Preliminary safety and effectiveness of psilocybin-assisted therapy in adults with fibromyalgia: an open-label pilot clinical trial
Jenna McAfee, Avinash Hosanagar, Vijay Tarnal, Cody Weston, Katherine Scott, Jamarie Geller, Niloufar Pouyan, Jeffrey Guss, Jacob S. Aday, Deirdre A. Conroy, Diane Horowitz, Steven E. Harte, Nicolas G. Glynos, Anne Baker, Alan K. Davis, Helen J. Burgess, George A. Mashour, Daniel J. Clauw, Kevin F. Boehnke
Frontiers in Pain Research March 18, 2025 DOI: 10.3389/fpain.2025.1527783 (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Open-label pilot clinical trial Randomized Peer reviewed |
|---|---|
| Sample size | 5 |
| Population | People with fibromyalgia |
| Intervention | Psilocybin-assisted therapy |
| Dose | 15 mg and 25 mg |
| Duration | Two doses delivered two weeks apart, with one-month follow-up after second dose |
| Topics | Psilocybin |
| Keywords | Clinical trial Fibromyalgia Open label Pilot trial Physical therapy |
| Citations | 18 |
| Registration | NCT05128162 |
| Key findings | Psilocybin-assisted therapy was well-tolerated and associated with clinically meaningful improvements in pain severity, pain interference, and sleep disturbance in people with fibromyalgia. |
Abstract
Introduction: Fibromyalgia (FM) is the prototypical nociplastic pain condition, characterized by widespread pain and issues with cognition, mood, and sleep. Currently, there are limited treatment options available that effectively treat FM symptoms. Psilocybin-assisted therapy (PAT) is an emerging combined drug-therapy intervention, but no studies to-date have investigated PAT for FM.
Methods: Here, we report findings from an open-label, pilot clinical trial of PAT for FM ( N = 5). In conjunction with psychotherapy (two preparatory, four integration sessions), participants received two doses of oral psilocybin (15 mg and 25 mg) delivered two weeks apart.
Results: Regarding safety (primary outcome), there were transient elevations of blood pressure or heart rate during dosing which normalized by the end of treatment, with no serious adverse events. Four of five participants reported transient headaches following dosing. Compared to baseline, participants reported clinically meaningful improvements in the following secondary outcomes one month following their second psilocybin dose (reported as Cohen's d ): pain severity [ d = −2.1, 95% CI(−3.7 to −0.49)], pain interference [ d = −1.8, 95% CI (−3.27 to −0.24)], and sleep disturbance [ d = −2.5, 95% CI (−4.21 to −0.75)]. Using the Patient Global Impression of Change, one participant reported their symptoms “very much improved,” two reported “much improved,” and two reported “minimally improved.” We stopped recruitment early because of concerns about generalizability and changes in FDA guidance for psychedelic clinical trials that occurred data collection.
Discussion: This small open-label trial preliminarily supports that PAT is well-tolerated by people with FM, establishing a basis for larger randomized controlled trials. Clinical Trial Registration ClinicalTrials.gov , identifier, (NCT05128162).
Comparable studies
Other non-randomized and open-label trials on psilocybin, most cited first.
| Study | Year | Design | Participants |
|---|---|---|---|
| Psilocybin with psychological support for treatment-resistant depression: an open-label feasibility study. Patients with moderate-to-severe, unipolar, treatment-resistant major depression | 2016 | Open-label feasibility trial | n = 12 |
| Psilocybin with psychological support for treatment-resistant depression: six-month follow-up. Patients with severe, unipolar, treatment-resistant major depression | 2017 | Open-label trial | n = 20 |
| Pilot study of the 5-HT2AR agonist psilocybin in the treatment of tobacco addiction Psychiatrically healthy nicotine-dependent smokers | 2014 | Open-label pilot study | n = 15 |
| Quality of Acute Psychedelic Experience Predicts Therapeutic Efficacy of Psilocybin for Treatment-Resistant Depression Patients with treatment-resistant depression | 2018 | Clinical trial | n = 20 |
| Safety, Tolerability, and Efficacy of Psilocybin in 9 Patients With Obsessive-Compulsive Disorder Subjects with obsessive-compulsive disorder (OCD) | 2006 | Controlled clinical trial |
Citations in the library
Cited by 16
- Emerging mechanisms of psilocybin-induced neuroplasticity TIPS - Trends in Pharmacological Sciences September 16, 2025
- Classic Psychedelics in Pain Modulation: Mechanisms, Clinical Evidence, and Future Perspectives ACS Chemical Neuroscience June 6, 2025
- Psychedelic medicine: mechanisms, evidence, and translation to practice BMJ February 23, 2026
- No evidence of immediate or persistent analgesic effect from a single dose of psilocybin in three mouse models of pain Nature Communications January 22, 2026
- Modification of natural tryptamines for the treatment of neuropsychiatric diseases Journal of Psychopharmacology October 4, 2025
and 11 more in the library
Cites 46
- Psilocybin produces substantial and sustained decreases in depression and anxiety in patients with life-threatening cancer: A randomized double-blind trial Journal of Psychopharmacology November 30, 2016
- Rapid and sustained symptom reduction following psilocybin treatment for anxiety and depression in patients with life-threatening cancer: a randomized controlled trial Journal of Psychopharmacology November 30, 2016
- Psilocybin with psychological support for treatment-resistant depression: an open-label feasibility study. The Lancet Psychiatry May 17, 2016
- Effects of Psilocybin-Assisted Therapy on Major Depressive Disorder JAMA Psychiatry November 4, 2020
- Pilot Study of Psilocybin Treatment for Anxiety in Patients With Advanced-Stage Cancer Archives of General Psychiatry September 7, 2010
and 41 more in the library