Pilot Study: Effects of Psilocybin on Behavior, Psychology and Brain Function in Long-term Meditators

Brief Summary

This is a pilot study to finalize methods for a larger study being planned for the future. This research is being done to characterize performance of tasks, brain functioning, and the effects of psilocybin in individuals with a long-term meditation practice. There are three different parts of the pilot study: 1. Effects of psilocybin on psychological function: This version of the pilot study will involve 1 or 2 day-long psilocybin sessions, and several meetings and data assessment visits. You will make a total of about 5 to 10 visits to our research unit (the BPRU on the Johns Hopkins Bayview Campus). 2. Performance on behavioral and cognitive tasks: This version of the pilot study will involve completing various behavioral and cognitive tasks at our research unit. You will make a total of about 1-10 visits to our research unit (the BPRU on the Johns Hopkins Bayview Campus). 3. Brain functioning: This version of the study will involve 1 to 3 brain imaging (MRI) measurements. You will make a total of about 2 to 5 visits to our research unit (the BPRU on the Johns Hopkins Bayview Campus). The MRI measurements will be taken at the F.M. Kirby Research Center at the Kennedy Krieger Institute (across the street from the Johns Hopkins Hospital). People who are between the ages of 25 and 80 years old, who have a current, regular meditation practice, and who meet the medical requirements may join.

Intervention / Treatment

  • Psilocybin (DRUG)
    dose manipulation as described in the protocol

Condition or Disease

  • Psilocybin
  • Hallucinogens
  • Pharmacologic Actions
  • Central Nervous System Agents
  • Therapeutic Uses
  • Psychotropic Drugs

Phase

  • Phase 1
  • Study Design

    Study type: INTERVENTIONAL
    Status: Completed
    Study results: No Results Available
    Age: 25 Years to 80 Years
    Enrollment: 10 (ESTIMATED)
    Funded by: Other
    Allocation: Non-Randomized
    Primary Purpose: Basic Science

    Masking

    Clinical Trial Dates

    Start date: May 01, 2013
    Primary Completion: Jan 01, 2014 ACTUAL
    Completion Date: May 01, 2014 ACTUAL
    Study First Posted: Nov 20, 2013 ESTIMATED
    Results First Posted: Aug 30, 2020
    Last Updated: May 19, 2014

    Sponsors / Collaborators

    Lead Sponsor: Johns Hopkins University
    Responsible Party: Roland Griffiths

    Participant Groups

    • psilocybin dose manipulation as described in the protocol

    • No description provided

    • No description provided

    Eligibility Criteria

    Sex: All
    Minimum Age: 25
    Maximum Age: 80
    Age Groups: Adult / Older Adult
    Healthy Volunteers: Yes

    Inclusion Criteria:

    * 25 to 80 years old
    * Have given written informed consent
    * Have some college-level education (college degree preferred)
    * Be healthy and psychologically stable as determined by screening for medical and psychiatric problems via a personal interview, a medical questionnaire, a physical examination, an electrocardiogram (ECG), and routine medical blood and urinalysis laboratory tests
    * Agree to consume approximately the same amount of caffeine-containing beverage (e.g., coffee, tea) that he/she consumes on a usual morning, before arriving at the research unit on the mornings of drug session days. If the participant does not routinely consume caffeinated beverages, he/she must agree not to do so on session days.
    * Agree to refrain from using any psychoactive drugs, including alcoholic beverages and nicotine, within 24 hours of each drug administration. The exception is caffeine. Participants will be required to be non-smokers.
    * Agree not to take any PRN medications on the mornings of drug sessions
    * Agree not to take sildenafil (Viagra®), tadalafil, or similar medications within 72 hours of each drug administration.
    * Agree that for one week before each drug session, he/she will refrain from taking any nonprescription medication, nutritional supplement, or herbal supplement except when approved by the study investigators. Exceptions will be evaluated by the study investigators and will include acetaminophen, non-steroidal anti-inflammatory drugs, and common doses of vitamins and minerals.

    Exclusion Criteria:

    * Women who are pregnant (as indicated by a positive urine pregnancy test assessed at intake and before each drug session) or nursing; women who are of child-bearing potential and sexually active who are not practicing an effective means of birth control.
    * Cardiovascular conditions: coronary artery disease, stroke, angina, uncontrolled hypertension, a clinically significant ECG abnormality (e.g., atrial fibrillation), or TIA in the past year
    * Epilepsy with history of seizures
    * Insulin-dependent diabetes; if taking oral hypoglycemic agent, then no history of hypoglycemia
    * Currently taking psychoactive prescription medication on a regular (e.g., daily) basis
    * Currently taking on a regular (e.g., daily) basis any medications having a primary centrally-acting pharmacological effect on serotonin neurons or medications that are MAO inhibitors. For individuals who have intermittent or PRN use of such medications, psilocybin sessions will not be conducted until at least 5 half-lives of the agent have elapsed after the last dose.
    * More than 20% outside the upper or lower range of ideal body weight according to Metropolitan Life height and weight table

    Psychiatric Exclusion Criteria:

    * Current or past history of meeting DSM-IV criteria for Schizophrenia, Psychotic Disorder (unless substance-induced or due to a medical condition), or Bipolar I or II Disorder
    * Current or past history within the last 5 years of meeting DSM-IV criteria for alcohol or drug dependence (excluding caffeine and nicotine) or severe major depression
    * Have a first or second-degree relative with Schizophrenia, Psychotic Disorder (unless substance induced or due to a medical condition), or Bipolar I or II Disorder
    * Has a psychiatric condition judged to be incompatible with establishment of rapport or safe exposure to psilocybin

    fMRI Exclusion Criteria:

    * Head trauma
    * Claustrophobia
    * Cardiac pacemaker
    * Implanted cardiac defibrillator
    * Aneurysm brain clip
    * Inner ear implant
    * Artificial heart valve (last 6 weeks)
    * Prior history as a metal worker and/or certain metallic objects in the body

    Primary Outcomes
    • Measures changes in spirituality, personal well-being, relationships, and emotions.

    • Measures subjective experience associated with classical mystical experiences.

    • Measures subjective experience associated with classical mystical experiences.

    More Details

    NCT Number: NCT01988311
    Other IDs: NA_00047665
    Study URL: https://clinicaltrials.gov/study/NCT01988311
    Last updated: Sep 29, 2023