- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06255054
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
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Colorado
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Denver, Colorado, United States, 80220
- Driving Study Lab
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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:
- Participants who are ≥21 years old and ≤55 years old
- Participants who are able to provide written, informed consent
- Participants with active healthcare coverage (including health insurance, Medicaid, etc.)
- 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)
- Participants who agree to refrain from using non-prescription psychotropic drugs (e.g., ecstasy), hallucinogens, and synthetic cannabinoids during the study
- 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)
- 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)
- 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)
- 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)
- 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)
- 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:
- Prisoners
- Participants who have nocturnal schedules (e.g., work night shifts)
- Participants with a history of abuse or addiction to substances other than cannabis (e.g., prescription and non-prescription pharmaceuticals, alcohol, or illicit drugs)
- Participants who have expressed an interest in substance abuse treatment within the 60 days prior to study enrollment
- Participants who report consuming an average of >3 alcoholic drinks per day in the 30 days prior to study enrollment
- Participants with any past or current diagnosis of schizophrenia, narcolepsy, heart disease, epilepsy, or a traumatic brain injury
- 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)
- Participants with a known balance or gait disorder
- Participants with color blindness (Phase 2 only)
- Participants who currently wear hard contact lenses for vision correction (Phase 2 only)
- Participants who have donated 450 mL or more of blood in the two weeks prior to study enrollment
- Participants who are pregnant or breastfeeding (female participants only)
- Participants who report never using cannabis before in their lifetime (Phases 1 & 2 only)
- Participants with a history of clinically significant adverse event(s) associated with cannabis intoxication (e.g., lightheadedness, nausea, dizziness, etc., cannabis use groups only)
- Participants with uncorrected visual acuity disorder, defined as binocular vision worse than 20/40 (Phases 2, 3 & 4 only; determined at screening)
- Participants with a body mass index >40 kg/m2 (determined at screening)
- Participants with a positive breath alcohol test (breathalyzer) at screening
- 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 |
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Non-Users
People who do not use cannabis.
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Daily Flower Users
People who use cannabis flower daily.
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Daily Concentrate Users
People who use cannabis concentrate products daily.
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Occasional Flower Users
People who use cannabis flower at least once a month and no more than three times per week.
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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.
Sponsor
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
Keywords
Additional Relevant MeSH Terms
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.
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