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This is a double-blind placebo-controlled study investigating the acute and persisting effects of psilocybin on meditation, spirituality, health, well-being, prosocial attitudes, and brain functioning.
This study will use questionnaires and functional magnetic resonance imaging (fMRI) to examine the acute and persisting effects of psilocybin on brain function, meditation, spirituality, and psychology. The majority of the study procedures -- including screening, preparatory meetings, placebo and psilocybin sessions, and a large battery of behavioral and psychological measures -- will be conducted at the investigator's laboratory at the Behavioral Pharmacology Research Unit (BPRU) on the Johns Hopkins Bayview campus. The brain imaging procedures will be conducted at F.M. Kirby Research Center at the Kennedy Krieger Institute (KKI).
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| One all-day session | Experimental | Participants will complete on all-day study session with a moderately-high dose of psilocybin. Preparation will include two days of screening, and an additional 8 hours of session preparation over at least 2 days. Follow-up will consist of an interview and MRI scan one day after the all-day session, a questionnaire follow-up 2 months after the all-day session, and a final follow-up 12-18 months after the all-day session. |
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| Two all-day sessions | Experimental | Participants will complete two all-day study sessions, the first with placebo and the second with a moderately-high dose of psilocybin. Preparation will include two days of screening and 8 hours of session preparation over at least 2 days, before the first all-day session. Follow-up will consist of an interview and MRI scan one day after each all-day session, a questionnaire follow-up 2 months after each all-day session, and a final follow-up 12-18 months after the second all-day session. |
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| Three all-day sessions | Experimental | Participants will complete three all-day study sessions, the first two with placebo and the third with a moderately-high dose of psilocybin. The majority of participants (over 90%) will be assigned to either one or two all-day sessions. A small minority of participants (less than 10%) will be assigned to three all-day sessions. Preparation will include two days of screening and 8 hours of session preparation over at least 2 days, before the first all-day session. Follow-up will consist of an interview and MRI scan one day after each all-day session, a questionnaire follow-up 2 months after each all-day session, and a final follow-up 12-18 months after the third all-day session. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Moderately-high dose of psilocybin | Drug | Oral dose of a moderately-high dose of psilocybin. |
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| Measure | Description | Time Frame |
|---|---|---|
| Persisting Effects Questionnaire | This is a measure of changes in spirituality, personal well-being, relationships, and emotions. | 2 months and 12-18 months post-session |
| Hood Mysticism Scale | This measures subjective experiences associated with classical mystical experiences. | End of session day. |
| States of Consciousness Questionnaire | Measures subjective experience associated with classical mystical experiences. | End of session day |
| fMRI Resting State Functional Connectivity | Measures change in activity in brain regions that have been previously shown to be modulated by either psilocybin or meditation. | 2 months pre and 1 day post session |
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Inclusion criteria:
Exclusion criteria:
Psychiatric Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Behavioral Pharmacology Research Unit, Johns Hopkins Bayview Medical Center | Baltimore | Maryland | 21224 | United States |
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| ID | Term |
|---|---|
| D007785 | Lactose |
| ID | Term |
|---|---|
| D004187 | Disaccharides |
| D009844 | Oligosaccharides |
| D011134 | Polysaccharides |
| D002241 | Carbohydrates |
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| MRI of the acute effects of psilocybin | Experimental | This is an optional arm consisting of two sessions where either placebo, a very-low dose of psilocybin, or a moderately-low dose of psilocybin will be administered. During each session, participants will undergo MRI scanning shortly after the administration of each dose. Study sessions may occur over one or two days. Participants who have previously completed an all-day session with psilocybin in this study will be eligible to volunteer for this arm. |
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| Moderately-low dose of psilocybin | Drug | Oral dose of a moderately-low dose of psilocybin. |
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| Very-low dose of psilocybin | Drug | Oral dose of a very-low dose of psilocybin. |
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| Placebo | Drug | An oral placebo (lactose pill). |
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| D000073893 |
| Sugars |