wrist-worn actigraphy using the Fatigue Science Readiband and self-report based on the Pittsburgh Sleep Inventory
Time Frame
5 weeks
Title
Change in subjective response to cannabis
Description
Measured via Drug Effects Questionnaire, assessing aspects of subjective response on a scale from "Not at All" to "Extremely", "Dislike Very Much" to "Like Very Much", and other variations.
Time Frame
5 weeks
Title
Change in state anxiety across conditions
Description
Measured by State Anxiety sub-scale of the State Trait Anxiety sub-scale, rating experience from "Not at All" to "Very Much"
Time Frame
5 weeks
Title
Change in psychological distress across conditions
Description
Measured by the standardized Short Form of the Profile of Mood States, assessing experience of various feelings from "Not at All" to "Extremely"
Time Frame
5 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion criteria: Are 19-35 years old at the start of the study Have used oral cannabis for non-medical purposes twice the past month (30 days) Have previously used a minimum of 20mg of CBD Have previously used a minimum of 5mg THC 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. Females: are not undergoing alternative fertility methods, such as IVF, or otherwise trying to start a family for the duration of participation Males: will not be donating sperm at some point during the duration of participation Are able to provide informed consent Are able to complete assessments in English Are able to attend sessions according to the study schedule Will provide proof of 2 doses of an approved COVID-19 vaccination Exclusion criteria: Are left-handed or ambidextrous Females: are pregnant, nursing, or not on safe pregnancy protection Are trying to conceive Have a known or suspected allergy to cannabinoids and/or palm/coconut oil 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 Have had an adverse reaction (unwanted, unexpected reaction or symptoms) to cannabis within last 6 months Have a major physical problem/health concern, including: Liver-cirrhosis or other liver disease Diabetes Chronic illness that may increase risk for adverse reactions to cannabis Chronic pain Genetic glucuronidation disorders (e.g., Gilbert's disease) 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 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) Are taking any of the following medications: Any medication that impacts the central nervous system, brain, and/or metabolic system Psychotropic medications, sedatives, and central nervous system depressants, including sleeping pills, tranquilizers, some pain medications, some allergy and cold medications, and anti-seizure medications Medications otherwise affecting the central nervous system, including amphetamines and other sympathomimetics Allergy medications (antihistamines; within 24 hours) Heart medications Blood pressure medication Steroid medications Opioids or other pain medications Anticholinergics: drugs that block acetylcholine, a chemical signal that plays a role in memory and learning. Drugs metabolized by cytochrome P450 enzymes, including amitriptyline, fentanyl, sufentanil, and alfentanil Highly protein-bound drugs, including warfarin, cyclosporine, and amphtericin Drugs metabolized by UGT enzymes, including propofol, antivirals Antiretroviral drugs Stomach acid inhibitors Antibiotics and antifungal medications Heart medications 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) 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. Work nightshifts Have any diagnosed sleep disorders Have dyscalculia Have a neurodevelopmental disorder or cognitive impairments, including: Autism Spectrum Disorder Attention Deficit/Hyperactivity Disorder (ADHD) Have schizophrenia spectrum disorder and/or history of psychosis 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 Any diagnosed current mental health disorder and/or diagnosis of a mental health disorder within the past year 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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Christian G Schütz, MD PhD
Phone
778-873-4785
Email
christian.schutz@ubc.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Karina A Thiessen, BA BEd
Phone
6042400051
Email
karina.thiessen@ubc.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christian G Schütz, MD PhD
Organizational Affiliation
University of British Columbia; British Columbia Mental Health and Substance Use Services
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Karina A Thiessen, BA BEd
Organizational Affiliation
University of British Columbia
Official's Role
Study Director
Facility Information:
Facility Name
B.R.A.I.N. Lab, Institute of Mental Health, Faculty of Medicine, University of British Columbia
City
Vancouver
State/Province
British Columbia
ZIP/Postal Code
V6T 1Z3
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Christian G Schütz, MD PhD
Phone
778-873-4785
Email
christian.schutz@ubc.ca
First Name & Middle Initial & Last Name & Degree
Karina A Thiessen, BA BEd
Phone
6042400051
Email
karina.thiessen@ubc.ca

12. IPD Sharing Statement

Plan to Share IPD
No

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Cannabis and Polysubstance Use: Response Inhibition and Stress Exposure

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