Not a condition: how psychedelics relate to personality, both as something they may change and as a predictor of the response

Personality & Trait Factors

One of the most repeated claims about psychedelics is that they change who you are: that a single experience can durably raise "openness" and reshape personality. It is a powerful story, and it is shakier than its reputation. The honest version is more modest and more interesting. The trait that most reliably shifts in controlled trials is not openness but neuroticism, which falls, and that overlaps heavily with simply feeling better. Openness changes are often small, sometimes no greater than under a standard antidepressant, and rarely shown to last. The largest "openness" figures come from comparing people who already chose to take psychedelics with people who did not. This page separates the genuine signal (modest, mostly in patients, easy to confuse with symptom relief) from the myth, and notes that personality may matter more as a predictor of the experience than as something the drug rewrites.

Data updated

Key Insights

  • 1

    This is a theme page about personality, not a condition or a treatment. It covers two questions: do psychedelics change personality traits (the famous "openness" claim), and do personality traits predict who responds and how they experience the drug?

  • 2

    The famous claim is weaker than its reputation. In controlled trials the trait that most reliably moves is neuroticism, which falls, not openness. And reduced neuroticism overlaps so much with feeling less depressed or anxious that it may not be independent personality change at all.

  • 3

    Where openness does rise, it is often not specific to the psychedelic. In a head-to-head trial, openness increased just as much under a standard antidepressant, with no difference between the two, and the change was not shown to persist at six months.

  • 4

    The biggest "openness" numbers are not change at all. The largest effects come from cross-sectional surveys comparing people who already use psychedelics with people who do not, which mostly shows that open people are drawn to these drugs, not that the drugs made them open.

  • 5

    Personality may matter more as a predictor than as an outcome. Traits like absorption and suggestibility appear to predict the acute experience and even the response more steadily than personality is shown to change, and a large meta-analysis found no significant effect on most personality measures.

By the numbers

6
Trials tracked

as of July 2026

149
Papers tracked

as of July 2026

1,148
Trial participants

as of July 2026

Research Landscape

What the 6 registered trials connected to Personality & Trait Factors look like when you line them up. Counts come from Blossom’s trial records as of July 2026.

What's live right now, and what stopped?

Sourced

Registry status of all 6 Personality & Trait Factors trials Blossom tracks. Orange marks trials recruiting or opening.

Underway, not recruiting
117%
Completed
467%
Unknown / other
117%

Don't read stopped trials as failures: trials end early for funding, recruitment, and strategy reasons too. Status is as last synced from the registry; some 'recruiting' trials may already have finished.

About Personality & Trait Factors

Personality and trait factors is not a condition or a treatment; it is a theme that runs through the whole field, and it points in two directions. The first is whether psychedelics change personality, the widely repeated idea that these experiences can durably alter stable traits, most famously by increasing "openness to experience". The second, quieter direction is whether personality predicts the response: whether traits a person already has shape how intense their experience is and whether they benefit.

The first question is the glamorous one, and it deserves scepticism precisely because it is so appealing. Personality is, almost by definition, the part of us that is stable over time, so "a single dose durably changed my personality" is an extraordinary claim that calls for strong evidence. The reality in the research is more cautious than the popular telling: the changes are generally modest, concentrated in people being treated for a condition, often not specific to the drug, and rarely demonstrated to last.

The single most important idea to carry through this page is the difference between feeling different and being different. Much of what looks like personality change is hard to separate from simply feeling better: when depression or anxiety lifts, scores on traits like neuroticism fall too, which may be symptom relief wearing the costume of trait change. The steadier, less heralded finding is that personality works as a predictor of the experience, which is a more defensible claim than the headline one. This page is distinct from the clinical personality disorders page, which covers personality as pathology rather than as a dimension that shifts.

Approach & Methods

Because there is no condition here, the relevant "standard practice" is how trait change is measured and how trustworthy those measurements are. The workhorse is the self-report Big Five questionnaire (openness, conscientiousness, extraversion, agreeableness, neuroticism), administered before and after. The best controlled evidence comes from layering these scales onto efficacy trials: a psilocybin trial for alcohol use disorder found reduced neuroticism and raised extraversion and openness against placebo[1], which is a genuine, placebo-controlled signal. But the cleanest comparison is sobering: in a head-to-head against escitalopram, openness rose under both the psilocybin and the antidepressant, with no difference between them, and only neuroticism stayed reduced at six months[2].

