Skip to main content
OpenTrials
Completed

NCT Number: NCT03154567

Effects of Stress and Drug-cue Exposure (SCM)

The purpose of the proposed study to examine the links among stress, craving for marijuana, and marijuana reminders, or "cues".

In this study, an agent called yohimbine will be used to produce stress-like responses. Yohimbine is known to cause stress response in studies of alcohol and other substance use disorders. This study intends to show it can be used to cause stress in marijuana users as well.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Marijuana Abuse Chemically-Induced Disorders Mental Disorders Substance-Related Disorders

Age range

21 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Tolan Park Medical Building

Detroit, Michigan, 48201, United States

About this study

Part of this study will be conducted on a residential unit where participants will live for 7 nights over a 2-week period (4 consecutive nights the 1st week and 3 consecutive nights the 2nd week).

During that time, participants can't leave the unit unescorted or have visitors.

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 yohimbine or placebo (blank).

Participants will be asked to complete questionnaires and will have their vital signs (blood pressure, heart rate) monitored throughout each session.

Participants will be asked to participate in overnight sleep recordings, a polysomnogram (PSG).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Participants (18-55 yr) will be current marijuana users, based on self-report and THC-positive urine samples.
  • Candidates must meet DSM-5 criteria for Mild-to-Moderate Cannabis Use Disorder (CUD) and be willing to participate in research but not seeking treatment.
  • Candidates must be in good health, as assessed using data from psychiatric evaluation, extensive substance use history interview, and medical evaluations including medical history, physical exam, standard lab tests and 12-lead ECG.

Exclusion criteria

Candidates with the following conditions will be excluded:

  • Serious psychiatric illness (e.g. psychotic or bipolar disorder, recent suicide attempts, major depression).
  • Substance Use Disorders other than Cannabis or Nicotine Use Disorders and Mild Alcohol Use Disorder.
  • Neurological diseases
  • Cardiovascular problems (e.g. including systolic BP >140 or <95 mmHg, diastolic BP >90 mmHg, abnormal ECG).
  • Pulmonary diseases
  • Systemic diseases
  • Cognitive impairment (<80 IQ)
  • Past-month medications that increase study risk.
  • Women who are pregnant, lactating, or if heterosexually active and not using medically approved birth control.
  • Candidates seeking Substance Use Disorder treatment.
  • Individuals unable to give voluntary informed consent will be excluded.

Treatment and study plan

Yohimbine

Drug

Yohimbine (0mg, 20mg, or 40 mg) will be administered at 11:00am on each of the experimental sessions.

Primary outcomes

  1. Marijuana Craving Visual Analog Scale (VAS) (Self-report measure)

    Time frame: Change is being assessed. Marijuana Craving VAS administered at baseline 0900. It will then be administered at 1000, 1030, 1100, 1200, 1220, 1245, 1300, 1315, 1345.

  2. Marijuana Craving Questionnaire (Self-report measure)

    Time frame: Change is being assessed. Marijuana Craving Quest.administered at baseline 0900. It will then be administered at 1000, 1030, 1100, 1200, 1410, 1430, 1500, 1530, 1600, 1630.

  3. Questionnaire of Smoking Urges (Self-report measure)

    Time frame: Change is being assessed. Questionnaire is administered at baseline 0900. It will then be administered at 1000, 1030, 1100, 1200, 1410, 1430, 1500, 1530, 1600, 1630.

  4. Marijuana Rating Form (Self-report measure)

    Time frame: Change is being assessed. Marijuana Rating Form is administered 30 minutes after each smoking episode in the sampling session.

  5. Marijuana Withdrawal Checklist

    Time frame: Change is being assessed. Questionnaire is administered every morning and evening.

  6. Subjective Effects Scale Visual Analog Scale (VAS) (Self-report measure)

    Time frame: Change is being assessed. Subjective Effects Scale administered at baseline 0900.It will then be administered at 1000, 1030, 1100, 1200, 1410, 1430, 1500, 1530, 1600, 1630.

  7. Positive & Negative Affect Schedule (Self-report measure)

    Time frame: Change is being assessed. Questionnaire is administered at baseline 0900. It will then be administered at 1000, 1030, 1100, 1200, 1410, 1430, 1500, 1530, 1600, 1630.

  8. Systolic blood pressure (physiological effects)

    Time frame: Change is being assessed. Systolic blood pressure measured at baseline 0900. It will then be measure at 1000, 1030, 1100, 1200, 1410, 1430, 1500, 1530, 1600, 1630.

  9. Diastolic blood pressure (physiological effects)

    Time frame: Change is being assessed. Diastolic blood pressure measured at baseline 0900. It will then be measure at 1000, 1030, 1100, 1200, 1410, 1430, 1500, 1530, 1600, 1630.

  10. Heart rate (physiological effects)

    Time frame: Change is being assessed. Heart rate measured at baseline 0900. It will then be measure at 1000, 1030, 1100, 1200, 1410, 1430, 1500, 1530, 1600, 1630.

  11. Core-body temperature (physiological effects)

    Time frame: Change is being assessed. Core-body temperature measured at baseline 0900. It will then be measure at 1000, 1030, 1100, 1200, 1410, 1430, 1500, 1530, 1600, 1630.

Sponsors and collaborators

Lead sponsor

Wayne State University

Other

Registry information

Official study title

Effects of Stress and Drug-cue Exposure on Craving and Marijuana Seeking Behavior in Regular Cannabis Smokers

Important dates

Study start
2017
Primary completion
2023
Study completion
2023
First posted
May 16, 2017
Registry last updated
Apr 23, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Related clinical trials

Published trials that share one or more normalized conditions with this study.