Novel Approaches to Assessing Cannabis Impaired Driving (NAACID) (NAACID)

April 20, 2026 updated by: Ashley Brooks-Russell, Colorado School of Public Health

Novel Approaches to Assessing Cannabis Impaired Driving

Researchers at the University of Colorado Anschutz Medical Campus, Colorado School of Public Health, and Injury & Violence Prevention Center want to learn more about how people are affected by cannabis in different ways. The study will use a driving simulator to compare the driving performance of adults who use cannabis daily, occasionally or have not recently used cannabis.

Study Overview

Status

Completed

Conditions

Study Type

Observational

Enrollment (Actual)

207

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Colorado
      • Denver, Colorado, United States, 80220
        • Driving Study Lab

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

N/A

Sampling Method

Non-Probability Sample

Study Population

Potential participants will be recruited from the general population.

Description

Inclusion Criteria:

  • The following are inclusion criteria for participants to be enrolled in any of the four phases of the study:

    1. Participants who are ≥21 years old and ≤55 years old
    2. Participants who are able to provide written, informed consent
    3. Participants with active healthcare coverage (including health insurance, Medicaid, etc.)
    4. Participants who are willing to complete up to two in-person study visits (one for Phases 1 & 2, and two for Phases 3 & 4), including up to two urine drug screens, two alcohol breathalyzer tests, and one urine pregnancy test (if applicable)
    5. Participants who agree to refrain from using non-prescription psychotropic drugs (e.g., ecstasy), hallucinogens, and synthetic cannabinoids during the study
    6. Participants who agree to refrain from drinking >3 alcoholic drinks the day prior to the data collection study visit (the single visit for Phases 1 & 2, and the second visit for Phases 3 & 4)
    7. Participants who agree to refrain from using any cannabis products for at least 8 hours prior to the data collection study visit (the single visit for Phases 1 & 2, and the second visit for Phases 3 & 4)
    8. Participants who are willing to provide and use their own cannabis product that has been procured from a licensed dispensary, is labeled with THC potency, and contains <2% CBD (cannabis use groups only; the single visit for Phases 1 & 2, and the second visit for Phases 3 & 4)
    9. Participants who agree to have a sober driver pick them up after the data collection study visit (cannabis use groups only; the single visit for Phases 1 & 2, and the second visit for Phases 3 & 4)
    10. Participants who take at least 2 inhalations ("hits") during their typical inhalational (smoking/vaporizing) sessions, or ingest at least 5 mg of THC when they consume edible cannabis products (cannabis use groups only)
    11. Participants who are willing to provide a sample of their cannabis to be independently tested for potency and terpene content (Phases 1, 3 & 4 only)

Exclusion Criteria:

  • The following are exclusion criteria for participants to be enrolled in any of the four phases of the study:

    1. Prisoners
    2. Participants who have nocturnal schedules (e.g., work night shifts)
    3. Participants with a history of abuse or addiction to substances other than cannabis (e.g., prescription and non-prescription pharmaceuticals, alcohol, or illicit drugs)
    4. Participants who have expressed an interest in substance abuse treatment within the 60 days prior to study enrollment
    5. Participants who report consuming an average of >3 alcoholic drinks per day in the 30 days prior to study enrollment
    6. Participants with any past or current diagnosis of schizophrenia, narcolepsy, heart disease, epilepsy, or a traumatic brain injury
    7. Participants who are currently experiencing untreated bipolar disorder, major depression, sleep apnea, or other uncontrolled medical conditions as determined by the investigators (e.g., hypertension)
    8. Participants with a known balance or gait disorder
    9. Participants with color blindness (Phase 2 only)
    10. Participants who currently wear hard contact lenses for vision correction (Phase 2 only)
    11. Participants who have donated 450 mL or more of blood in the two weeks prior to study enrollment
    12. Participants who are pregnant or breastfeeding (female participants only)
    13. Participants who report never using cannabis before in their lifetime (Phases 1 & 2 only)
    14. Participants with a history of clinically significant adverse event(s) associated with cannabis intoxication (e.g., lightheadedness, nausea, dizziness, etc., cannabis use groups only)
    15. Participants with uncorrected visual acuity disorder, defined as binocular vision worse than 20/40 (Phases 2, 3 & 4 only; determined at screening)
    16. Participants with a body mass index >40 kg/m2 (determined at screening)
    17. Participants with a positive breath alcohol test (breathalyzer) at screening
    18. Participants who are otherwise unsuitable for inclusion in the study, based on the opinion of the investigator

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Non-Users
People who do not use cannabis.
Daily Flower Users
People who use cannabis flower daily.
Daily Concentrate Users
People who use cannabis concentrate products daily.
Occasional Flower Users
People who use cannabis flower at least once a month and no more than three times per week.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Driving Impairment
Time Frame: 5 years
SDLP (standard deviation of lateral position) is measured by our Advanced NADS minisim
5 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 20, 2020

Primary Completion (Actual)

September 14, 2024

Study Completion (Actual)

September 14, 2024

Study Registration Dates

First Submitted

July 21, 2023

First Submitted That Met QC Criteria

February 5, 2024

First Posted (Actual)

February 12, 2024

Study Record Updates

Last Update Posted (Actual)

April 23, 2026

Last Update Submitted That Met QC Criteria

April 20, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • ColoradoSPH

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Cannabis Use

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