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Cannabis Consumption and Driving Impairment Assessment on a Closed Course

Primary Purpose

Cannabis Smoking, Driving Impaired

Status
Recruiting
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Active smoked cannabis
Placebo smoked cannabis
Sponsored by
Bayliss J. Camp, PhD
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Cannabis Smoking

Eligibility Criteria

21 Years - 55 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Possessing a valid California driver's license Cannabis use in the past six months Willing and able to abstain from alcohol, cannabis, and other recreational drugs for 24 hours prior to scheduled participation Willing and able to avoid driving and operating heavy machinery for at least four hours after participation Residence within approximately 15 miles of the study site Possessing the capacity to provide informed consent Exclusion Criteria: Completion of a roadside sobriety test during the previous 12 months Physical or psychological conditions that can be exacerbated by cannabis use, or for which cannabis use is contraindicated Potential presence of Cannabis Use Disorder as assessed by a modified version of the Cannabis Use Disorder Identification Test Potential presence of Substance Use Disorder as assessed by a modified version of the Drug Abuse Screening Test Pregnancy or breastfeeding reported Unwillingness to be transported by taxi Having been convicted of Driving Under the Influence (DUI) within five years prior to scheduled participation Parole or probation status One or more felony convictions on record involving aggressive or dangerous criminal activity Any of the following at the time of the experimental session: breath alcohol content of .01% or greater; positive pregnancy test; cannabis consumption considered unsafe following medical checkup by the study nurse; or driving test behavior considered hazardous by the driving examiner

Sites / Locations

  • California Department of Motor Vehicles HeadquartersRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Placebo Comparator

No Intervention

Arm Label

Active Smoked Cannabis

Placebo Smoked Cannabis

Control

Arm Description

Participants in this arm will smoke an active cannabis cigarette containing 18.16% Δ9-tetrahydrocannabinol (THC). The smoking will occur at each participant's preferred pace, but will be limited to a maximum ten-minute period. While individual doses vary in this type of paradigm (ad libitum dosing), the anticipated dose of THC within the cannabis condition can be approximated by the following formula: (700 mg of cannabis) x [% of cigarette smoked; maximum of 70% (allowing room to hold the cigarette)] x (% THC). Therefore, the maximum dose in this arm is 700 mg x 70% x 18.2% = 89.18 mg of THC. Individual participants will only take part in the study under a single condition and receive the active cannabis once. Bulk cannabis for this arm will be provided by the National Institute on Drug Abuse Drug Supply Program; cannabis cigarettes will be prepared and prescribed by the Research Pharmacy of the University of California, San Diego.

Participants in this arm will smoke a placebo cannabis cigarette containing <.01 THC. The smoking will occur at each participant's preferred pace, but will be limited to a maximum ten-minute period. Individual participants will only take part in the study under a single condition and receive the placebo cannabis once. Bulk placebo for this arm will be provided by the National Institute on Drug Abuse Drug Supply Program; placebo cannabis cigarettes will be prepared and prescribed by the Research Pharmacy of the University of California, San Diego.

Participants in this arm receive no cannabis. Individual participants will only take part in the study under a single condition.

Outcomes

Primary Outcome Measures

Modified Driving Performance Examination (MDPE)
The MDPE driving test, developed for this study, is administered once per participant per experimental session. It occurs after the assigned intervention (i.e., drug administration) and it is primarily scored dichotomously (pass versus fail).
Advanced Roadside Impaired Driving Enforcement (ARIDE) battery
The ARIDE battery is not a scale but a series of roadside behavioral assessments used by law enforcement officers to help them detect impaired driving: (1) pulse check, (2) Horizontal Gaze Nystagmus or HGN, (3) a test of distinct and sustained nystagmus, (4) vertical nystagmus, (5) lack of convergence test, (6) a check to see if eyes are bloodshot or watery, (7) Modified Romberg Balance Test, (8) Walk and Turn Test or WAT, (9) One Leg Stand Test or OLS, and some additional observations. The ARIDE battery occurs once per participant following the Modified Driving Performance Examination. The ARIDE battery is scored overall as pass versus fail by the officer conducting the test (in real-time).
Drug Recognition Expert (DRE) evaluation
The DRE evaluation is designed to help law enforcement officers identify whether an individual is generally impaired and, if so, which class of substance caused the impairment. The DRE evaluation occurs once per participant, following the ARIDE battery. It is scored by the officer conducting it in real-time as a judgment about state of impairment (impaired versus unimpaired), and, in the case of impairment, a judgment about the class of substance.

