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NCT04932434CompletedPhase 2

Psilocybin Therapy for Depression and Anxiety in Parkinson's Disease

Psilocybin Therapy for Depression and Anxiety in Parkinson's Disease: a Pilot Study

Source: ClinicalTrials.gov · Last updated 3 Sept 2026

Brief summary (registry, in English)

The purpose of this study is to determine the safety, tolerability, and feasibility of psilocybin therapy for depression and anxiety in people with Parkinson's disease.

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
12 (actual)
First submitted
5 May 2021
Start date
15 Aug 2021
Primary completion date
31 Dec 2024
Lead sponsor
Joshua Woolley, MD, PhD
NCT number
NCT04932434

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 12
  • From 15 Aug 2021 to the primary completion date, 31 Dec 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Regular use of medications that may have problematic interactions with psilocybin, including but not limited to dopamine agonists, MAO inhibitors, N-methyl-D-aspartate (NMDAR) antagonists, antipsychotics, and stimulants

Other illness

  • Significant cognitive impairment
  • A health condition that makes this study unsafe or unfeasible, determined by study physicians

Other

  • Psychotic symptoms involving loss of insight

Who the study is looking for

  • Age 40 to 75
  • Comfortable speaking and writing in English
  • Clinically diagnosed early stage Parkinson's Disease (Hoehn and Yahr Stage 1-3 during an "off" period) who meet DSM-5 criteria for a depressive or anxious disorder and meet all other inclusion and exclusion criteria at screening
  • Currently experiencing depression and/or anxiety (a formal diagnosis is not necessary)
  • Able to attend all in-person visits at UCSF as well as virtual visits
  • Have a care partner/support person available throughout the study
  • Have an established primary care provider, neurologist, or psychiatrist

Age in the registry: 40 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of California San Francisco
Coordinator of this site? Confirm its status
San FranciscoUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.