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| Name | Class |
|---|---|
| Sheppard Pratt Health System | OTHER |
| University of California, Los Angeles | OTHER |
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A large proportion of people with a schizophrenia-spectrum disorder, especially in the early stages of the disease, regularly consume cannabis. Cannabis use is associated with poor prognostic outcome; however, there are no effective interventions targeted at reducing cannabis use or its deleterious effects in this population. The present trial is designed to test whether cannabidiol (CBD), a cannabinoid whose effects are in many ways antagonistic to those of Δ9-tetrahydrocannabinol (THC), can reduce psychiatric symptoms, cognitive deficits, and cannabis use in people with recent-onset psychosis who regularly consume cannabis.
This is a double-blind, randomized, placebo-controlled trial, evaluating the effects of a 12-week treatment course with CBD on psychiatric symptoms, cognition, and cannabis consumption in regular cannabis users with recent-onset psychosis. The study will be conducted at the Maryland Psychiatric Research Center (University of Maryland School of Medicine) and associated Early Intervention Programs in Baltimore, at the Sheppard Pratt Health System in Baltimore, and at the Psychosis Clinic of the University of California Los Angeles.
The daily dose of CBD is 600 mg (p.o.), administered as adjunct medication. Any non-exclusionary antipsychotic, antidepressant, anxiolytic, or other medication prescribed prior to the trial will be continued. Participants may, but do not have to be taking conventional antipsychotic medication.
The study will include 84 regular cannabis users with a schizophrenia-spectrum disorder who experienced their first psychotic episode within the last 5 years (90). Participants will be randomized 1:1 to either the CBD or the placebo group.
Outcome measures include psychiatric symptoms, cognition, global functioning, and drug use, and will be assessed at baseline, and every 3 or 6 weeks thereafter (depending on the measure), until the end of treatment at 12 weeks. Outcome will be assessed again at a 3-month follow-up.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Cannabidiol (CBD) | Experimental | Participants receive CBD daily for 12 weeks. |
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| Placebo | Placebo Comparator | Participants receive vehicle not containing any drug daily for 12 weeks. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Cannabidiol (CBD) | Drug | Participants receive a single dose of CBD (600 mg p.o.) per day for 12 weeks. |
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| Measure | Description | Time Frame |
|---|---|---|
| Change in Brief Psychiatric Rating Scale (BPRS) total score | The BPRS consists of 18 items assessing a broad range of psychiatric symptoms, including positive, negative, and affective symptoms. Each item is scored 1-7. Total scores are the sum of all items and range from 18 to 126, with larger values reflecting worse symptoms. The BPRS total score has been used widely in clinical studies of psychosis and has demonstrated reliability in assessing psychopathology across diverse psychosis populations. | Baseline and 12 weeks |
| Change in MATRICS Consensus Cognitive Battery (MCCB) composite score | The MCCB is an FDA-approved assessment tool for trials of cognition-enhancing treatments in people with schizophrenia. The MCCB is comprised of the following domains: 1) Speed of Processing; 2) Attention/Vigilance; 3) Working Memory; 4) Verbal Learning; 5) Visual Learning; 6) Reasoning and Problem Solving; and 7) Social Cognition. The composite score is standardized to a T-scale (mean=50, standard deviation=10) based on healthy control normative data. Higher scores reflect better performance. | Baseline and 12 weeks |
| Change in Serum concentrations of THCCOOH | THCCOOH is a THC metabolite and is used to quantify cannabis consumption. It has a long half-life (5-6 days) and thus provides a summary index of cannabis use within the last 1-2 weeks. | Baseline and 12 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Change in BPRS positive symptoms | The average of four BPRS key positive symptom items (conceptual disorganization, suspiciousness, unusual thought content, and hallucinatory behavior) will be analyzed as an index of antipsychotic effects of CBD. Possible values range from 1 to 7, with larger values reflecting more severe positive symptoms. | Baseline and 12 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Change in Negative Symptom Assessment (NSA-16) - exploratory | The 16-item Negative Symptom Assessment (NSA-16) is a validated and widely used scale capturing different facets of negative symptoms. Each item is scored on a scale of 1 to 6, and the total score is derived by adding individual item scores. Larger values represent worse symptoms. | Baseline and 12 weeks |
Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Semel Institute for Neuroscience and Human Behavior | Los Angeles | California | 90095 | United States | ||
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Participants will be randomized 1:1 to either the cannabidiol group or the placebo group.