Secondary Outcome Measures

First blood draw (baseline)
The first blood sample is collected at baseline (after consent procedures and a medical checkup), roughly 25 minutes into the experimental session. This is before the assigned intervention (i.e., drug administration) and before any of the primary outcome measures occurs. All samples will undergo toxicological analyses to assess blood concentrations (in nanograms per milliliter) of cannabinoids, as well as the presence of other drugs (opioids, benzodiazepines, and stimulants).
Second blood draw (change from baseline)
The second blood sample is collected immediately after the assigned intervention (i.e., drug administration), around the time that THC concentration is expected to be at its peak. Most samples will undergo toxicological analyses to assess blood concentrations (in nanograms per milliliter) of cannabinoids and these results will be compared to those of the first blood draw. In the case of control participants whose first sample did not reveal the presence of cannabinoids, no further analyses will be conducted.
Third blood draw (change from baseline and second blood draw)
The third blood sample is collected after the Advanced Roadside Impaired Driving Enforcement (ARIDE) battery and immediately before the Drug Recognition Expert (DRE) evaluation. Most samples will undergo toxicological analyses to assess blood concentrations (in nanograms per milliliter) of cannabinoids and these results will be compared to those of the first and second blood draws. In the case of control participants whose first sample did not reveal the presence of cannabinoids, no further analyses will be conducted.

Full Information

First Posted
May 28, 2021
Last Updated
September 26, 2023
Sponsor
Bayliss J. Camp, PhD
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1. Study Identification

Unique Protocol Identification Number
NCT06059677
Brief Title
Cannabis Consumption and Driving Impairment Assessment on a Closed Course
Official Title
Cannabis Consumption and Driving Impairment Assessment on a Closed Course
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 3, 2023 (Anticipated)
Primary Completion Date
December 31, 2024 (Anticipated)
Study Completion Date
December 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Bayliss J. Camp, PhD

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
In a true experiment, roughly 300 volunteer participants will smoke active cannabis, a corresponding placebo, or no substance at all (control). Next, participants will complete a drive test and then be observed by actual California Highway Patrol (CHP) officers who will attempt to classify participants as impaired or unimpaired. CHP Officers will evaluate participants in the context of driving (i.e., while following participants in an actual patrol car), as part of a roadside behavioral assessment (i.e., the Advanced Roadside Impaired Driving Enforcement, or ARIDE, battery, which includes Standardized Field Sobriety Tests, or SFSTs), and as part of a Drug Recognition Expert (DRE) evaluation conducted indoors.
Detailed Description
The easing of restrictions on the use of cannabis for recreational purposes presents a new challenge for policing of impaired driving, which is to say Driving Under the Influence of Drugs (DUI-D), specifically cannabis. In particular, it is not entirely clear how well the tools used by law enforcement officers to detect driving impairment (e.g., behavioral instruments such as the SFSTs, as included in the ARIDE battery) work for identifying cannabis-induced driving impairment specifically. While these instruments are designed to help officers identify driving impairment in general (irrespective of cause), prior empirical validation work has almost exclusively involved alcohol-induced impairment. This study will be conducted within a realistic, closed-course driving environment and it seeks to validate the same instruments currently used by law enforcement to detect cannabis-induced driving impairment against a second, independent, behavioral standard for driving impairment: a comprehensive driver evaluation adapted from the same set of driver tests that Californians must pass upon application for an original license, or (in certain instances) when referred to the Department of Motor Vehicles (DMV) for evaluation of their ability to safely operate a non-commercial class of motor vehicle (here referred to as the Modified Driver Performance Evaluation or MDPE). This study seeks to answer the following research questions: I. How accurately do behavioral assessments used by officers distinguish between drivers impaired by cannabis and drivers not impaired by cannabis? II. How does cannabis affect real-world (as opposed to simulated) driving performance?

