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 — DRUGCannabidiol (CBD) Oil 300mg, 1 dose
- Cannabidiol (CBD) Oil 150mg — DRUGCannabidiol (CBD) Oil 150mg, 1 dose
- Placebo Oil — DRUGPlacebo 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 300mgCannabidiol (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 150mgCannabidiol (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 OilPlacebo 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
- Toni M Rudisill, PhD3042930687
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| West Virginia University | Morgantown | West Virginia | 26506 | Toni M Rudisill, PhD (PRINCIPAL_INVESTIGATOR) |
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