Pragmatic Trial of Psilocybin Therapy in Palliative Care
Start Date
1/19/2025
Completion Date
12/31/2027
Summary
This multicenter, triple-blind, phase 2, randomized controlled trial will evaluate the efficacy and safety of psilocybin therapy compared to an active control in treating demoralization in adults near the end of life (≤2 years life expectancy).
Detailed Description
After providing written informed consent, participants deemed eligible for this trial will be randomized to a brief course of talk therapy plus 1 dose of oral psilocybin vs the same brief course of talk therapy plus 1 dose of oral ketamine (the active control). Participants' degree of demoralization and other clinical outcomes (e.g., depression, anxiety) will be assessed at 1, 2, and 5 weeks after the study drug administration. After completing the study, participants will have the option of being told which study drug they took (aka, "unblinded"); those who were randomized to the active control will be offered another brief course of talk therapy plus 1 dose of oral psilocybin, and the same sequence of outcome assessments.
Eligibility Criteria
Age Range: 18 years to No maximum
Interventions
Psilocybin
Ketamine
Conditions
Locations
Marin Cancer Care
Greenbrae, California 94904
United States
University of California, Los Angeles
Los Angeles, California 90095
United States
University of San Francisco
San Francisco, California 94518
United States
Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center
Torrance, California 90502
United States
Sunstone Therapies
Rockville, Maryland 20850
United States