search
Back to results

Marijuana Cue-Reactivity & Seeking Behavior in Regular Cannabis Users (MCN)

Primary Purpose

Marijuana Abuse

Status
Active
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
N-acetyl cysteine
Sponsored by
Wayne State University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Marijuana Abuse

Eligibility Criteria

21 Years - 55 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Participants will be healthy individuals 21-55 year olds who use marijuana.
  • Marijuana use will be verified by self-report and THC-positive urine samples. -Participants must meet DSM 5 criteria for Cannabis Use Disorder and be willing to participate in research but not seeking treatment.

Exclusion Criteria:

  • Candidates with the following conditions will be excluded:
  • Serious psychiatric illness (e.g. psychotic or bipolar disorder
  • Recent (past 5 years) suicide attempts
  • Major depression that is not substance-induced)
  • Substance Use Disorders (SUD) other than Cannabis or Nicotine Use Disorders and Mild Alcohol Use Disorder
  • Neurological diseases (e.g. stroke, seizures)
  • Cardiovascular problems (e.g. myocardial infarction, angina, systolic BP >160 or <95 mmHg, diastolic BP >95 mmHg, clinically abnormal ECG)
  • Pulmonary diseases (e.g. asthma, TB)
  • Systemic diseases (e.g. hepatitis, autoimmune, Cushing syndrome)
  • Cognitive impairment (<80 IQ)
  • Past-month exposure to medications that increase study risk (e.g. toxicity to major organs, asthma inhalers)
  • Women who are pregnant (urine HCG), lactating (self-report), or if heterosexually active and not using (self-report) medically approved birth control measures (oral/depot contraceptives, IUD, condom/foam, sterilization, tubal ligation)
  • Seeking treatment for a Substance Use Disorder.
  • Individuals unable to give voluntary informed consent will be excluded. Applicants interested in treatment will be excluded from the study and referred to a treatment program.

Sites / Locations

  • Tolan Park Medical Building

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Placebo Comparator

Placebo Comparator

Active Comparator

Active Comparator

Arm Label

N-acetylcysteine 0mg X Cue Exposure (neutral)

N-acetylcysteine 0mg X Cue Exposure (marijuana)

N-acetylcysteine 2400mg X Cue Exposure (neutral)

N-acetylcysteine 2400mg X Cue Exposure (marijuana)

Arm Description

Outcomes

Primary Outcome Measures

Marijuana Craving Visual Analog Scale (VAS) (Self-report measure)
Marijuana Craving Questionnaire (Self-report measure)
Marijuana Rating Form (Self-report measure)
Subjective Effects Scale Visual Analog Scale (VAS) (Self-report measure)
Questionnaire of Smoking Urges (Self-report measure)
Marijuana Withdrawal Checklist
NAC Side Effect Checklist
Systolic blood pressure (physiological effects)
Diastolic blood pressure (physiological effects)
Heart rate (physiological effects)
Core-body temperature (physiological effects)

Secondary Outcome Measures

Full Information

First Posted
April 25, 2017
Last Updated
February 23, 2022
Sponsor
Wayne State University
search

1. Study Identification

Unique Protocol Identification Number
NCT03154580
Brief Title
Marijuana Cue-Reactivity & Seeking Behavior in Regular Cannabis Users
Acronym
MCN
Official Title
Marijuana Cue-Reactivity & Seeking Behavior in Regular Cannabis Users: A Pilot Test of Glutamatergic Modulation
Study Type
Interventional

2. Study Status

Record Verification Date
February 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
May 1, 2017 (Actual)
Primary Completion Date
May 28, 2022 (Anticipated)
Study Completion Date
May 28, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Wayne State University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of the proposed study is to examine the relationship between marijuana reminders, or "cues", craving for marijuana, and marijuana use. The principal investigator is also assessing whether N-acetylcysteine, can reduce marijuana craving or use.
Detailed Description
This study involves three screening sessions that could last about 3 hours each. Part of this study will be conducted on an inpatient unit where the participant will live for 4 straight nights. During the inpatient stay participants will participant in experimental sessions where they will be asked to smoke cigarettes containing either marijuana or placebo (a blank). Participants will be asked to take capsules that could contain N-acetylcysteine or placebo (blank). Participants will be asked to complete questionnaires and have vital signs (blood pressure, heart rate) monitored. Participants will be asked to participate in overnight sleep recordings, a polysomnogram (PSG).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Marijuana Abuse

7. Study Design

Primary Purpose
Basic Science
Study Phase
Phase 1
Interventional Study Model
Crossover Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
21 (Actual)