Two measurement problems sit underneath all of this. First, short-window self-report struggles to distinguish a real trait shift from a lingering good mood, so a "personality change" measured weeks after a transformative experience may partly be state, not trait. Second, durability is rarely tested: most studies stop well before the months or years it would take to show a trait has genuinely, stably moved. The honest summary is that the measurement tools are adequate for symptoms but stretched when asked to prove that something as stable as personality has been rewritten, and the strongest single review across this literature is largely null[3].

Independent Research

Exploratory Research Report

This report summarises what Blossom’s database shows about psychedelics and personality. It is worth being clear what kind of page this is. It is not a condition page and not a treatment. It is about a famous idea, that psychedelics can change personality, and a quieter one, that personality shapes the response, and about how much weight the evidence can actually bear. The short answer is that the famous idea is more myth than the field admits, and the quiet idea is the steadier one.

A note before the evidence

This page is a research summary, not medical advice, and nothing here is a recommendation to take psychedelics. It is also worth a specific caution: claims that a single experience will durably improve your personality are exactly the kind of appealing, hard-to-test promise that this literature does not support. Read the evidence below as a corrective to that promise, not an endorsement of it.

The famous claim, and why it is shaky

The headline is that psychedelics durably increase "openness to experience", one of the Big Five personality traits. It is repeated everywhere, and it is weaker than it sounds. The most revealing evidence is a head-to-head trial: in psilocybin versus escitalopram for depression, openness rose under both, with no significant difference between the psychedelic and the ordinary antidepressant, and the change was not shown to persist to six months[1]. If a standard antidepressant moves "openness" just as much, the trait shift is not a special property of the psychedelic experience.

There is a genuine controlled signal, but it points elsewhere. A psilocybin trial in alcohol use disorder found reduced neuroticism and increased extraversion and openness against placebo[2], and a healthy-volunteer study found reduced neuroticism a month after a high dose[3]. Notice the pattern: the trait that moves most reliably is neuroticism, downward. And reduced neuroticism is very hard to separate from simply being less depressed and anxious, which is to say it may be symptom relief showing up on a personality scale, not personality change as such.

The numbers that look biggest are not change at all

The most dramatic "openness" figures come from a different kind of study entirely. A large cross-sectional survey found a very large openness difference (d=1.72) between people who use psychedelics and people who do not[4]. That sounds like overwhelming evidence until you notice it is not a before-and-after at all: it compares two different groups of people at one moment. The straightforward explanation is self-selection, open, curious, experience-seeking people are more likely to take psychedelics in the first place. The drug did not necessarily make them open; their openness helped lead them to the drug.

This is the single most common error in the personality story, and it is worth stating plainly: a difference between users and non-users is not evidence that the drug changed anyone. The honest, within-person, controlled evidence is far more modest than the cross-sectional gap implies, and the broadest synthesis of it, a meta-analysis of ten studies and 304 participants, found no significant effect on the majority of personality and related measures[5]. That null result is the proper baseline against which every exciting individual finding should be read.

Personality as a predictor: the steadier story

There is a version of this topic that holds up better, and it is the one that gets less attention. Rather than asking whether psychedelics change personality, it asks whether personality predicts the experience and the response. Here the evidence is steadier. Traits like absorption and suggestibility appear to forecast outcomes: pre-treatment suggestibility predicted response to psilocybin (but not to escitalopram)[6], and personality measurably shapes the sensory character of the experience[7] and predicts features of the LSD state[8]. This is more useful and more defensible than the trait-change claim, because it does not require personality to do the one thing personality is defined not to do, change easily.

Interestingly, the same work complicates the lazy "it is all expectancy" dismissal. In one trial, expectancy for psilocybin did not predict the response to psilocybin[6], so the changes are not simply a matter of believing the drug will work. The picture is subtler than either "psychedelics transform personality" or "it is all placebo": specific traits predict specific responses, in ways that are starting to be mapped, even as durable trait change remains unproven.

