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Elucidating the acute effects of medically prescribed oral and vaporised delta-9-tetrahydrocannabinol on cognitive functions important for driving.

Kayla B Stefanidis, Carla Schiemer, Taren Mieran, Andrew Hill, Mark S Horswill, Mathew J Summers

Drug and Alcohol Review May 2025 DOI: 10.1111/dar.14060 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Within-subject experimental study with counterbalanced baseline and post-cannabis sessions Peer reviewed
Sample size 78
Population Medicinal cannabis patients: 41 oral cannabis oil users (Study 1) and 37 cannabis flower users (Study 2)
Dose one dose
Duration Baseline and post-cannabis sessions approximately 1 week apart; cognitive battery 90 min after oral oil or 15 min after vaporised flower
Measures Trail Making Test Part B (TMT B), TMT ratio
Topics Cannabis
Keywords Cognition Delta‐9‐tetrahydrocannabinol Neuropsychology
Key findings Acute cannabis oil or flower use did not change information processing speed, divided or sustained attention, or inhibitory control in medicinal cannabis patients after excluding those with a positive drug indication at session start, which the authors say highlights tolerance. However, TMT B performance dropped significantly, and the TMT ratio fell after cannabis oil, suggesting TMT B may be sensitive to acute cannabis use.

Abstract

This program of research investigated the acute effects of orally ingested (Study 1) and vaporised (Study 2) cannabis containing delta-9-tetrahydrocannabinol (THC) on cognitive functions relevant for driving in two samples of medicinal cannabis patients (Study 1 N = 41 oral users; Study 2 N = 37 flower users). Participants completed counterbalanced baseline (no cannabis) and cannabis consumption (post-cannabis) appointments scheduled approximately 1 week apart. During each session, participants were administered a cognitive battery assessing information processing speed, sustained and divided attention, inhibitory control and mental flexibility. In the post-cannabis condition, the battery was completed 90 min after consuming one dose of cannabis oil (Study 1) or 15 min after vaporising one dose of cannabis flower (Study 2). In both samples, acute cannabis oil and flower administration did not induce a change in information processing speed, divided and sustained attention, or inhibitory control performance (after excluding participants with a positive drug indication at the start of either session), highlighting the moderating role of tolerance. However, significant reductions in TMT B performance were observed. Further, TMT ratio was significantly reduced post consumption of cannabis oil. TMT B may be sensitive to acute cannabis consumption in medicinal cannabis patients. However, further research is needed to determine the nature and duration of these effects, and whether such effects vary depending on the population studied (e.g., regular vs. new users).

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Study Year Design Participants
Smoked Cannabis' Psychomotor and Neurocognitive Effects in Occasional and Frequent Smokers Occasional (<2x/week) and frequent (≥4x/week) cannabis smokers 2015 Controlled within-subjects study n = 25
Dissociable effects of cannabis with and without cannabidiol on the human brain’s resting-state functional connectivity Healthy volunteers experienced with cannabis but not regular users 2019 Within-subjects experimental design n = 17
Which biological and self-report measures of cannabis use predict cannabis dependency and acute psychotic-like effects? Young cannabis users 2018 Observational study (naturalistic, within-subject counterbalanced design) n = 410
Cannabis Essential Oil: A Preliminary Study for the Evaluation of the Brain Effects Healthy volunteers 2018 Experimental study n = 5
Coming off cannabis: a cognitive and magnetic resonance imaging study in patients with multiple sclerosis Patients with multiple sclerosis who began using cannabis after disease onset, used it... 2019 Quasi-experimental study with odd-even allocation n = 40

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