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Mental health outcomes following a psilocybin session within Oregon’s state-regulated model: A naturalistic study

Amanda Gow, Emily Shih, Ryan Reid, Jimmy J Qian, Charan Mellor, L. Alison Mcinnes, Robin Carhart-Harris, Jennie N Davis

medRxiv February 19, 2026 preprint DOI: 10.64898/2026.02.18.26346580 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Naturalistic study
Sample size 88
Population Adults 21 years and older participating in Oregon's legal psilocybin services program
Intervention Psilocybin
Dose 27.8 mg total psilocybin equivalents (TPE)
Duration 30-day follow-up
Topics Depression Psilocybin
Keywords Mental health Naturalistic observation Hallucinogen Adverse effect Perception Clinical psychology Psychiatric medication Young adult
Key points Psilocybin sessions under Oregon's regulatory model were associated with significant improvements in depression, anxiety, and well-being 30 days post-session, with no persistent hallucinogen persisting perception disorder at 30 days.

Abstract

Abstract Background In 2020, Oregon became the first U.S. state to establish a regulated framework for adults to access psilocybin services using naturally-derived mushroom products. No studies have examined mental health outcomes among individuals receiving psilocybin in this context.

Aims: To evaluate changes in self-reported symptoms of depression, anxiety, and well-being 30-days post-psilocybin session under the Oregon state-regulated model , and document session-related adverse events and doses consumed.

Methods: This was a naturalistic study (March 2024-April 2025) among adults ≥21 years participating in a legal psilocybin services program. Online surveys were completed pre-session, 1-day, and 30-days post-session. Primary outcomes were change in depression, anxiety, and well-being symptoms pre-session to 30-days post-session evaluated using linear mixed-effects models (random effect: timepoint; fixed effects: sex, concurrent psychiatric medication use, age, session dose [total psilocybin equivalents, TPE, mg: psilocybin mg + 1.39 * psilocin mg]). Adverse events (e.g., hallucinogen persisting perception disorder [HPPD]) were assessed at 1-day and 30-days post-session.

Results: Participants (n=88; median age 43 years; 52% male) were predominantly Oregon residents (53.4%), psychedelic-experienced (64.8%), and concurrently using psychiatric medication (46.6%). All outcomes improved significantly at 30-days post-session (p<0.001), including in sensitivity analyses stratified by concurrent psychiatric medication usage (p<0.001 all outcomes, both groups). Two participants (2.3%) reported symptoms consistent with HPPD at 1-day post-session, but none at 30-days. Mean dose was 27.8 mg (SD 8.2) TPE.

Conclusions: Psilocybin sessions delivered under the Oregon regulatory model were associated with clinically meaningful improvements in depression, anxiety, and well-being 30-days post-session, supporting therapeutic effectiveness of legal psilocybin services.

Comparable studies

Other observational and cohort studies on psilocybin for depression, most cited first.

Study Year Design Participants
Psilocybin for treatment-resistant depression: fMRI-measured brain mechanisms. Patients with treatment-resistant depression 2017 Observational cohort n = 19
Psilocybin with psychological support improves emotional face recognition in treatment-resistant depression Patients with treatment-resistant depression and healthy controls 2017 Observational cohort n = 33
More Realistic Forecasting of Future Life Events After Psilocybin for Treatment-Resistant Depression Patients with treatment-resistant depression (TRD) 2018 Observational cohort n = 15
Natural speech algorithm applied to baseline interview data can predict which patients will respond to psilocybin for treatment-resistant depression. 17 patients with treatment-resistant depression and 18 untreated age-matched healthy... 2018 Observational cohort with machine learning classification n = 35
Brain dynamics predictive of response to psilocybin for treatment-resistant depression. Responders and non-responders to psilocybin therapy for depression 2024 Observational cohort

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