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Effects of Cannabis on Cognition and Endocannabinoid Levels in Bipolar Disorder Patients and Healthy Volunteers

Primary Purpose

Bipolar Disorder

Status
Recruiting
Phase
Early Phase 1
Locations
United States
Study Type
Interventional
Intervention
Dronabinol
Epidiolex
Placebos
Sponsored by
University of California, San Diego
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Bipolar Disorder focused on measuring cannabidiol, THC

Eligibility Criteria

18 Years - 50 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. For subjects in BD group, DSM-5 criteria for Bipolar Disorder as determined by the Structured Clinical Interview for DSM-5 (SCID).
  2. Young Mania Rating Scale (YMRS) < 12.
  3. Infrequent cannabis use as defined by a history of cannabis use and current use no more than 4 times per month.
  4. Willing to abstain from cannabis use for at least two days prior to the experimental visit.

Exclusion Criteria:

  1. Hamilton Depression Rating Scale (HDRS) score > 10.
  2. Suicidality. Exposure to cannabis does not lead to depression but it may be associated with suicidal thoughts and attempts. Therefore, the Center for Epidemiological Studies-Depression Scale (CES-D) subscale measuring suicidal ideation ("I wished I were dead". "I wanted to hurt myself") will be completed. Should any of these items be answered affirmatively, e.g., the subject has endorsed these items for at least 1-2 days in the last week, the subject will not be enrolled in the study.
  3. The Substance Abuse Module of the Diagnostic Interview Schedule for DSM-5 will be administered to exclude individuals with current substance use disorders.
  4. Clinically significant or unstable medical condition. Subjects will undergo a medical evaluation (H&P, toxicology screening, and for females of childbearing potential, pregnancy testing (utilizing a human chorionic gonadotropin (hCG) urine test). Individuals with significant cardiovascular disease (e.g., angina, myocardial infarction or stroke), hepatic or renal disease, uncontrolled hypertension, and chronic pulmonary disease (e.g., asthma, COPD), will be excluded. With respect to cardiovascular and pulmonary status, a clinician will screen participants with a tool developed for this purpose (Appendix 3 Cardiopulmonary Screen). Hepatic and renal disease will be evaluated with liver and renal function laboratory tests. Females who are pregnant or lactating will be excluded.
  5. Infections - evidence of skin infection at lumbar puncture site.
  6. To avoid confounding of cognitive testing, a neurological disorder such as seizures, stroke, Parkinson's disease, dementia, or a history of head injury with loss of consciousness for at least 15 minutes will be excluded.
  7. Unwilling to refrain from driving or operate heavy machinery for four hours after consuming study medication. This criterion is consistent with current expert recommendations on driving following the use of cannabis.
  8. Additionally, because the hBPM paradigm requires participants to be ambulatory, those who cannot ambulate independently (e.g., require a wheelchair) or those who have a motor disease (e.g., multiple sclerosis, cerebral palsy) will be excluded.
  9. A previous adverse reaction to cannabinoids will be cause for exclusion as will a historical diagnosis of cannabis use disorder.
  10. Positive result on Draeger 5000 test indicating recent cannabis use.
  11. Unwillingness to prevent pregnancy during the cannabinoid administration portion of the study (using birth control in female participants of child-bearing age) Acceptable methods of birth control are: oral contraceptive pills, diaphragm, condom, progestin implant, intrauterine contraceptive device, sterilization, etc.
  12. Any active opportunistic infection or malignant condition requiring acute treatment.

Sites / Locations

  • UC San Diego Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Bipolar Disorder

