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…
Conditions studied
Cannabis Use, Major Depressive Disorder, Cognitive Impairment
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. 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.
Interventions
- Behavioral: Contingency Reinforcement — 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.
- Behavioral: Non-Contingency Reinforcement — 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
- Changes in Depressive Symptomology from Baseline to Week 4 ([Time Frame: Weekly (Day 0, Day 7, Day 14, Day 21, Day 28)])
- Changes in Anxious Symptomology from Baseline to Week 4 ([Time Frame: Weekly (Day 0, Day 7, Day 14, Day 21, Day 28)])
- Changes in Sleep Symptomology from Baseline to Week 4 ([Time Frame: Weekly (Day 0, Day 7, Day 14, Day 21, Day 28)])
- Changes in Anhedonia from Baseline to Week 4 ([Time Frame: Weekly (Day 0, Day 7, Day 14, Day 21, Day 28)])
Eligibility information
Study locations
- Centre for Addiction and Mental Health, Toronto, Ontario M5T 1R8 Canada
Source: ClinicalTrials.gov. Record last refreshed by Varda Clinical: 2026-09-27.