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Examining the neuromodulatory effects of cannabidiol in healthy adults

Examining the neuromodulatory effects of cannabidiol in healthy adults: A randomised, double-blind, placebo-controlled, cross-over trial

Status
Not yet recruiting
Phases
Phase 4
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12626000609358
Acronym
CBD-EEG
Enrollment
40
Registered
2026-05-18
Start date
2026-06-01
Completion date
2026-11-30
Last updated
2026-06-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

This project will be the first to comprehensively test the hypothesis that oral administration of cannabidiol (CBD) oil modulates brain excitation-inhibition (E-I) using a range of electrophysiological measures (aperiodic activity, gamma band oscillatory activity, mismatch negativity) using electroencephalography (EEG) in neurotypical adults. To that end, we will conduct a randomised, double-blind, placebo-controlled, crossover trial to examine the effect of acute dose 600mg CBD oil on EEG-derived measures of brain E-I.

Interventions

- 600mg cannabidiol (CBD) suspended in 6ml of medium-chain triglyceride (MCT) oil plus flavouring. - Single dose, administered oralorally (oil held under tongue for 1 minute). - Adherence will be monitored by trial staff observing participants hold the oil in their mouth for 1 minute (timed by trial staff) before swallowing. - 2-week washout between active and placebo interventions.

Sponsors

Deakin University
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Crossover
Primary purpose
Educational / counselling / training
Masking
Blinded (masking used) (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

• Age 18-40 years • Male or female • Fluent in written and spoken English • Normal or corrected-to-normal vision • Normal hearing • No intellectual disability • Willing to undergo urine and blood sample collection

Exclusion criteria

• Known hypersensitivity to CBD, THC, cannabis or excipients used in product manufacture (MCT oil) • Medicinal cannabis (on prescription) or illicit cannabis use (including unregulated CBD products) in the past 6 months • Pregnant, breastfeeding or planning to become pregnant during the trial • Current psychiatric, developmental, substance use, genetic, and neurological conditions • Intellectual disability • Currently taking psychoactive medications (e.g., benzodiazepines)

Outcome results

None listed

Source: ANZCTR · Data processed: Jun 11, 2026