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CompletedNCT05115513NHTSA-IIUpdated Oct 9, 2025

Standardized Field Test for Marijuana Impairment II

A Phase 1 interventional study of Medium THC and Placebo THC in Marijuana Impairment, sponsored by Yale University. Completed at 1 site in United States. Open to participants aged 18 Years to 55 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-10-09.

Sponsored by Yale University · Phase 1, Interventional, and Other

From the registry’s dates

  • Primary completion was Aug 2023, 3 years 1 month ago, and no results have been posted to the registry.
Phase
Phase 1
Study type
Interventional
Enrollment
41
Allocation
Non-randomized
Ages
18 Years to 55 Years
Sex
All
01

Study summary

This research responds to NHTSA's request with a proposal to increase our understanding of smoked cannabis' (CNB's) acute effects on driving-relevant cognition and simulated driving performance, the persistence of these deficits over the hours after use, and the influence of prior experience with CNB on these effects. This extension study will aim to further investigate marijuana impaired behavior, using a similar design to our previous NHTSA Examine the Feasibility of a Standardized Field Test for Marijuana Impairment and the prior NIDA Neuroscience of Marijuana-Impaired Driving award, that used similar techniques and measures to quantify marijuana impaired automobile driving. We will be utilizing tasks and assessments that were shown to be strong indicators for cognitive and driving impairment in our NHTSA study.

Read the detailed description

The proposed study was based upon a careful and thorough review of the scientific literature describing CNB effects on cognitive test performance and driving, as well as current state-of-knowledge on the sensitivity of biological assays for identifying recent CNB use. The study will carefully characterize the persistence of CNB's acute effects on cognitive test performance and driving over a several-hour time span. This will allow us to identify the point at which any effects of CNB intoxication driving-related cognitive tests, and driving performance cannot be distinguished from normal, i.e., the first step towards establishing standards for legal and social policy. The data obtained from simulated driving, cognitive tests, and biological assays of THC will be used in analyses aimed at identifying what tests or combination of tests predict both recent use and driving impairment risk.

This study will consist of 2 days (screening visit and dose visit). In a non-randomized, single blinded study, we will dose participants with placebo and high THC marijuana, about an hour apart, using paced inhalation through a vaporizer, an efficient means of delivering a standard THC dose. Participants will be told that the order they receive the doses will be random but they will always receive the placebo first, followed by the high dose. This will allow for standardization across all subjects and comparative values between placebo and drug. After inhaling the placebo dose, participants will be asked to complete one round of cognitive testing and a shortened version of the driving simulator (10 mins vs 30 mins). Approximately one hour post placebo dose, subjects will be administered high THC marijuana. Following this dosing, we will assess impairment through cognitive testing as well as a simulated driving test and neuropsychological tests. Samples of blood will also be collected at multiple time points throughout the study visits to be measured for THC concentration and its metabolites. This allows clarification between the relationship of impairment, as well as subjective and objective intoxication, and levels of THC and it's metabolites in the users system.

02

Conditions studied

  • Marijuana Impairment

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Keywords

  • Marijuana
  • THC
  • Cannabis
  • Driving
  • Impairment
  • Intoxication
03

In context

Marijuana Abuse

517 studies on the registry are indexed under Marijuana Abuse; 114 are open to participants now.

This study's enrollment of 41 is below the median of 60 across 421 interventional studies indexed under Marijuana Abuse.

Browse Marijuana Abuse studies →

Lead sponsor

Yale University is the lead sponsor of 1,724 studies on the registry; 298 are open to participants now.