Why "personality change" is an extraordinary claim

It helps to remember what personality is. By definition, traits are the relatively stable, enduring patterns that persist across situations and years, which is exactly why "a single dose durably changed my personality" demands strong evidence. The field has small samples, self-report questionnaires administered over weeks rather than years, few long follow-ups, and effects that are often non-specific or null. The naturalistic reports of lasting change, such as ayahuasca cohorts describing durable personality and quality-of-life shifts[9], are uncontrolled and self-selected, and the survey work on perceived personality change[10] measures belief about change, not change itself.

None of this means nothing happens. People plainly have experiences they describe as changing them, and in patients some trait scores do move under controlled conditions. The defensible claim is narrow: that easing an illness can shift some trait measures, mostly neuroticism downward, in ways that may reflect symptom relief and may or may not last. The grand claim, that psychedelics reliably and durably rewrite healthy personality, is not something this evidence establishes.

Reading this honestly

So how should you read the personality story? As a famous claim that needs deflating, paired with a quieter one worth taking seriously. The deflation: "psychedelics durably increase openness" rests on small samples, short follow-ups, effects no larger than a standard antidepressant, cross-sectional comparisons mistaken for change, and a broad meta-analysis that is mostly null. The trait that actually moves in controlled work is neuroticism, downward, and that is hard to distinguish from feeling better. The quieter, sturdier story is that personality predicts the experience and the response, which is both more defensible and more clinically useful. The most valuable thing this literature offers an honest reader is the discipline to ask, every time someone says a psychedelic changed who they are, a simple question: changed compared to what, measured how, and for how long? The answers, so far, are more modest than the myth.

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Acute Effect Characterisation

Psilocybin

This matrix characterises the prominence of each compound’s personality/trait-change signal, not therapeutic efficacy. Psilocybin is the strongest case: placebo-controlled reductions in neuroticism and some rise in openness in patient samples. But the openness change was not specific versus escitalopram, durability past six months is unshown, and the best meta-analysis is largely null. A real but modest signal, easy to confuse with symptom relief.

Medium MagnitudeLow EvidenceModerate Consistency

Published research

45
linked papers
11
clinical papers
3
syntheses

Latest linked paper 2026

Registered research

1 registered trial

0 recruiting/opening

83 combined reported enrollment

Phase not assigned

LSD

Trait-effect characterisation, not efficacy. The LSD evidence is mostly cross-sectional or about predicting the acute experience rather than controlled within-person trait change. Suggestive of context- and personality-dependent effects, but little hard evidence that LSD changes traits.

Small MagnitudeLow EvidenceLow Consistency

Published research

23
linked papers
1
clinical papers
5
syntheses

Latest linked paper 2025

Registered research

0 registered trials

0 recruiting/opening

0 combined reported enrollment

Phase not assigned

MDMA

Trait-effect characterisation, not efficacy. The one placebo-controlled healthy-adult trial found its pre-specified personality hypotheses null, with only a medium-effect openness and affect bump at 48 hours. That is a short-term, state-level change, not demonstrated durable trait change.

Small MagnitudeVery Low EvidenceLow Consistency

Published research

20
linked papers
2
clinical papers
3
syntheses

Latest linked paper 2024

Registered research

2 registered trials

0 recruiting/opening

41 combined reported enrollment

Highest Phase I

Ayahuasca

Trait-effect characterisation, not efficacy. Naturalistic and traditional-setting cohorts report lasting personality and quality-of-life changes, but the evidence is uncontrolled and heavily self-selected, with strong demand characteristics. Evocative, not established.

Small MagnitudeVery Low EvidenceLow Consistency

Published research

24
linked papers
0
clinical papers
1
syntheses

Latest linked paper 2026

Registered research

0 registered trials

0 recruiting/opening

0 combined reported enrollment

Phase not assigned

5-MeO-DMT

Trait-effect characterisation, not efficacy. Almost all 5-MeO-DMT work is early-phase pharmacology and safety, with only retreat-based "psychological change" reports and no proper trait endpoints. The personality evidence is essentially absent.