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cannabis Smoking, Driving Impaired

7. Study Design

Primary Purpose
Other
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Model Description
This study is a true experiment in a naturalistic setting designed to maximize ecological validity, that is, designed so that the findings can be expected to generalize to their real-world application of detecting impaired driving. The study features a randomized between-subjects design, in which the main independent variable (Substance) has three levels: active cannabis vs. placebo vs. control (i.e., no substance).
Masking
ParticipantInvestigatorOutcomes Assessor
Masking Description
Participants are blind to condition assignment, meaning they are not told in advance which version of the procedure they will experience. While those assigned to the true control condition will obviously realize this during the session, remaining participants are not informed whether the cigarette they smoke contains active cannabis or placebo. Similarly, the experimenters will necessarily become aware of which individuals are in the control conditions, however, they do not know which of the remaining participants are assigned to active cannabis versus placebo conditions (i.e., the active vs. placebo cannabis cigarettes are not labeled as such). Most importantly, outcome assessors such as the officers and driving evaluators who supply the ratings that comprise the focal dependent variables will be completely blind to experimental condition, so that there is no straightforward means by which experimenter bias could affect data collected for those variables.
Allocation
Randomized
Enrollment
300 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Active Smoked Cannabis
Arm Type
Experimental
Arm Description
Participants in this arm will smoke an active cannabis cigarette containing 18.16% Δ9-tetrahydrocannabinol (THC). The smoking will occur at each participant's preferred pace, but will be limited to a maximum ten-minute period. While individual doses vary in this type of paradigm (ad libitum dosing), the anticipated dose of THC within the cannabis condition can be approximated by the following formula: (700 mg of cannabis) x [% of cigarette smoked; maximum of 70% (allowing room to hold the cigarette)] x (% THC). Therefore, the maximum dose in this arm is 700 mg x 70% x 18.2% = 89.18 mg of THC. Individual participants will only take part in the study under a single condition and receive the active cannabis once. Bulk cannabis for this arm will be provided by the National Institute on Drug Abuse Drug Supply Program; cannabis cigarettes will be prepared and prescribed by the Research Pharmacy of the University of California, San Diego.
Arm Title
Placebo Smoked Cannabis
Arm Type
Placebo Comparator
Arm Description
Participants in this arm will smoke a placebo cannabis cigarette containing <.01 THC. The smoking will occur at each participant's preferred pace, but will be limited to a maximum ten-minute period. Individual participants will only take part in the study under a single condition and receive the placebo cannabis once. Bulk placebo for this arm will be provided by the National Institute on Drug Abuse Drug Supply Program; placebo cannabis cigarettes will be prepared and prescribed by the Research Pharmacy of the University of California, San Diego.
Arm Title
Control
Arm Type
No Intervention
Arm Description
Participants in this arm receive no cannabis. Individual participants will only take part in the study under a single condition.
Intervention Type
Drug
Intervention Name(s)
Active smoked cannabis
Other Intervention Name(s)
marijuana, cannabis sativa, C. sativa L., C. sativa. Cannabis sativa L., Cannabis indica, C. indica
Intervention Description
Assessment of active cannabis smoking and driving impairment
Intervention Type
Drug
Intervention Name(s)
Placebo smoked cannabis
Other Intervention Name(s)
marijuana placebo, cannabis placebo, placebo marijuana, placebo cannabis
Intervention Description
Assessment of placebo cannabis smoking and driving impairment
Primary Outcome Measure Information:
Title
Modified Driving Performance Examination (MDPE)
Description
The MDPE driving test, developed for this study, is administered once per participant per experimental session. It occurs after the assigned intervention (i.e., drug administration) and it is primarily scored dichotomously (pass versus fail).
Time Frame
Conducted an average of 35 minutes after the assigned intervention is completed.
Title
Advanced Roadside Impaired Driving Enforcement (ARIDE) battery
Description
The ARIDE battery is not a scale but a series of roadside behavioral assessments used by law enforcement officers to help them detect impaired driving: (1) pulse check, (2) Horizontal Gaze Nystagmus or HGN, (3) a test of distinct and sustained nystagmus, (4) vertical nystagmus, (5) lack of convergence test, (6) a check to see if eyes are bloodshot or watery, (7) Modified Romberg Balance Test, (8) Walk and Turn Test or WAT, (9) One Leg Stand Test or OLS, and some additional observations. The ARIDE battery occurs once per participant following the Modified Driving Performance Examination. The ARIDE battery is scored overall as pass versus fail by the officer conducting the test (in real-time).