Of its 210 completed or terminated interventional studies of FDA-regulated products, 126 (60%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 55 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • 18-55 yrs/ old
  • Current driver's license and history of repeated highway vehicle driving experience (at least 2 years)
  • Recent, recurrent CNB use and felt high when used
  • Able to read, speak, and understand English
  • Able and willing to provide written informed consent, and willing to commit to the study protocol

Exclusion criteria

Exclusion Criteria:

  • Current marijuana tolerance, desire to cut down, or cravings to use during periods of abstinence
  • New CNB users who have not used at least once during their lifetime.
  • Positive screen for drug and alcohol (except THC) on test day will result in rescheduling the appointment
  • Former CNB users who are abstaining
  • Pregnancy, breastfeeding, and ineffective birth control methods.
  • History of adverse psychological or medical effects following cannabis use
  • serious medical, neuro-ophthalmological, or neurological illness (i.e. cancer, seizure disorders, encephalopathy)
  • History of head trauma with loss of consciousness > 30 minutes or concussion lasting 30 days.
  • IQ \<80 on the Wechsler Abbreviated Scale of Intelligence
  • Inability to comprehend written instructions using the WRAT 4 reading achievement test
  • Any medical/neurological condition that could compromise neurocognitive performance (i.e. epilepsy, multiple sclerosis, fetal alcohol syndrome)
  • Uncontrolled, persistent high blood pressure
  • Anyone deemed unsafe to study personnel for any reason
05

Study design

Phase
Phase 1
Primary purpose
Other
Allocation
Non-randomized
Intervention model
Crossover assignment
Masking
Single (Participant)
Enrollment
41 participants (actual)

Study arms

  • Experimental
    Placebo Marijuana

    Placebo Marijuana will be administered.

    Drug: Placebo THC

  • Experimental
    Medium THC Marijuana

    Medium THC marijuana will be administered.

    Drug: Medium THC

Interventions

  • DrugMedium THC

    Marijuana flower with medium THC

  • DrugPlacebo THC

    Marijuana flower with no THC

06

What researchers measure

Primary outcomes

  1. Marijuana induced performance changes on Cogstate Groton Maze Learning task.

    The Cogstate Groton Maze Learning task assesses spatial learning and memory, it will be administered prior to dosing and at various time points after dosing.

    Time frame: Post placebo at 30 minutes and post active dose administration at: 30 minutes, 60 minutes , 90 minutes, 120 minutes, 150 minutes, 180 minutes.

  2. Marijuana induced performance changes on Inquisit Maze Learning task.

    The Inquisit Maze Learning task assesses spatial learning and memory, it will be administered prior to dosing and at various time points after dosing.

    Time frame: Post placebo at 30 minutes and post active dose administration at: 30 minutes, 60 minutes , 90 minutes, 120 minutes, 150 minutes, 180 minutes.

  3. Marijuana induced performance changes on the Time Reproduction Task.

    The Time Reproduction Task assesses general motor coordination plus timing, it will be administered prior to dosing and at various time points after dosing.

    Time frame: Post placebo at 30 minutes and post active dose administration at: 30 minutes, 60 minutes , 90 minutes, 120 minutes, 150 minutes, 180 minutes.

Secondary outcomes

  1. Change in concentration of THC/metabolites in blood samples.

    Blood samples with be collected at 5 times throughout each day to assess for changes of THC and its metabolite levels.

    Time frame: Post placebo at 5 minutes and post active dose administration at: 30 minutes, 60 minutes , 90 minutes, 120 minutes, 150 minutes, 180 minutes.

  2. Change in performance on 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.

    Time frame: Post placebo at 10 minutes and post active dose administration at 210 minutes.

07

Study locations

1 site
  • Olin Neuropsychiatry Research Center
    Hartford, Connecticut 06106, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 9, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05115513
Lead sponsor
Yale University
Collaborators
National Highway Traffic Safety Administration (NHTSA), Hartford Hospital, National Institute on Drug Abuse (NIDA)
Responsible party
Godfrey Pearlson (Professor of Psychiatry and Neuroscience, Founding Director Olin Neuropsychiatry Research Center, Yale University) — Principal investigator
First posted
Nov 10, 2021
Start date
Aug 25, 2022
Primary completion
Aug 21, 2023
Completion
Aug 21, 2023
Last update
Oct 9, 2025

Study contacts

Godfrey Pearlson, M.D
principal investigator · Yale University

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Oct 2025. You cannot join it, but the record below documents what was studied.

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