Investigation to Understand and Optimize Psilocybin
This study will examine the effects of a single dose of psilocybin, administered with psychological support, on symptoms of depression. It will also assess whether different post-dosing interventions, including a non-invasive technique called transcutaneous auricular Vagus Nerve Stimulation (taVNS), influence various psychological and behavioral outcomes. In addition, the study will explore objective measures of real-world social behavior and identify early behavioral responses that may be associated with…
Conditions studied
Depression
About this study
This study will examine the effects of a single dose of psilocybin, administered with psychological support, on symptoms of depression. It will also assess whether different post-dosing interventions, including a non-invasive technique called transcutaneous auricular Vagus Nerve Stimulation (taVNS), influence various psychological and behavioral outcomes. In addition, the study will explore objective measures of real-world social behavior and identify early behavioral responses that may be associated with long-term treatment outcomes.
Interventions
- Drug: Psilocybin — The psilocybin used in this study is synthesized under Good Manufacturing Practice (GMP) guidelines and is provided in a capsule containing 25 mg of synthetic psilocybin.
- Device: Transcutaneous Auricular Vagus Nerve Stimulation (taVNS) — Participants will be provided with a taVNS device and trained on its use. The device delivers gentle stimulation to the left ear.
- Device: Sham taVNS — Participants will be provided with a taVNS device and trained on its use. The device delivers gentle stimulation to the left ear. In the sham condition, the device will simulate the sensations of active taVNS without delivering therapeutic stimulation.
Primary outcomes
- Montgomery-Åsberg Depression Rating Scale (MADRS) score (Baseline 2, Week 8 Post-Psilocybin Dosing)
- PROMIS Ability to Participate in Social Roles and Activities - Short Form 8a (Baseline 2, Week 8 Post-Dose)
- Quality of Life Enjoyment and Satisfaction Questionnaire Short-Form (Q-LES-Q) score (Baseline 2, Week 8 Post-Dose)
Eligibility information
Study locations
- Vail Health Behavioral Health, Edwards, Colorado 81632 United States
Source: ClinicalTrials.gov. Record last refreshed by Varda Clinical: 2026-09-27.