Research agenda
Psilocybin mushrooms
Fungus · natural
What's already known: Read the book
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Unlike programs focused on illness, Metanoia explores natural psychedelics for personal growth in healthy adults: integrating six disciplines for a 360° understanding of whether and how they affect creativity, cognition, and emotional resilience.
Multidisciplinary Research
One question runs through all of them: how do we thrive?
How psychedelics change brain activity, neuroplasticity, and cognition, and what that means for creativity, focus, and emotional resilience in healthy adults.
Read the full research focusCloseStudying natural sources, mushrooms, cacti, vines, and bark, as whole chemical systems, not single molecules. Each carries an "entourage" of related compounds that may shape the experience.
Read the full research focusCloseExploring whether genetic factors influence how individuals respond to psychedelics. Understanding that variation is a precondition for any future standard for growth.
Read the full research focusCloseDeveloping evidence-based frameworks for preparation, the experience itself, and integration, including the role of set, setting, and meditation.
Read the full research focusCloseHow growing conditions, species, and strain shape a source's real chemistry, the variation that makes reproducible research possible or impossible.
Read the full research focusCloseHow sex and gender shape psychedelic response, one of the least-studied questions in the field.
Read the full research focusCloseResearch Focus
Six disciplines, pointed at twelve dimensions of human potential. These are the outcomes our research sets out to understand, and measure. All twelve dimensions now have a published evidence review, with the sources listed on each page.
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Expanding human consciousness, studied rigorously, shared openly.
The Measurement Problem
The dimensions above are what our research sets out to understand. There is an awkward problem with that: we have not identified a common instrument that measures them together over time. This is the least glamorous gap in psychedelic science, and we think it is the most important one.
Background reading: Psychedelics and human development.
A 2024 systematic review in the Journal of Psychopharmacology examined 93 clinical trials of classic psychedelics and found 17 different rating scales in use across them. Its authors called for the field to develop a core outcome set, a common minimum that every study reports, and recommended that instruments be designed to assess the setting of an experience. We have not identified either in use.
There is a second gap underneath the first. Nearly every validated instrument in the field measures the acute experience: what happened during the hours the substance was active. Very little measures what a person was actually seeking, or whether they found it, a month or a year later. For a field increasingly asked to justify itself with durable outcomes, that is a strange place to be.
The consequence shows up plainly in the research. In what its authors describe as the largest prospective study of naturalistic psilocybin use published to date, participants most often named self-exploration, and most named several reasons at once, mental health and therapy among them. Their outcomes were reported on measures of anxiety, depression, alcohol misuse, cognitive flexibility, emotion regulation, spiritual wellbeing, extraversion, neuroticism, and burnout. The purpose a person recorded and the instrument that measured the outcome came from different frames. That same study found that, of those who completed each follow-up, 11% at two to four weeks and 7% at two to three months reported persisting negative effects, and we have not identified a standard for how such an effect should be defined, timed, or recorded.
So results cannot be pooled across studies, benefits cannot be compared, and harms cannot be counted properly. Every new dataset arrives in its own dialect.
Three pieces, all of them plumbing rather than headline science:
All of it will be published openly and free of charge, with no licence fee and no restriction on use, for researchers, state programmes, registries, and clinicians to adopt or adapt. The first piece is out: version 1.1 of the minimum common data element set, 23 elements in six groups with a proposed case definition for persisting adverse effects, is open for public comment until 2 December 2026. The outcome measure is still in development.
Public Comment
On September 22, 2026, Metanoia submitted a written comment to the U.S. Food and Drug Administration in docket FDA-2026-N-7542, its public proceeding on psychedelic drugs. On September 14 we spoke at the agency's public hearing. Metanoia was among the speakers randomly selected from the requests received.
Federal funding is about to reach state psychedelic programs, and we asked the FDA to settle what every record should contain before those databases are built.