Small MagnitudeVery Low EvidenceLow Consistency

Published research

4
linked papers
1
clinical papers
0
syntheses

Latest linked paper 2026

Registered research

0 registered trials

0 recruiting/opening

0 combined reported enrollment

Phase not assigned

Matrix record updated 14 Jul 2026

Research Outlook

The more promising research direction is the less glamorous one: personality as a predictor rather than a product. Traits such as absorption and suggestibility appear to forecast the acute experience and even the response, and one trial found that pre-treatment suggestibility predicted response to psilocybin specifically[1], while personality measurably shapes the sensory texture of the experience[2] and predicts features of the LSD state[3]. This is steadier ground than the trait-change claim, and potentially more useful, since predicting who will respond, or who will struggle, has real clinical value.

On the trait-change question itself, the most valuable work will be the kind that is currently missing: adequately powered trials with personality change as a primary outcome and genuinely long follow-up, designed to separate trait shift from symptom relief and from expectancy. The reframing in the alcohol study, which described its findings as a normalisation of abnormal personality expression in patients rather than generic enhancement[4], points the honest way forward. The likely outcome is not the dramatic "psychedelics rewrite who you are" headline, but a narrower, more defensible claim: that in people who are unwell, easing the illness can shift some trait scores, mostly downward on neuroticism, in ways that may or may not prove durable.

Industrial Landscape

The personality story has unusual cultural reach, which shapes who promotes it. The idea that a psychedelic can durably increase openness is attractive to the wellness and retreat industry (it promises lasting self-improvement), to researchers (it is a striking, publishable finding), and to users (it gives a transformative experience a measurable-sounding label). That alignment of incentives is exactly why the claim spreads faster than the evidence, and why a cross-sectional difference between users and non-users gets repeated as if it were proof of change. The same survey-based work that produces the eye-catching openness gap is, on inspection, mostly self-selection[1].

For an honest broker, this is a topic to deflate carefully rather than dismiss. There is a real, modest signal, especially reduced neuroticism in patients, and personality genuinely matters as a predictor of the experience. But "psychedelics change your personality" is an extraordinary claim resting on small samples, self-report scales, short follow-ups, non-specific effects and a founding study that does not even appear in much of the current evidence base. The responsible posture credits the modest, patient-centred findings, treats naturalistic "lasting personality change" reports as hypothesis-generating[2], and resists the slide from "people felt changed" to "their personality was durably altered", a slide the survey literature on perceived change[3] shows is very easy to make.

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Quick Indicators

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Not a condition: how psychedelics relate to personality, both as something they may change and as a predictor of the response
Trials
6
Papers
149

Organisations

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University of Washington

At UW, researchers are working on clinical trials with psilocybin (provided by Usona). Dr Anthony Back, co-director of the University's Center for Excellence in Palliative Care, led a trial exploring the effects of psilocybin to alleviate the mental health burden inflicted on frontline healthcare workers throughout the COVID-19 pandemic. As Seattle became the largest city in the US to decriminalise psilocybin mushrooms in October 2021, and with ongoing legislative efforts at the state level, more research with psychedelics is anticipated and occurring at UW.

University of Basel

The University of Basel Department of Biomedicine hosts the Liechti Lab research group, headed by Matthias Liechti. Research here is primarily focused on the pharmacology of psychoactive substances. Much of the clinical research exploring the effects of LSD is taking place at University Hospital Basel. Researchers here are exploring the potential of LSD to treat Cluster Headache, Major Depressive Disorder and anxiety associated with severe somatic diseases. Professor Liechti is also conducting studies comparing the acute effects of LSD, psilocybin and mescaline, and MDMA for fear extinction.

Maastricht University

While Maastricht University may not have a single dedicated psychedelic research group, various researchers at the university are investigating the effects of psychedelics. Early research exploring psychedelics at Maastricht focused on the dangers of MDMA. Now, research into the effects of microdosing is being led by Dr Kim Kuypers. Other research ongoing at the university is investigating cannabis as well as novel psychoactive substances (NPS). Maastricht is collaborating on research with the Beckley Foundation as well as Silo Pharma.

