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NCT Number: NCT04935619

Extended Effects of Cannabis Abstinence on Clinical Symptoms and Cognition in Depression

The prevalence of major depressive disorder (MDD) is ~5.0%, and rates of co-occurring SUDs in these patients approach 40-50%. Specifically, rates of co-morbid cannabis use disorder (CUD) in patients with MDD are elevated 2-3 fold compared to 2.9% in the general population, and is associated with poorer treatment outcomes and impaired cognitive and psychosocial functioning in comparison to MDD patients without CUD. Most studies of cannabis use in MDD are cross-sectional in design, and therefore causal relationships are unclear. This study investigates the effects of cannabis abstinence over a 28-day period in patients with MDD with co-occurring CUD using a randomized controlled design, namely contingent reinforcement.

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Key information

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Centre for Addiction and Mental Health

Toronto, Ontario, M5T 1R8, Canada

Location status: Recruiting

Location contact

Tony P George, M.D.

PRINCIPAL_INVESTIGATOR

About this study

The prevalence of major depressive disorder (MDD) is ~5.0%, and rates of co-occurring SUDs in these patients approach 40-50%. Specifically, rates of co-morbid cannabis use disorder (CUD) in patients with MDD are elevated 2-3 fold compared to 2.9% in the general population, and is associated with poorer treatment outcomes and impaired cognitive and psychosocial functioning in comparison to MDD patients without CUD. To date, most studies of cannabis use in MDD were cross-sectional in design, and therefore causal relationships are unclear. The investigators previous studies in cannabis dependent patients with schizophrenia suggest that extended cannabis abstinence (up to 28 days) using contingent reinforcement is associated with improvements in specific areas of cognition (e.g. verbal learning and memory) and depressive symptoms. A more recent study using an open-label design demonstrated that 28 days of cannabis abstinence improves depressive symptoms and anhedonia in participants (N=11) with co-occurring MDD and CUD.

The investigators propose a controlled cannabis abstinence paradigm in patients with co-morbid MDD and CUD (N=52) to further investigate these findings. Stabilized MDD patients with moderate to severe CUD will be randomly assigned to one of two groups: 1) A contingent reinforcement (CR) intervention (n=26); 2) a non-contingent reinforcement (NCR) intervention (n=26), which will serve as a time and non-abstinence control. In the CR group, subjects achieving biochemically-verified cannabis abstinence at study endpoint (Day 28) will receive a $300 contingent payment; participants in the NCR group will not receive this contingent payment. The primary outcomes are: 1) cannabis abstinence rates at Day 28 in CR versus NCR groups; 2) changes in mood (depressive), anxiety and sleep symptoms over the 28-day assessment period. Secondary outcomes include cognition.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • All participants must be between the ages 18-55
  • Meet SCID for DSM-5 diagnostic criteria for cannabis use disorder, moderate to severe
  • Meet SCID for DSM-5 diagnostic criteria for Major Depressive Disorder
  • Be an outpatient receiving a stable dose of antidepressant medication for at least three months (to ensure stability of depressive symptoms
  • Have a Hamilton Depression Rating Scale (HDRS-17) at baseline assessment in the range of 12-25..
  • Have a Full-Scale IQ ≥ 80 as determined by the WTAR
  • Be a non-treatment seeking cannabis user
  • Evidence of sufficient motivation and effort as measured by a Test of Memory Malingering (TOMM) score ≥ 45.

Exclusion criteria

  • Meets criteria for substance use disorder of alcohol or other illicit substances within the past 6 months (with the exception of cannabis, nicotine, or caffeine)
  • Positive urine screen for illicit substances other than cannabis, nicotine, or caffeine
  • Current suicidal or homicidal ideation
  • Psychotic disorder diagnosis (e.g. schizoaffective disorder, major depression with psychotic features) as determined by the SCID
  • Treatment seeking for cannabis use
  • Meet SCID for DSM-5 diagnostic criteria for Bipolar Disorder
  • Head Injury> 5 minutes LOC
  • Exceed upper and lower cut-offs on HSRD-17 (See Inclusion Criteria)

Treatment and study plan

Contingency Reinforcement

Behavioral

Subjects will be randomly assigned on a 1:1 ratio to either the Contingency Reinforcement or Non-Contingency Reinforcement Intervention prior to their in-person screening visit.

Non-Contingency Reinforcement

Behavioral

Subjects will be randomly assigned on a 1:1 ratio to either the Contingency Reinforcement or Non-Contingency Reinforcement Intervention prior to their in-person screening visit.

Primary outcomes

  1. Changes in Depressive Symptomology from Baseline to Week 4

    Time frame: [Time Frame: Weekly (Day 0, Day 7, Day 14, Day 21, Day 28)]

    The Hamilton Depression Rating Scale will be administered to assess severity of depressive symptoms. [Min score = 0, Max score = 52; Higher scores evince more severe symptomology]

  2. Changes in Anxious Symptomology from Baseline to Week 4

    Time frame: [Time Frame: Weekly (Day 0, Day 7, Day 14, Day 21, Day 28)]

    The Beck Anxiety Inventory will be administered to assess severity of anxiety symptoms [Min score = 0, Max score = 63; Higher scores evince more severe symptomology].

  3. Changes in Sleep Symptomology from Baseline to Week 4

    Time frame: [Time Frame: Weekly (Day 0, Day 7, Day 14, Day 21, Day 28)]

    The Pittsburgh Sleep Quality Index will be administered weekly to examine quality of sleep and other sleep disturbances [Min score = 0, Max score = 21; Higher scores evince more severe symptomology].

  4. Changes in Anhedonia from Baseline to Week 4

    Time frame: [Time Frame: Weekly (Day 0, Day 7, Day 14, Day 21, Day 28)]

    The Snaith-Hamilton Pleasure Scale will be administered weekly to measure changes in anhedonia [Min score = 0, Max score = 14; Higher scores evince more severe symptomology].

Secondary outcomes

  1. Changes in Verbal Learning and Memory

    Time frame: Day 0 and Day 28

    The Hopkins Verbal Learning Test will be administered to investigate this cognitive domain.

  2. Changes in Attention and Visual Search

    Time frame: Day 0 and Day 28

    The Trail Making Test will be administered to investigate these cognitive domains

  3. Changes in Working Memory

    Time frame: Day 0 and Day 28

    The Digit Span test will be administered to investigate this cognitive domain.

  4. Changes in Sustained Attention

    Time frame: Day 0 and Day 28

    The Continuous Performance Test will be administered to investigate this cognitive domain

Study contacts

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

Maryam Sorkhou, HBSc

CONTACT

[email protected]

4165358501 ext. 36225

Sponsors and collaborators

Lead sponsor

Centre for Addiction and Mental Health

Other

Registry information

Official study title

Effects of Extended Cannabis Abstinence on Clinical and Cognitive Outcomes in Patients With Co-Morbid Major Depressive and Cannabis Use Disorders

Important dates

Study start
2021
Primary completion
2027
Study completion
2027
First posted
Jun 23, 2021
Registry last updated
Feb 24, 2025

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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