Skip to main content
OpenTrials
Completed

NCT Number: NCT05160220

Naturalistic Study of Microdosing With Psilocybin

This study seeks to understand the neural, cognitive and behavioral effects of low doses of psilocybin administered in the form of dried mushroom material (0.5 g of Psilocybe cubensis) consumed in natural settings following a placebo-controlled double-blind experimental design.

Completed

Looking for future studies?

Notify Me

Key information

Age range

21 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Instituto de Fisica de Buenos Aires (IFIBA)

Buenos Aires, 1428, Argentina

About this study

Sub-threshold doses of serotonergic psychedelics are frequently consumed as cognitive enhancers, and due to their purported positive effects on mood, energy and creativity ("microdosing").

The acute and short-term effects of psilocybin (the psychoactive compound of Psilocybe cubensis mushrooms) on several variables will be investigated, comprising spontaneous and evoked electrophysiological brain activity, perception and cognitive function (cognitive flexibility, attention, inhibitory control, conscious access, visual perception), creativity (problem solving, divergent and convergent thinking), behavior (actigraphy and sleep patterns, natural language production) and several domains related to well-being and mental health of the participants.

This study is simultaneously naturalistic (i.e. recruited subjects are intrinsically motivated to microdose, as they have decided to embark in a microdosing protocol) and controlled by expectations, following a double-blind placebo-controlled design. Participants will microdose according to the following schedule:

Two sessions (0.5 g dried Psilocybin mushrooms vs. dried edible mushroom material without psychoactive effects as a placebo condition) will be conducted. A third party will be in charge of generating their active dose and placebo capsules, and they will also implement a blinding procedure.

Each session will span one week of measurements. Subjects will be given a smartwatch to monitor activity and sleeping patterns at the beginning of the week. At days 3 and 5, subjects will take capsules with active mushroom material or placebo, and then several variables will be recorded. Experiments will be conducted in a setting that is natural and comfortable for the participants, e.g. their homes.

The main outcome measures consist of resting state activity recorded with EEG, evoked response potentials and performance during cognitive tasks, behavioral variables obtained with actigraphy and automated sleep scoring, natural language analysis, and several measurs self-reported via standarized questionnaires.

After completion, this study will provide direct evidence concerning the efficacy of microdosing for cognitive enhancement under natural conditions, i.e. those most frequently used by individuals who microdose, as well as provide information concerning the potential underlying neurobiological mechanisms.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Men and woman with more than 21 years.
  • Participans are planning to microdose using their own dried mushroom material and adhere to the experimental protocol.
  • No active psychiatric conditions requiring treatment with psychotropic medications.
  • Able to provide informed consent.

Excusion Criteria:

  • Use of psychotropic medication during the study, including stimulants such as caffeine.
  • Prior adverse reactions to psychedelics according to the Challenging Experiences Questionnaire administered during initial screening.
  • Pregnant women or women during lactation
  • History of high or low blood pressure or other cardiovascular risks.

Treatment and study plan

Psilocybin

Drug

0.5 g dried Psilocybe cubensis mushroom material, 0.8 mg psilocybin.

Placebo

Drug

0.5 g dried edible non-psychoactive mushroom material.

Primary outcomes

  1. Resting state oscillations measured with EEG

    Time frame: 1 week

    Our goal is to study changes in spectral content before and during the acute effects with the purpose of comparing changes with those observed under higher doses of psilocybin.

  2. Attention

    Time frame: 1 week

    Measured performance in the attentional blink paradigm

  3. Inhibitory control

    Time frame: 1 week

    Measured using the go/no go experimental paradigm

  4. Conscious access

    Time frame: 1 week

    Measured using the backward masking paradigm

  5. Visual perception

    Time frame: 1 week

    Measured using the binocular rivalry paradigm

  6. Physical activity

    Time frame: 1 week

    Measured using wrist actigraphy using a smartwach

  7. Divergent thinking

    Time frame: 1 week

    Measured using the Alternative Uses Task (AUT)

  8. Attention

    Time frame: 1 week

    Measured using the hiearchical mismatch negativity paradigm combined with EEG

  9. Cognitive flexibility

    Time frame: 1 week

    Measured using the stroop task

  10. Convergent thinking

    Time frame: 1 week

    Measured using the Remote Associations Task (RAT)

  11. Convergent thinking

    Time frame: 1 week

    Measured using the Wallach-Kogan test (WK)

Secondary outcomes

  1. Effect positive/negative affect and well-being

    Time frame: 1 week

    Measured using the Positive and Negative Affect Schedule (PANAS)

  2. Effects on anxiety

    Time frame: 1 week

    Measured using State Trait Anxiety Inventory (STAI)

  3. Effects on personality

    Time frame: 1 week

    Measured using the Big Five inventory (BFI)

  4. Concentration of psilocybin in the dried material

    Time frame: 1 week

    To be measured using high performance liquid chromatography

Sponsors and collaborators

Lead sponsor

National Council of Scientific and Technical Research, Argentina

Other Gov

Registry information

Official study title

Double-blind Placebo-controlled Naturalistic Study of Microdosing With Psilocybin: Effects on Brain Activity, Behavior, Cognition, Creativity, and Mental Health

Acronym: NATMICRO

Important dates

Study start
2021
Primary completion
2021
Study completion
2021
First posted
Dec 16, 2021
Registry last updated
Dec 16, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.