Two figures in the spoken remarks came out wrong on the day. The therapy figure should read 47.9 percent, not 78 percent. The executive order is number 14401, not 1441. Both are marked in the transcript below, and our written comment corrects the therapy figure in note 1.
Good afternoon. My name is Shraga Israel, founder of Metanoia, a California nonprofit public charity that conducts research and public education on natural psychedelics in healthy adults. We have no financial relationships with any company in this field. On topic four, I'm asking for one thing, agreed on common data elements before the databases are built, not after. Executive Order 1441 [Correction: the order is Executive Order 14401, Accelerating Medical Treatments for Serious Mental Illness, 91 Federal Register 21709.] directs at least $50 million towards state psychedelics programs, including data sharing. Elements agreed now cost almost nothing. Some can never be added later because they had to be recorded before the person took the drug. The reason for use is the clearest case. A survey of real world psilocybin use asked about 1,800 people why they were taking it before they did. 81% replied self exploration. 71% replied mental health. 78% replied therapy. [Correction: the figure for therapy is 47.9 percent, not 78 percent. Source: Nayak et al., Frontiers in Psychiatry, 2023, survey 3, n = 1,802.] The same people, several reasons each. Non-medical records have no indication field. So databases that reads an empty field as non-medical get most of these people wrong. So we recommend two fields. One, was a condition clinically diagnosed. Two, the person's own reason, more than one if needed, with the date they were recorded. Metanoia is drafting these elements and an outcome instrument built around the reason for use and will publish both openly free of charge. My request is simple. Make data that can be compared a design requirement from day one, not a repair job after data exist. Thank you.
A word on what this is not. We are not claiming to be an authority, and a measure is not made legitimate by being announced. It earns its place by being used, tested, and criticised until either it survives or something better replaces it. So we publish drafts rather than verdicts, we invite people to take them apart, and we will say plainly where we got it wrong. Metanoia is well suited to this particular job for one structural reason: we sell nothing to the people our research informs, so no finding is worth more to us than any other.
The Family We Study
Metanoia did not start with mushrooms and move on to the rest. We started with the classic psychedelics as a family, six natural sources and two synthetics studied for a complete picture, and psilocybin is simply the one with the most work behind it so far. Each brief below is our open question for that substance, not a verdict on it.
These eight cards are research briefs: what remains open, what others are studying now, what Metanoia will ask, and why. For what is already established and readable today, see Education, where the same eight substances live as books that keep updating, one link per card below.
Research agenda
Fungus · natural
What's already known: Read the book
See the full research briefResearch agenda
Tryptamine · natural
What's already known: Read the book
See the full research briefResearch agenda
Vine and leaf brew · natural
What's already known: Read the book
See the full research briefResearch agenda
Cactus · natural
What's already known: Read the book
See the full research briefResearch agenda
Root bark · natural
What's already known: Read the book
See the full research briefResearch agenda
Plant and toad-derived · natural
What's already known: Read the book
See the full research briefResearch agenda
Classic synthetic, covered for a complete picture
What's already known: Read the book
See the full research briefResearch agenda
Classic synthetic · empathogen, covered for a complete picture
What's already known: Read the book
See the full research briefOngoing Projects
Four initiatives that turn scattered global knowledge into something people can actually use.
A continuously updated, science-based library of psychedelic research results: drawn only from trusted, verified sources, and searchable by anyone.
Read moreOngoing Project
The science of psychedelics is scattered, across journals, languages, preprints, and paywalls, and most of it never reaches the people who could use it. We are building a single, continuously updated library that gathers verified research results into one place, searchable by anyone, free of charge.
The discipline is strict: every entry is drawn only from trusted, verified sources, with the link and the claim checked to match. Nothing fabricated, nothing exaggerated. Where the evidence is strong we say so, where it is thin or contested, we say that too, because an honest map of what we don't yet know is as valuable as a map of what we do.
This is core to Metanoia's mission: turning complex, fragmented research into knowledge people can actually understand and act on.
