The Effects of Cannabidiol on the Driving Performance of Healthy Adults by Dose and Sex

Part of paid clinical trials in Morgantown, West Virginia.

Sponsor
West Virginia University
Study ID
NCT06686914
Phase
PHASE1
Status
Recruiting

Conditions

  • Cannabidiol Effects
  • Driving Performance

Eligibility Criteria

Sex
ALL
Age
18 Years - 30 Years
Healthy Volunteers
Accepted

Interventions

  • Cannabidiol (CBD) Oil 300mg — DRUG
    Cannabidiol (CBD) Oil 300mg, 1 dose
  • Cannabidiol (CBD) Oil 150mg — DRUG
    Cannabidiol (CBD) Oil 150mg, 1 dose
  • Placebo Oil — DRUG
    Placebo Oil, 1 dose

Study Details

The objectives/purpose of this study are to comprehensively investigate the effects of non-prescription CBD on driving performance, drowsiness, sedation, and cognitive function in a large sample of healthy adults aged 18-30 years, with additional characterization of effects by dose and by sex, using a rigorous RCT design which will naturally mitigate confounding factors.

Key Dates

Start date
Jun 30, 2025
Status verified
Oct 2025
Primary completion
Dec 31, 2028
Completion
May 1, 2029

Study Design

Enrollment
300 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE

Arms

  • Active Comparator: Cannabidiol (CBD) Oil 300mg
    Cannabidiol (CBD) Oil, 300mg, 1 dose, 120 minutes prior to testing. After consumption of the respective treatment drug, the participant will be given a standardized meal and wait for 120 minutes to allow for drug absorption and for CBD to begin taking effect; this time frame was chosen based on the pharmacokinetics of CBD along with the consideration of participant burden (max absorption 2-5 hours; average half-life 17 hours).
  • Active Comparator: Cannabidiol (CBD) Oil 150mg
    Cannabidiol (CBD) Oil, 150mg, 1 dose, 120 minutes prior to testing. After consumption of the respective treatment drug, the participant will be given a standardized meal and wait for 120 minutes to allow for drug absorption and for CBD to begin taking effect; this time frame was chosen based on the pharmacokinetics of CBD along with the consideration of participant burden (max absorption 2-5 hours; average half-life 17 hours).
  • Placebo Comparator: Placebo Oil
    Placebo Oil 1 dose 120 minutes prior to testing. After consumption of the respective treatment drug/placebo, the participant will be given a standardized meal and wait for 120 minutes to allow for drug absorption and for CBD to begin taking effect; this time frame was chosen based on the pharmacokinetics of CBD along with the consideration of participant burden (max absorption 2-5 hours; average half-life 17 hours).

Primary Outcome Measure

Mean standard deviation of lateral position [ Time Frame: 150 minutes post intervention ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
West Virginia UniversityMorgantownWest Virginia26506
Toni M Rudisill, PhD
304-293-0687
Toni M Rudisill, PhD (PRINCIPAL_INVESTIGATOR)

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