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NCT Number: NCT05445180

Investigating the Neural Correlates of Cognitive Function in Psychosis Patients and Non-Psychiatric Controls With Cannabis Use

Cognitive impairment is well established in people with psychosis and is associated with cannabis use. The current study will investigate the neurobiological basis of cognitive change associated with 28-days of cannabis abstinence in people with psychosis and non-psychiatric controls with cannabis use. Participants will be randomized to a cannabis abstinent group or a non-abstinent control group and will undergo magnetic resonance imaging at baseline and following 28-days of abstinence. This study will help characterize the neuropathophysiological processes underlying cognitive dysfunction associated with cannabis use and its recovery which may guide the development of novel interventions for problematic cannabis use.

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Key information

Age range

16 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Douglas Mental Health University Institute

Montreal, Quebec, H4H 1R3, Canada

Location status: Recruiting

Location contact

Rachel Rabin, Ph. D.

PRINCIPAL_INVESTIGATOR

Research Coordinator

CONTACT

[email protected]

(514) 761-6131 ext. 3348

About this study

Background/Importance: Cognitive impairment is well established in people with psychosis and is associated with cannabis use. Despite high rates of cannabis use among people with psychosis and the general population, cannabis' effects on cognition and the brain and their recovery remain unclear. Therefore, this study will investigate the neurobiological basis of changes in cognitive processes associated with cannabis abstinence in people with psychosis and non-psychiatric controls.

Aims: To examine the effects of 28-days of cannabis abstinence in psychosis patients with cannabis use and non-psychiatric controls with cannabis use on (i) brain activity (paired with a memory task); (ii) brain morphology; (iii) to determine if changes in memory following 28-days of abstinence correlate with changes in brain activity and/or morphology and (iv) to determine if baseline brain function and morphology can predict successful abstinence.

Methods: Seventy-four psychosis patients with cannabis use and 60 non-psychiatric controls with cannabis use will be randomized to: (1) contingency reinforcement where biochemically verified abstinence at day 28 will be rewarded; or (2) a non-abstinent control group. The investigators will also recruit a group of healthy non-psychiatric controls (n=40) to determine if neural outcomes in cannabis-using participants do indeed normalize ("recover") following abstinence. Participants will undergo structural and functional magnetic resonance imaging while completing a memory task at baseline (pre-abstinence) and following 28-days of abstinence. Urine samples will be collected twice weekly for abstinence verification.

Relevance: This study will help to characterize the neuropathophysiological processes underlying cognitive dysfunction associated with cannabis use in people with psychosis and non-psychiatric controls which may help to guide the development of novel neurobiologically-informed interventions to treat problematic cannabis use.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Able to provide informed consent in English or French
  • Heavy cannabis use (defined as weekly cannabis use for at six months) and/or DSM-5 diagnosis of CUD
  • Have a Full-Scale IQ ≥ 75
  • Meet DSM-5 criteria for a psychotic disorder (psychosis patient arm only)
  • Be an outpatient receiving a stable dose of medication(s) for at least two months (psychosis patient arm only)
  • Clinically stable (as measured by the PANSS-6, total score <30) (psychosis patient arm only)

Exclusion criteria

  • current SUD (other than CUD)
  • MRI contraindications
  • Positive urine screen for psychoactive substances other than cannabis, nicotine, or caffeine
  • Current suicidal or homicidal ideation
  • Head injury requiring hospitalization or loss of consciousness > 5 minutes
  • Current medical diseases that requires hospitalization or regular monitoring
  • Being pregnant
  • DSM-5 Axis 1 diagnosis (other than CUD) (non-psychiatric controls only)
  • Taking psychotropic medication

Treatment and study plan

Contingency Management

Behavioral

Contingency management will be used to encourage abstinence

Primary outcomes

  1. Change in fMRI brain activity pattern

    Time frame: Baseline, Day 28

    fMRI will be used to measure differences between baseline (day 0) and day 28 in hemodynamic (BOLD) responses while participants complete a memory task

  2. Change in behavior during fMRI task

    Time frame: Baseline, Day 28

    Behavioral responses (episodic memory performance) will be recorded by an external button box. These responses will be used to assess encoding accuracy during an episodic memory task.

Secondary outcomes

  1. Change in brain morphology: gray matter volume

    Time frame: Baseline, Day 28

    Using MRI, changes in gray matter volume will be analyzed from baseline (day 0) to day 28

  2. Change in brain morphology: cortical thickness

    Time frame: Baseline, Day 28

    Using MRI, changes in cortical thickness will be analyzed from baseline (day 0) to day 28

  3. Change in brain morphology: diffusion

    Time frame: Baseline, Day 28

    Using MRI, changes in diffusion based measures will be analyzed from baseline (day 0) to day 28

Study contacts

Contact information is provided by the study sponsor or research team.

Charlene Osei-Afrifa

CONTACT

[email protected]

(514) 761-6131 ext. 3348

Sponsors and collaborators

Lead sponsor

Douglas Mental Health University Institute

Other

Registry information

Official study title

Investigating the Neural Correlates of Cognitive Function Associated With Cannabis Abstinence in Psychosis Patients and Non-Psychiatric Controls With Cannabis Use

Important dates

Study start
2022
Primary completion
2027
Study completion
2027
First posted
Jul 6, 2022
Registry last updated
May 22, 2026

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.

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