Study of Psilocybin for Anorexia in Young Adults (NCT06399263)
🩺 Plain-English Summary (8th-Grade Level)
This is a single site trial of psilocybin therapy for the treatment of refractory Anorexia Nervosa in young adults. The psilocybin therapy will include three preparatory sessions, psilocybin dosing session one (20mg), two integration sessions, psilocybin dosing session two (up to 25mg), and three final integration sessions. Eating disorder symptoms will be measured pre and post treatment. One to two family member(s) of each young adult participant will be enrolled in the study. One of which will be required to attend a portion of two preparatory sessions and a portion of two integration sessions and receive psychoeducation about supporting the young adult participant through preparation and integration for psilocybin therapy. Investigators hypothesize that psilocybin will increase cognitive flexibility and that this increase will predict long-term changes in cognitive rigidity, habitual eating, and exercise behaviors in patients with Anorexia Nervosa.
Who can join: Review the eligibility criteria below.
Location: University of California, San Francisco — San Francisco, California
Age range: 18 Years to 25 Years
🧪 Interventions in This Study
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (2 Sites)
- University of California, San Francisco — San Francisco, California
- University of California, San Francisco — San Francisco, California
📞 Contact the Study Coordinator
Phone: (415) 993-2486
Email: psilocybin.an.study@ucsf.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Anorexia Nervosa
- Role of CBD in Regulating Meal Time Anxiety in Anorexia Nervosa — San Diego, California
- Developing an EEG Paradigm to Study Prediction Error in Anorexia Nervosa — San Diego, California
- Identifying Networks Underlying Compulsivity in Anorexia Nervosa for Targeting With Neuromodulation — San Francisco, California
- Investigation of Multi-Family Therapy for Anorexia Nervosa — Chicago, Illinois
- Appetitive Conditioning in Anorexia Nervosa — Toronto, Ontario
- Incorporating Narrative Into the Treatment of Youth With Anorexia Nervosa (Virtual) — San Francisco, California
Explore by condition: All Anorexia Nervosa clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.