Psychedelic Data Society

The Psychedelic Data Society is a US-based citizen-science nonprofit managing the Psychedelic Data Project, a global harm reduction and research initiative that collects participant-contributed data to accelerate psychedelic science and inform evidence-based drug policy reform.

Quantified Citizen Technologies Inc.

Quantified Citizen Technologies Inc. is a Canadian privacy-centric mobile health research platform powering decentralized citizen-science studies; it built the world's first mobile app for psychedelic microdosing data collection (Microdose.me) with over 19,000 participants worldwide, whose findings were published in Nature Scientific Reports, and continues to host multiple psychedelic observational studies in partnership with MAPS, UBC, and researchers including Paul Stamets and James Fadiman.

Federico Cavanna

Researcher in psychedelic science / neuroscientific researcher (exact current title not confidently verified)

He is a coauthor on multiple widely cited studies on psilocybin microdosing, DMT, and psychedelic use, helping characterize subjective, behavioral, and cognitive effects of psychedelics.

Robin Murphy

Researcher at the University of Auckland School of Pharmacy

She is a coauthor on multiple human psychedelic studies spanning LSD microdosing, sleep, and psilocybin/escitalopram comparisons, making her part of the team contributing to the modern evidence base for psychedelic medicine.

Jeanine Kamphuis

Psychiatrist and researcher at the Department for Mood Disorders, University Hospital Groningen (UMCG)

She studies ketamine, esketamine, and classic psychedelics for treatment-resistant psychiatric disorders, including depression, and is a coauthor on multiple psychedelic/ketamine reviews and clinical studies.

Henrik Jungaberle

Dr. sc. hum., CEO and founder of the MIND Foundation; Head of Development at OVID Clinic Berlin

He is a prominent European psychedelic research and implementation figure contributing to psilocybin clinical trials, harm reduction, and healthcare integration work.

Aaron Klaiber

Doctoral researcher at the University of Basel

He appears as an author on multiple controlled human psychedelic studies spanning DMT, mescaline, MDMA, LSD, and psilocybin, suggesting a substantial role in contemporary psychopharmacology research.

Joost Breeksema

Postdoctoral researcher and Executive Director of the OPEN Foundation

He is a prominent psychedelic researcher and advocate whose work helps shape evidence-based psychedelic policy, ethics, and patient-centered understanding of psychedelic and ketamine/esketamine treatments.

Juliana Rocha

Doutoranda em Ciências Médicas / Saúde Mental at the Ribeirão Preto Medical School, University of São Paulo

She is a recurring coauthor on clinical psychedelic studies, especially ayahuasca trials on social anxiety, emotion recognition, personality, and social cognition, helping expand the human evidence base for psychedelic-assisted psychiatric research.

Mathieu Seynaeve

Senior Medical Director and Head of Psychotherapy at Beckley Psytech

He is a clinical development leader behind multiple human studies of 5-MeO-DMT and psilocybin, including trials in alcohol use disorder, treatment-resistant depression, and headache disorders.

Michiel Van Elk

Associate Professor of Cognitive Psychology at Leiden University

Michiel van Elk is a prominent psychedelic science researcher known for rigorous, skeptical work on psilocybin, microdosing, expectancy effects, and the psychological mechanisms and risks of psychedelic experiences.

Jolien Veraart

Psychiatrist and PhD researcher at the University Medical Center Groningen / University of Groningen

She is a leading clinical researcher on ketamine and oral esketamine for treatment-resistant depression, including safety, efficacy, and real-world implementation.

Kate Godfrey

Research Associate at Imperial College London’s Centre for Psychedelic Research

Kate Godfrey is notable for contributing to leading human psychedelic research on microdosing, neuroimaging, and neuroplasticity at Imperial College London.

Erich Studerus

Psychologist and Scientific Director at fepsy Basel; Lecturer at FHNW

He is a recurring author on influential human psychedelic studies, especially on psilocybin, LSD, MDMA, and ayahuasca effects and predictors of response.

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