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A matched placebo is employed. Only the biostatistician performing the randomization and the pharmacists will know the treatment assignment.
| Placebo | Drug | Participants receive a single daily dose of the oil vehicle used to dissolve CBD but without any active ingredient, in the same amount as the CBD group, for 12 weeks. |
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| Change in BPRS "Anxiety/Depression" subscale | This subscale will be analyzed separately to obtain an index of the anxiolytic effects of CBD. Possible values range from 1 to 7, with larger values reflecting more anxiety/depression. | Baseline and 12 weeks |
| Change in State-Trait Anxiety Inventory (STAI) - State version | The STAI-State provides another probe for potential anxiolytic effects of CBD. The participant rates 20 items about how they feel right now and a scale from 1 (not at all) to 4 (very much so). The total score is derived by adding all values and ranges from 20 to 80, with larger values indicating greater anxiety. | Baseline and 12 weeks |
| Change in MCCB Processing Speed subscale | The score is standardized to a T-scale (mean=50, standard deviation=10) based on healthy control normative data. Higher scores reflect better performance. | Baseline and 12 weeks |
| Change in MCCB Attention/Vigilance subscale | The score is standardized to a T-scale (mean=50, standard deviation=10) based on healthy control normative data. Higher scores reflect better performance. | Baseline and 12 weeks |
| Change in MCCB Working Memory subscale | The score is standardized to a T-scale (mean=50, standard deviation=10) based on healthy control normative data. Higher scores reflect better performance. | Baseline and 12 weeks |
| Change in MCCB Verbal Learning subscale | The score is standardized to a T-scale (mean=50, standard deviation=10) based on healthy control normative data. Higher scores reflect better performance. | Baseline and 12 weeks |
| Change in MCCB Visual Learning subscale | The score is standardized to a T-scale (mean=50, standard deviation=10) based on healthy control normative data. Higher scores reflect better performance. | Baseline and 12 weeks |
| Change in MCCB Reasoning/Problem solving subscale | The score is standardized to a T-scale (mean=50, standard deviation=10) based on healthy control normative data. Higher scores reflect better performance. | Baseline and 12 weeks |
| Change in MCCB Social Cognition subscale | The score is standardized to a T-scale (mean=50, standard deviation=10) based on healthy control normative data. Higher scores reflect better performance. | Baseline and 12 weeks |
| Change in The UCSD Performance-Based Skills Assessment (UPSA) | Measures ability to perform real-life tasks by standardized role-play. Scores reflect percent correct, i.e. range from 0-100, with larger scores reflecting better performance. | Baseline and 12 weeks |
| Change in Serum concentrations of THC | Index of recent cannabis use. | Baseline and 12 weeks |
| Change in Self-reported days of cannabis use | The reference period is the last three weeks. Thus, possible values range from 0 to 21. | Baseline and 12 weeks |
| Change in Cannabis Use Disorders Identification Test-Revised (CUDIT-R) | The CUDIT-R is an 8-item questionnaire probing cannabis use frequency, amount, loss of control, and adverse consequences in the last 6 months. Each item is rated on a scale from 0 to 4. The total score is derived by summing all answers and ranges from 0 to 32, with larger values representing greater use severity. | Baseline and 12 weeks |
| Change in Specific Levels of Functioning scale (SLOF) | An index of real-world, everyday functioning, derived by summing 30 item scores (1-5). Higher scores reflect better functioning. | Baseline and 12 weeks |
| Change in Behavior And Symptom Identification Scale (BASIS) - revised | A self-report questionnaire to assess mental health treatment outcomes. Only the first 24 items (probing daily life functioning, social behavior, and mood) are included, each scored on a scale from 0 to 4. The total score is derived by summing individual item scores are re-poling some items, with larger values representing worse outcome. | Baseline and 12 weeks |
| Change in Serum concentrations of CBD | To confirm bioavailability of the study drug. | Baseline and 12 weeks |
| Change in Serum concentrations of anandamide | Anandamide is an endocannabinoid that has been reported to be down-regulated by cannabis use and up-regulated by CBD. | Baseline and 12 weeks |
| Sheppard Pratt Health System |
| Baltimore |
| Maryland |
| 21204 |
| United States |
| Maryland Psychiatric Research Center | Catonsville | Maryland | 21228 | United States |
| ID | Term |
|---|---|
| D012559 | Schizophrenia |
| D002189 | Marijuana Abuse |
| D011618 | Psychotic Disorders |
| ID | Term |
|---|---|
| D019967 | Schizophrenia Spectrum and Other Psychotic Disorders |
| D001523 | Mental Disorders |
| D019966 | Substance-Related Disorders |
| D064419 | Chemically-Induced Disorders |
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| ID | Term |
|---|---|
| D002185 | Cannabidiol |
| ID | Term |
|---|---|
| D002186 | Cannabinoids |
| D013729 | Terpenes |
| D006838 | Hydrocarbons |
| D009930 | Organic Chemicals |
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