The Effect of Cannabidiol in Learning and Memory of Adults

NCT ID: NCT06074172

Last Updated: 2025-03-24

Study Results

Results available

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE2

Total Enrollment

57 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-03-14

Study Completion Date

2020-11-06

Brief Summary

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The main objectives of this study were to test if a singular dose of Cannabidiol (1) enhances the learning and memory of healthy human subjects, (2) test if Cannabidiol has negative effects on Retroactive and Proactive Interference during learning, (3) and test if demographic factors will influence CBD's modulation of human learning and memory.

Detailed Description

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Using a randomized, double-blind, placebo-controlled two-arm case-crossover trial, this study investigates the effect of 246 milligrams (mg) of Cannabidiol (CBD) on the learning and memory scores of human subjects, as well as the effect of Cannabidiol on Proactive and Retroactive Interference. This study also investigated the influence of demographic factors on CBD's modulation of human learning and memory.

This study was conducted at Colorado State University-Pueblo (CSU Pueblo) with volunteers recruited from CSU Pueblo and the local Pueblo community. Fifty-seven subjects were randomized in a double-blind manner to receive either CBD or placebo before completing two versions of learning and memory assessments. Each version of the learning and memory assessment included the Montreal Cognitive Assessment (MOCA), the Rey Auditory Verbal Learning Task-Revised (RAVLT-R), and the Logical Memory Subject of the Weschler Memory Scale. Several components of the RAVLT-R were evaluated including the Sum of Trials (Trials I-V) score, Proactive Interference Ratio (PI Ratio), and Retroactive Interference (RI Ratio).

Conditions

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Memory

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Two-arm Case-Crossover
Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Caregivers Outcome Assessors
Triple (Participant, Care Provider, Outcomes Assessor)

Study Groups

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Placebo, Then Cannabidiol

Participants first received a Placebo 246 mg press pill during visit 1. After a washout period of 1 week, subjects received a Cannabidiol press pill during visit 2.

Group Type PLACEBO_COMPARATOR

Placebo (246mg press pill)

Intervention Type DRUG

Placebo press pills were provided by Steve Goods CBD (Longmont, Colorado). Placebo pills were tested by the chemistry lab at CSU Pueblo and by Botanacar in Denver, CO. Both laboratories determined placebo pills to be pure with no heavy metals, bacteria, and pesticides detected.

Cannabidiol, Then Placebo

Participants first received a Cannabidiol 246 mg press pill during visit 1. After a washout period of 1 week, subjects received a Placebo press pill during visit 2.

Group Type ACTIVE_COMPARATOR

Cannabidiol (246mg press pill)

Intervention Type DRUG

Cannabidiol press pills provided by Steve Goods CBD (Longmont, Colorado). CBD pills were tested by the chemistry lab at CSU Pueblo and by Botanacor in Denver, CO. Both laboratories determined CBD pills to be 99.98% pure with no THC, heavy metals, bacteria, and pesticides detected.

Interventions

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Cannabidiol (246mg press pill)

Cannabidiol press pills provided by Steve Goods CBD (Longmont, Colorado). CBD pills were tested by the chemistry lab at CSU Pueblo and by Botanacor in Denver, CO. Both laboratories determined CBD pills to be 99.98% pure with no THC, heavy metals, bacteria, and pesticides detected.

Intervention Type DRUG

Placebo (246mg press pill)

Placebo press pills were provided by Steve Goods CBD (Longmont, Colorado). Placebo pills were tested by the chemistry lab at CSU Pueblo and by Botanacar in Denver, CO. Both laboratories determined placebo pills to be pure with no heavy metals, bacteria, and pesticides detected.

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Were 18 years of age or older

Exclusion Criteria

* Were pregnant or breast-feeding
* Had been diagnosed with mental illness
* Didn't speak English fluently
* Had severe hearing problems
* Had recreational or opioid drug contaminants in their urine
* Were involved in criminal activity
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Institute of Cannabis Research

UNKNOWN

Sponsor Role collaborator

Colorado State University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Moussa M Diawara, PhD

Role: PRINCIPAL_INVESTIGATOR

Colorado State University-Pueblo

Locations

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Colorado State University Pueblo

Pueblo, Colorado, United States

Site Status

Countries

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United States

References

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Gebregzi HH, Zeiger JS, Smith JP, Stuyt L, Cullen L, Carsella J, Rogers DC, Lafebre J, Knalfec J, Vargas A, Diawara MM. Oral cannabidiol did not impair learning and memory in healthy adults. J Cannabis Res. 2025 Jan 23;7(1):5. doi: 10.1186/s42238-025-00262-2.

Reference Type DERIVED
PMID: 39849639 (View on PubMed)

Provided Documents

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Document Type: Study Protocol and Statistical Analysis Plan

View Document

Other Identifiers

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MD012420BM

Identifier Type: -

Identifier Source: org_study_id

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