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The Safety, Feasibility, and Acceptability of Psilocybin Combined With Multidisciplinary Palliative Care in Demoralized Cancer Survivors With Chronic Pain (P-PC)
This phase I trial evaluates the side effects of psilocybin and how well it works under supportive care conditions in cancer survivors living with demoralization and chronic pain. Cancer patients often experience demoralization, which is characterized by feelings of hopelessness, loss of meaning, and existential distress. Psilocybin psychotherapy, together with multidisciplinary palliative and supportive care, may help treat the anxiety, depression, and chronic pain felt by cancer survivors - defined here as cancer patients from time of diagnosis through the end-of-life.
PRIMARY OBJECTIVE: I. To determine the safety, feasibility, and acceptability of a single administration of 25 mg psilocybin (psilocybin) provided under supportive conditions with multidisciplinary palliative care support (P-PC) in adult cancer survivors living with concurrent demoralization and chronic pain. EXPLORATORY OBJECTIVE: I. To evaluate for changes in demoralization, anxiety, depression, quality of life, pain, other symptoms, mysticism, awe, post-traumatic growth, social isolation, and psychosocial functioning from baseline to end-of-treatment to 3.5-month follow up. OUTLINE: Patients receive psilocybin orally (PO) and undergo observation for up to 8 hours on day 14. After completion of study intervention, patients are followed up on days 15, 21, 42, 56, and 98.
Age
26 - No limit years
Sex
ALL
Healthy Volunteers
No
Emory University/Winship Cancer Institute
Atlanta, Georgia, United States
Brain Health Center at Executive Park
Atlanta, Georgia, United States
Start Date
November 1, 2022
Primary Completion Date
April 25, 2024
Completion Date
January 24, 2025
Last Updated
July 23, 2025
11
ACTUAL participants
Psilocybin
DRUG
Psychotherapy
BEHAVIORAL
Quality-of-Life Assessment
OTHER
Questionnaire Administration
OTHER
Lead Sponsor
Emory University
Collaborators
NCT06311214
NCT04704661
Data Source & Attribution
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