A plain-language, dated summary of what current research says about risks, interactions, and contraindications.
Read moreOngoing Project
Reliable, non-judgmental information about the safe and responsible use of psychedelics is scattered and often drowned out by hype or fear. We are building a written digest that summarizes, in plain language, what current verified research says about interactions, contraindications, and set and setting, with every claim sourced and dated.
It is designed around harm reduction and honesty, not promotion. It will flag real risks clearly: the danger of combining psychedelics with certain antidepressants or MAO-inhibitors, the contraindication for those with a personal or family history of psychosis.
A firm boundary: this is education. It is not a supply service, it does not give personal answers about anyone's use, and it is not a substitute for medical advice.
A global system for collecting, analyzing, and learning from lived psychedelic experiences, historical and ongoing.
Read moreOngoing Project
For decades, people have written careful, first-hand accounts of their psychedelic experiences, a vast, largely untapped record of what these substances actually do in real lives, across cultures and eras. We are building a system to collect, structure, and learn from that record, historical and ongoing.
Lived experience is not a substitute for controlled science, and we never treat it as one. But at scale, and analyzed carefully, it can surface patterns worth studying: which settings tend toward difficulty, how different species or doses are described, how integration shapes lasting outcomes. It is the qualitative counterpart to the research database.
Collected with consent and privacy at the center, this becomes a bridge between the anecdotal and the rigorous.
A common data element set and an outcome measure anchored to purpose, so that results from different studies, programmes, and registries can finally be compared.
Read moreOngoing Project
A 2024 review of 93 clinical trials found 17 different rating scales in use, and its authors called for a core outcome set. We have not identified one in use. Almost every validated instrument in the field measures the acute experience rather than the durable outcome, and we have not identified one designed around what a person was actually seeking. The result is that studies cannot be pooled, benefits cannot be compared, and harms cannot be counted properly.
We are drafting three pieces of plumbing: a minimum common data element set for any record of a psychedelic experience. An outcome measure built on our twelve dimensions and anchored to the purpose a person records before the experience rather than recalls after it, and a standard case definition, with fixed observation windows, for persisting adverse effects.
All of it will be published openly and free, with no licence fee and no restriction on use. We submitted this work to the U.S. Food and Drug Administration as a written comment on September 22, 2026.
We are not claiming to be an authority. A measure earns its place by being used and criticised, not announced, so we publish drafts, invite people to take them apart, and say where we got it wrong.
One Mechanism, Seven Substances
Mesoamerican mushroom cults, the Bwiti of Gabon, the ayahuasqueros of the Amazon, the peyote traditions of North America, and, a century later, a Swiss chemist synthesizing a new molecule, arrived at the same door from completely different directions. What they found, without knowing it, was one receptor.
Every substance on the ring above is, chemically, a match or a near-match for serotonin at one receptor, 5-HT2A, on cells across the brain. Block that receptor and the classic psychedelic effect does not happen. That is the field's actual consensus, not a metaphor about interconnection: an international body of pharmacology, going back decades, agrees that classic psychedelics are agonists or partial agonists at 5-HT2A. Traditions that never had contact with one another built rituals around plants and fungi that all, it turns out, do this one thing.
MDMA sits outside the ring on purpose. It is a member of Metanoia's research family, but it works mainly by releasing the brain's own serotonin rather than mimicking it at this receptor, a different mechanism entirely. We show that honestly rather than force it into a tidier picture.
Shared 5-HT2A mechanism: Nichols DE, "Psychedelics," Pharmacol Rev 68(2):264-355, April 2016 · PMID 26841800 · DOI 10.1124/pr.115.011478. According to PubMed. Presented as education, not medical advice, and not a claim that any tradition's use was safe or legal in every setting.
All Metanoia research follows applicable laws and ethical guidelines, with advisory oversight and clear approval processes. We're transparent about our methods and our limits, especially given the sensitive nature of this field. Metanoia conducts and shares research and education. We do not supply controlled substances.