Psilocybin-Assisted Therapy for Physician Well-Being and Burnout

NCT ID: NCT06814522

Last Updated: 2025-11-06

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 10 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-12-31
• Study Completion Date: 2026-07-31

Brief Summary

Through an open-label study involving a small group of UCSD physicians experiencing burnout, the investigators will evaluate the feasibility, safety, and preliminary effectiveness of PAT to reduce burnout symptoms.

Detailed Description

Physician burnout is a critical issue. Research shows that physician burnout is increasing, that physicians suffer higher rates of burnout than the general population, and that physician burnout is associated with poor mental health outcomes.

Psilocybin is a naturally occurring alkaloid within certain fungi that elicits acute perceptual, cognitive, and emotional changes when ingested, due to action on neurotransmitter and neurocirculatory systems. The combination of psilocybin with psychological support, termed Psilocybin-Assisted Therapy (PAT), is a promising new mental health intervention shown to produce rapid and sustained improvements in psychological domains affected in burnout. PAT demonstrates preliminary efficacy as a treatment for depression and substance use disorders, is associated with brain changes measured with electroencephalography (EEG) and is a strong candidate treatment for physician burnout.

The primary aim of this study is to investigate the safety, feasibility, and preliminary efficacy of PAT to enhance well-being in University of California, San Diego (UCSD) physicians experiencing burnout. A secondary aim is to identify neurophysiological changes associated with response to PAT. Physicians experiencing burnout will be recruited in an open-label trial involving preparatory therapy sessions, psilocybin treatment, and post-treatment integration. Burnout will be measured with the Stanford Professional Fulfillment Index (PFI).

Conditions

Burnout; Burnout, Healthcare Workers

Keywords

burnout; physician; doctor

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Psilocybin-Assisted Therapy

Subjects will receive a single dose of psilocybin in conjunction with psychedelic-assisted therapy.

Group Type: EXPERIMENTAL

Psilocybin, [3-[2-(dimethylamino)ethyl]-1H-indol-4-yl] dihydrogen phosphate

Intervention Type: DRUG

25 mg, single dose of psilocybin

Interventions

Psilocybin, [3-[2-(dimethylamino)ethyl]-1H-indol-4-yl] dihydrogen phosphate

25 mg, single dose of psilocybin

Intervention Type: DRUG

Other Intervention Names

Psilocybin

Eligibility Criteria

Inclusion Criteria

1. UCSD faculty physician, aged 21-70. Volunteer faculty are not included

2. Meets criteria for physician burnout

3. Experiencing symptoms of burnout for >6 months

4. Able to complete all required study visits

5. Not previously diagnosed with a serious mental illness (including schizophrenia, bipolar disorder, and severe depression), or substance use disorder as confirmed in clinical interview

6. Not currently taking any psychotropic medications or nonpsychotropic medication that may be associated with serotonin syndrome, such as serotonin reuptake inhibitors (SSRI or SNRI), dextromethorphan, linezolid, tramadol, meperidine

Exclusion Criteria

1. Previous inpatient psychiatric hospitalization(s)

2. Previously diagnosed with a psychotic disorder (schizophrenia, schizoaffective disorder, or other psychotic spectrum disorder), bipolar spectrum disorder, personality disorder (borderline personality disorder, antisocial personality disorder, or other severe personality disorders), any severe psychiatric disorder.

3. Exhibiting elevated suicide risk

4. First degree family history of psychosis or bipolar disorder

5. Prior exposure to psilocybin or other psychedelic compounds in the previous 10 years

6. Currently pregnant, nursing, planning pregnancy, engaging in sexual intercourse without effective contraceptive method in last three months

7. Those who plan to donate sperm within three months following the study.

8. Known cardiovascular disease including history of stroke, myocardial infarction, uncontrolled hypertension, valvular heart disease, tachycardia, elongated QT interval, or clinically significant arrythmia.

9. History of seizure disorder

10. Use of recreational illicit drugs

11. Clinically concerning results from vital signs, ECG, physical examination, or laboratory tests during screening

12. Any other clinically significant illnesses deemed to pose risk for the participant

• Minimum Eligible Age: 21 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of California, San Diego

OTHER

Sponsor Role: lead

Responsible Party

Cory Weissman

Dr. Cory Weissman

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

UC San Diego

San Diego, California, United States

Site Status: RECRUITING

Countries

United States

Central Contacts

Jessie Kim

Role: CONTACT

Phone: 619-494-0037

Email: jbk005@health.ucsd.edu

Cory Weissman

Role: CONTACT

Email: cweissman@health.ucsd.edu

Facility Contacts

Jessie Kim

Role: primary

Other Identifiers

811381

Identifier Type: -

Identifier Source: org_study_id