Healthy Volunteers

Arm Description

adults with bipolar disorder

adults with no psychiatric disease

Outcomes

Primary Outcome Measures

Score on Iowa Gambling Task
This is an experimental measure and not a scale with specific anchor points. Lower scores reflect increased risk-taking
Score on Progressive Ratio Test
This is an experimental measure and not a scale with specific anchor points. Higher scores indicate increased willingness to work for a reward
Scores on Probabilistic Learning Task
This is an experimental measure and not a scale with specific anchor points. Measures decision-making strategies such as win-stay, lose-shift.
Scores on Continuous Performance Task
This is an experimental measure and not a scale with specific anchor points. Higher scores reflect better attention and ability to discriminate important information from unimportant information
Percent Prepulse Inhibition (PPI)
This is a physiological measure and not a scale with specific anchor points. Higher percent PPI reflects better sensorimotor gating
motor activity in the human Behavioral Pattern Monitor
This is an experimental measure and not a scale with specific anchor points. Subjects' behavior in an open field (a room filled with novel objects) is quantified over a 15-minute period via amount of motor activity as measured by a wearable accelerometer. Increased motor activity reflects increased tendency to engage in exploratory behavior.
object interactions in the human Behavioral Pattern Monitor
This is an experimental measure and not a scale with specific anchor points. Subjects' behavior in an open field (a room filled with novel objects) is quantified over a 15-minute period via video ratings that quantify number of interactions with novel objects. Increased object interactions reflects increased novelty-seeking behavior.
cerebrospinal fluid levels of anandamide
Reflects increased availability of the endogenous cannabinoid anandamide in the brain

Secondary Outcome Measures

Full Information

First Posted
January 8, 2020
Last Updated
May 8, 2023
Sponsor
University of California, San Diego
Collaborators
National Institute on Drug Abuse (NIDA)
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1. Study Identification

Unique Protocol Identification Number
NCT04231643
Brief Title
Effects of Cannabis on Cognition and Endocannabinoid Levels in Bipolar Disorder Patients and Healthy Volunteers
Official Title
A Randomized, Controlled Trial of Cannabis in Bipolar Disorder Patients and Healthy Volunteers Evaluating Cognition and Endocannabinoid Levels
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 1, 2021 (Actual)
Primary Completion Date
February 28, 2024 (Anticipated)
Study Completion Date
February 28, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of California, San Diego
Collaborators
National Institute on Drug Abuse (NIDA)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Cannabis use is associated with younger age at onset of bipolar disorder, poor outcome, and more frequent manic episodes, but the effects of cannabis on cognition are less clear. Contrary to reports among non-psychiatric patients, cannabis may improve cognition among people with bipolar disorder. Nevertheless, no study to date has systematically tested the acute effects of cannabis on cognition in bipolar disorder. Therefore, the investigators propose to determine the effects of oral cannabinoid administration on cognitive domains relevant to bipolar disorder, e.g., arousal, decision making, cognitive control, inhibition, and temporal perception (sense of timing). In addition, the investigators will evaluate different doses of the two major components of cannabis, cannabidiol and ∆9-tetrahydrocannabinol, and compare them to placebo on these neurocognitive measures. The investigators will also test the effects of acute exposure to cannabinoids on cerebrospinal levels of anandamide and homovanillic acid - markers of endocannabinoid and dopamine activity in the brain, respectively. These studies will provide information that effectively bridges the fields of addiction and general psychiatry, informing treatment development for co-morbid substance abuse and psychiatric disorders.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bipolar Disorder
Keywords
cannabidiol, THC

7. Study Design

Primary Purpose
Basic Science
Study Phase
Early Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
144 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Bipolar Disorder
Arm Type
Experimental
Arm Description
adults with bipolar disorder
Arm Title
Healthy Volunteers
Arm Type
Active Comparator
Arm Description
adults with no psychiatric disease
Intervention Type
Drug
Intervention Name(s)
Dronabinol
Intervention Description
one-time oral administration of 5 mg dronabinol
Intervention Type
Drug
Intervention Name(s)
Epidiolex
Intervention Description
one-time oral administration of 600 mg Epidiolex
Intervention Type
Drug
Intervention Name(s)
Placebos
Intervention Description
one-time oral administration of placebo
Primary Outcome Measure Information:
Title
Score on Iowa Gambling Task
Description
This is an experimental measure and not a scale with specific anchor points. Lower scores reflect increased risk-taking
Time Frame
one day
Title
Score on Progressive Ratio Test
Description
This is an experimental measure and not a scale with specific anchor points. Higher scores indicate increased willingness to work for a reward
Time Frame
one day
Title
Scores on Probabilistic Learning Task
Description
This is an experimental measure and not a scale with specific anchor points. Measures decision-making strategies such as win-stay, lose-shift.
Time Frame
one day
Title
Scores on Continuous Performance Task
Description
This is an experimental measure and not a scale with specific anchor points. Higher scores reflect better attention and ability to discriminate important information from unimportant information
Time Frame
one day
Title
Percent Prepulse Inhibition (PPI)
Description
This is a physiological measure and not a scale with specific anchor points. Higher percent PPI reflects better sensorimotor gating
Time Frame
one day
Title
motor activity in the human Behavioral Pattern Monitor
Description
This is an experimental measure and not a scale with specific anchor points. Subjects' behavior in an open field (a room filled with novel objects) is quantified over a 15-minute period via amount of motor activity as measured by a wearable accelerometer. Increased motor activity reflects increased tendency to engage in exploratory behavior.
Time Frame
one day
Title
object interactions in the human Behavioral Pattern Monitor
Description
This is an experimental measure and not a scale with specific anchor points. Subjects' behavior in an open field (a room filled with novel objects) is quantified over a 15-minute period via video ratings that quantify number of interactions with novel objects. Increased object interactions reflects increased novelty-seeking behavior.
Time Frame
one day
Title
cerebrospinal fluid levels of anandamide
Description
Reflects increased availability of the endogenous cannabinoid anandamide in the brain
Time Frame
one day