8. Arms, Groups, and Interventions

Arm Title
N-acetylcysteine 0mg X Cue Exposure (neutral)
Arm Type
Placebo Comparator
Arm Title
N-acetylcysteine 0mg X Cue Exposure (marijuana)
Arm Type
Placebo Comparator
Arm Title
N-acetylcysteine 2400mg X Cue Exposure (neutral)
Arm Type
Active Comparator
Arm Title
N-acetylcysteine 2400mg X Cue Exposure (marijuana)
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
N-acetyl cysteine
Intervention Description
Participants will receive 4 capsules at 11:15am on each experimental session day.
Primary Outcome Measure Information:
Title
Marijuana Craving Visual Analog Scale (VAS) (Self-report measure)
Time Frame
Change is being assessed. Marijuana Craving VAS administered at baseline 0900, at 0930, 1000, 1030, 1100, 1230, 1250, 1310, 1320, 1330, 1345, 1400, 1430, 1500, 1530, and 1600.
Title
Marijuana Craving Questionnaire (Self-report measure)
Time Frame
Change is being assessed. Marijuana Craving Quest.administered at baseline 0900, at 0930, 1000, 1030, 1100, 1230, 1345, 1400, 1430, 1500, 1530, and 1600.
Title
Marijuana Rating Form (Self-report measure)
Time Frame
Change is being assessed. Marijuana Rating Form administered at baseline 0900, at 0930, 1000, 1030, 1100, 1230, 1345, 1400, 1430, 1500, 1530, and 1600.
Title
Subjective Effects Scale Visual Analog Scale (VAS) (Self-report measure)
Time Frame
Change is being assessed. Subjective Effects Scale administered at baseline 0900, at 0930, 1000, 1030, 1100, 1230, 1345, 1400, 1430, 1500, 1530, and 1600.
Title
Questionnaire of Smoking Urges (Self-report measure)
Time Frame
Change is being assessed. Questionnaire is administered at baseline 0900, at 0930, 1000, 1030, 1100, 1230, 1345, 1400, 1430, 1500, 1530, and 1600.
Title
Marijuana Withdrawal Checklist
Time Frame
Change is being assessed. Questionnaire is administered at baseline 0900, at 0930, 1000, 1030, 1100, 1230, 1345, 1400, 1430, 1500, 1530, and 1600.
Title
NAC Side Effect Checklist
Time Frame
Change is being assessed. Questionnaire is administered at baseline 0900, at 0930, 1000, 1030, 1100, 1230, 1345, 1400, 1430, 1500, 1530, and 1600.
Title
Systolic blood pressure (physiological effects)
Time Frame
Change is being assessed. Systolic blood pressure measured at baseline 0900, at 0930, 1000, 1030, 1100, 1230, 1345, 1400, 1430, 1500, 1530, and 1600.
Title
Diastolic blood pressure (physiological effects)
Time Frame
Change is being assessed. Diastolic blood pressure measured at baseline 0900, at 0930, 1000, 1030, 1100, 1230, 1345, 1400, 1430, 1500, 1530, and 1600.
Title
Heart rate (physiological effects)
Time Frame
Change is being assessed. Heart rate measured at baseline 0900, at 0930, 1000, 1030, 1100, 1230, 1345, 1400, 1430, 1500, 1530, and 1600.
Title
Core-body temperature (physiological effects)
Time Frame
Change is being assessed. Core-body temperature measured at baseline 0900, at 0930, 1000, 1030, 1100, 1230, 1345, 1400, 1430, 1500, 1530, and 1600.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Participants will be healthy individuals 21-55 year olds who use marijuana. Marijuana use will be verified by self-report and THC-positive urine samples. -Participants must meet DSM 5 criteria for Cannabis Use Disorder and be willing to participate in research but not seeking treatment. Exclusion Criteria: Candidates with the following conditions will be excluded: Serious psychiatric illness (e.g. psychotic or bipolar disorder Recent (past 5 years) suicide attempts Major depression that is not substance-induced) Substance Use Disorders (SUD) other than Cannabis or Nicotine Use Disorders and Mild Alcohol Use Disorder Neurological diseases (e.g. stroke, seizures) Cardiovascular problems (e.g. myocardial infarction, angina, systolic BP >160 or <95 mmHg, diastolic BP >95 mmHg, clinically abnormal ECG) Pulmonary diseases (e.g. asthma, TB) Systemic diseases (e.g. hepatitis, autoimmune, Cushing syndrome) Cognitive impairment (<80 IQ) Past-month exposure to medications that increase study risk (e.g. toxicity to major organs, asthma inhalers) Women who are pregnant (urine HCG), lactating (self-report), or if heterosexually active and not using (self-report) medically approved birth control measures (oral/depot contraceptives, IUD, condom/foam, sterilization, tubal ligation) Seeking treatment for a Substance Use Disorder. Individuals unable to give voluntary informed consent will be excluded. Applicants interested in treatment will be excluded from the study and referred to a treatment program.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Leslie Lundahl, PhD
Organizational Affiliation
Wane State University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Tolan Park Medical Building
City
Detroit
State/Province
Michigan
ZIP/Postal Code
48201
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Marijuana Cue-Reactivity & Seeking Behavior in Regular Cannabis Users

We'll reach out to this number within 24 hrs