Time Frame
Conducted an average of 65 minutes after the assigned intervention is completed.
Title
Drug Recognition Expert (DRE) evaluation
Description
The DRE evaluation is designed to help law enforcement officers identify whether an individual is generally impaired and, if so, which class of substance caused the impairment. The DRE evaluation occurs once per participant, following the ARIDE battery. It is scored by the officer conducting it in real-time as a judgment about state of impairment (impaired versus unimpaired), and, in the case of impairment, a judgment about the class of substance.
Time Frame
Conducted an average of 90 minutes after the assigned intervention is completed.
Secondary Outcome Measure Information:
Title
First blood draw (baseline)
Description
The first blood sample is collected at baseline (after consent procedures and a medical checkup), roughly 25 minutes into the experimental session. This is before the assigned intervention (i.e., drug administration) and before any of the primary outcome measures occurs. All samples will undergo toxicological analyses to assess blood concentrations (in nanograms per milliliter) of cannabinoids, as well as the presence of other drugs (opioids, benzodiazepines, and stimulants).
Time Frame
Conducted 15 minutes before the assigned intervention.
Title
Second blood draw (change from baseline)
Description
The second blood sample is collected immediately after the assigned intervention (i.e., drug administration), around the time that THC concentration is expected to be at its peak. Most samples will undergo toxicological analyses to assess blood concentrations (in nanograms per milliliter) of cannabinoids and these results will be compared to those of the first blood draw. In the case of control participants whose first sample did not reveal the presence of cannabinoids, no further analyses will be conducted.
Time Frame
Conducted immediately after the assigned intervention is completed.
Title
Third blood draw (change from baseline and second blood draw)
Description
The third blood sample is collected after the Advanced Roadside Impaired Driving Enforcement (ARIDE) battery and immediately before the Drug Recognition Expert (DRE) evaluation. Most samples will undergo toxicological analyses to assess blood concentrations (in nanograms per milliliter) of cannabinoids and these results will be compared to those of the first and second blood draws. In the case of control participants whose first sample did not reveal the presence of cannabinoids, no further analyses will be conducted.
Time Frame
Conducted an average of 85 minutes after the assigned intervention is completed.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Possessing a valid California driver's license Cannabis use in the past six months Willing and able to abstain from alcohol, cannabis, and other recreational drugs for 24 hours prior to scheduled participation Willing and able to avoid driving and operating heavy machinery for at least four hours after participation Residence within approximately 15 miles of the study site Possessing the capacity to provide informed consent Exclusion Criteria: Completion of a roadside sobriety test during the previous 12 months Physical or psychological conditions that can be exacerbated by cannabis use, or for which cannabis use is contraindicated Potential presence of Cannabis Use Disorder as assessed by a modified version of the Cannabis Use Disorder Identification Test Potential presence of Substance Use Disorder as assessed by a modified version of the Drug Abuse Screening Test Pregnancy or breastfeeding reported Unwillingness to be transported by taxi Having been convicted of Driving Under the Influence (DUI) within five years prior to scheduled participation Parole or probation status One or more felony convictions on record involving aggressive or dangerous criminal activity Any of the following at the time of the experimental session: breath alcohol content of .01% or greater; positive pregnancy test; cannabis consumption considered unsafe following medical checkup by the study nurse; or driving test behavior considered hazardous by the driving examiner
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dario LM Sacchi, PhD
Phone
(916) 818 5312
Email
dario.sacchi2@dmv.ca.gov
First Name & Middle Initial & Last Name or Official Title & Degree
Dario L Sacchi, PhD
Phone
(916) 914 8118
Email
Dario.Sacchi2@dmv.ca.gov
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bayliss J Camp, PhD
Organizational Affiliation
California Department of Motor Vehicles
Official's Role
Principal Investigator
Facility Information:
Facility Name
California Department of Motor Vehicles Headquarters
City
Sacramento
State/Province
California
ZIP/Postal Code
95818-2606
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Bayliss J Camp, PhD
Phone
916-818-5312
Email
alicepitt7@gmail.com

12. IPD Sharing Statement

Plan to Share IPD
No

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Cannabis Consumption and Driving Impairment Assessment on a Closed Course

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