10. Eligibility

Sex
All
Gender Based
Yes
Gender Eligibility Description
Participants will be asked about which gender they identify with
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: For subjects in BD group, DSM-5 criteria for Bipolar Disorder as determined by the Structured Clinical Interview for DSM-5 (SCID). Young Mania Rating Scale (YMRS) < 12. Infrequent cannabis use as defined by a history of cannabis use and current use no more than 4 times per month. Willing to abstain from cannabis use for at least two days prior to the experimental visit. Exclusion Criteria: Hamilton Depression Rating Scale (HDRS) score > 10. Suicidality. Exposure to cannabis does not lead to depression but it may be associated with suicidal thoughts and attempts. Therefore, the Center for Epidemiological Studies-Depression Scale (CES-D) subscale measuring suicidal ideation ("I wished I were dead". "I wanted to hurt myself") will be completed. Should any of these items be answered affirmatively, e.g., the subject has endorsed these items for at least 1-2 days in the last week, the subject will not be enrolled in the study. The Substance Abuse Module of the Diagnostic Interview Schedule for DSM-5 will be administered to exclude individuals with current substance use disorders. Clinically significant or unstable medical condition. Subjects will undergo a medical evaluation (H&P, toxicology screening, and for females of childbearing potential, pregnancy testing (utilizing a human chorionic gonadotropin (hCG) urine test). Individuals with significant cardiovascular disease (e.g., angina, myocardial infarction or stroke), hepatic or renal disease, uncontrolled hypertension, and chronic pulmonary disease (e.g., asthma, COPD), will be excluded. With respect to cardiovascular and pulmonary status, a clinician will screen participants with a tool developed for this purpose (Appendix 3 Cardiopulmonary Screen). Hepatic and renal disease will be evaluated with liver and renal function laboratory tests. Females who are pregnant or lactating will be excluded. Infections - evidence of skin infection at lumbar puncture site. To avoid confounding of cognitive testing, a neurological disorder such as seizures, stroke, Parkinson's disease, dementia, or a history of head injury with loss of consciousness for at least 15 minutes will be excluded. Unwilling to refrain from driving or operate heavy machinery for four hours after consuming study medication. This criterion is consistent with current expert recommendations on driving following the use of cannabis. Additionally, because the hBPM paradigm requires participants to be ambulatory, those who cannot ambulate independently (e.g., require a wheelchair) or those who have a motor disease (e.g., multiple sclerosis, cerebral palsy) will be excluded. A previous adverse reaction to cannabinoids will be cause for exclusion as will a historical diagnosis of cannabis use disorder. Positive result on Draeger 5000 test indicating recent cannabis use. Unwillingness to prevent pregnancy during the cannabinoid administration portion of the study (using birth control in female participants of child-bearing age) Acceptable methods of birth control are: oral contraceptive pills, diaphragm, condom, progestin implant, intrauterine contraceptive device, sterilization, etc. Any active opportunistic infection or malignant condition requiring acute treatment.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Elizabeth Peek, BA
Phone
6195436575
Email
eypeek@health.ucsd.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
William Perry, PhD
Organizational Affiliation
UCSD
Official's Role
Principal Investigator
Facility Information:
Facility Name
UC San Diego Medical Center
City
San Diego
State/Province
California
ZIP/Postal Code
92103
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Elizabeth Peek, BA
Phone
619-543-6575
Email
eypeek@health.ucsd.edu

12. IPD Sharing Statement

Plan to Share IPD
No

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Effects of Cannabis on Cognition and Endocannabinoid Levels in Bipolar Disorder Patients and Healthy Volunteers

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