Not provided
| ID | Type | Description | Link |
|---|---|---|---|
| 1R01DA038807-01A1 | U.S. NIH Grant/Contract | View source |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Class |
|---|---|
| Hartford Hospital | OTHER |
| National Institute on Drug Abuse (NIDA) | NIH |
| Montana State University | OTHER |
| Maastricht University |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Marijuana is one of the most widely used substances. However, marijuana intoxication is not fully understood in relation to driving. This study will help the investigators learn more about the potential impairments related to marijuana intoxicated driving. A combination of MRI and neuropsychological tests (which are computer and paper/pencil tasks) will be used to measure intoxication and impairment. This study will also assess levels of marijuana in blood and saliva samples. This study takes place in Hartford, Connecticut.
Cannabis is a commonly abused drug whose use cuts across social class, is linked to cognitive impairment, and may be a major contributor to intoxication-related accidents - either alone or with alcohol. However, cannabis intoxication is little studied in relation to driving compared to alcohol. Not only does the current NHTSA Strategic Plan for Behavioral Research prioritize understanding how drugs other than alcohol contribute to traffic crashes, it has recently become more pressing to understand the effects of cannabis because of increasing rates of legalized medical and/or recreational use, that will likely result in more cannabis intoxicated drivers. Social and legal policy will be unable to effectively address the many concerns about driving safety raised by more frequent and widespread use of cannabis without new research to better determine the parameters within which cannabis use does, or does not, increase automobile accident risk. The purpose of this study is to better describe specific, driving-related cognitive impairments caused by acute cannabis intoxication, their persistence over time, underlying functional brain anatomy, and relationship to performance on a state-of the art validated simulated driving task in which the investigators have prior experience. In a randomized, counterbalanced, double-blinded fashion, the investigators will administer two cannabis doses and placebo of smoked cannabis (paced inhalation using a vaporizer) to 48 regular cannabis users and 48 occasional cannabis users on 3 separate occasions. Following cannabis dosing cognitive and driving impairment will be assessed longitudinally for several hours using a combination of fMRI and neuropsychological tests, to clarify relationships between subjective and objective measures of intoxication and of impairment, that include expert assessment of THC and its metabolite levels in blood and saliva. This study takes place in Hartford, Connecticut.
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Regular Users | Experimental | People who use marijuana regularly will be given a low dose THC marijuana, high dose THC marijuana and placebo marijuana, in a randomized order, at the study visits. |
|
| Occasional Users | Experimental | People who use marijuana occasionally will be given a low dose THC marijuana, high dose THC marijuana and placebo marijuana, in a randomized order, at the study visits. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Low dose THC marijuana | Drug |
|
| |
| Measure | Description | Time Frame |
|---|---|---|
| Change in performance on fMRI simulated driving Gap Acceptance Task | The Gap Acceptance Task measures strategic control of the vehicle. Strategic control of the vehicle is measured by size of headway gaps that the participant chooses in pulling out into a stream of traffic. | Post drug administration at: 30 min, 3 hours and 5.25 hours |
| Change in performance on fMRI simulated driving Road Tracking Task. | The Road Tracking Task measures operational control of the vehicle. Operational control is measured by standard deviation of lane position from the center point of the lane. | Post drug administration at: 30 min, 3 hours and 5.25 hours |
| Change in performance on fMRI simulated driving Car Following Task. | The Car Following Task measures tactical control of the vehicle. Tactical control of the vehicle is measured by following distance from a lead vehicle. | Post drug administration at: 30 min, 3 hours and 5.25 hours |
| Change in concentration of THC/metabolites in oral fluid tested using Draeger Drug Detection Kits | Saliva samples will be taken at 8 total time points throughout the day using the Draeger Drug Detection kits to assess for changes in concentration of THC and its metabolites. | Baseline and post drug administration at: 5 min, 20 min, 1 hr 10 min, 1 hr 45 min, 2 hrs 30 min, 4 hrs, and 6 hrs 30 min, |
| Change in concentration of THC/metabolites in oral fluid tested using Quantisal Oral Fluid Collection devices. | Saliva samples will be taken at 8 total time points throughout the day using the Quantisal Oral Fluid Collection devices to assess for changes in concentration of THC and its metabolites. | Baseline and post drug administration at: 5 min, 20 min, 1 hr 10 min, 1 hr 45 min, 2 hrs 30 min, 4 hrs, and 6 hrs 30 min, |
| Measure | Description | Time Frame |
|---|---|---|
| Change in performance on fMRI Set-Shifting paradigm. | The set shifting paradigm measures attentional and executive domains. | Post drug administration at: 1.25 hours, 3.5 hours and 6 hours |
| Change in performance on fMRI Time Estimation paradigm. |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Godfrey Pearlson | Founding Director Olin Research Center; Professor Yale University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Olin Neuropsychiatry Research Center | Hartford | Connecticut | 06106 | United States |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| ID | Term |
|---|---|
| D002189 | Marijuana Abuse |
| ID | Term |
|---|---|
| D019966 | Substance-Related Disorders |
| D064419 | Chemically-Induced Disorders |
| D001523 | Mental Disorders |
Not provided
Not provided
| ID | Term |
|---|---|
| D013759 | Dronabinol |
| C587251 | nabiximols |
| ID | Term |
|---|---|
| D002186 | Cannabinoids |
| D013729 | Terpenes |
| D006838 | Hydrocarbons |
| D009930 | Organic Chemicals |
Not provided
Not provided
| OTHER |
| The Mind Research Network | OTHER |
Not provided
Not provided
Not provided
Not provided
| High dose THC marijuana |
| Drug |
|
|
| Placebo marijuana | Drug |
|
|
| Change in concentration of THC/metabolites in blood samples. | Blood samples will be taken at 8 total time points throughout the day to assess for changes in concentration of THC and its metabolites. | Baseline and post drug administration at: 5 min, 20 min, 1 hr 10 min, 1 hr 45 min, 2 hrs 30 min, 4 hrs, and 6 hrs 30 min, |
| Marijuana performance changes on the Critical Tracking Task. | The Critical Tracking Task assesses visuomotor tracking, it will be administered prior to dosing and at various time points after dosing. | Post drug administration at two of the following time points (which varies dependent on the visit day): 2 hours; 4.25 hours; 6.5 hours |
| Marijuana performance changes on the Tower of London task. | The Tower of London is a task that assesses executive functioning, it will be administered prior to dosing and at various time points after dosing. | Post drug administration at two of the following time points (which varies dependent on the visit day): 2 hours; 4.25 hours; 6.5 hours |
| Marijuana performance changes on the Cogstate 1-back/2-back task. | The Cogstate 1-back/2-back task assesses working memory, it will be administered prior to dosing and at various time points after dosing. | Post drug administration at two of the following time points (which varies dependent on the visit day): 2 hours; 4.25 hours; 6.5 hours |
| Marijuana performance changes on the Cogstate Detection Task. | The Cogstate Detection Task assesses processing speed, it will be administered prior to dosing and at various time points after dosing. | Post drug administration at two of the following time points (which varies dependent on the visit day): 2 hours; 4.25 hours; 6.5 hours |
| Marijuana performance changes on the Cogstate Set Shifting Task. | The Cogstate Set Shifting Task assesses executive functioning, it will be administered prior to dosing and at various time points after dosing. | Post drug administration at two of the following time points (which varies dependent on the visit day): 2 hours; 4.25 hours; 6.5 hours |
The time estimation paradigm measures misjudgment of time intervals based on participant responses indicating whether one time interval was the same, longer or shorter than the previous time interval.
| Post drug administration at: 1.25 hours, 3.5 hours and 6 hours |