Trauma-informed Psilocybin Assisted Psychotherapy (TiPAP) for PTSD
Key facts
- Who runs it
- Tel-Aviv Sourasky Medical Center
- Where
- Israel1 site in 1 countryChoose a country to see its sites
- Trial code
- Status
- Recruiting
- Phase
- Early phase 1
- People taking part
- 13 people, planned
- Started
- 22 Jul 2025
- Expected to end
- 31 Dec 2026
- Type of study
- Interventional
- Treatments tested
- Psilocybin (drug)
- Trauma-Focused Psychotherapy
- Record updated
- 30 July 2026
Who can take part
- Age
- 21 years to 65 years
- Sex
- Women and men
- Healthy volunteers
- Cannot take part
The registry criteria, word for word
Show all 26 criteriaShow less
Who can take part
- Age 21-65 years
- Diagnosis of post-traumatic stress disorder (PTSD) according to DSM-5 criteria, as assessed by CAPS-5
- At least 1 year since the traumatic event
- Moderate or greater PTSD severity (CAPS-5 score ≥ 25)
- Ability to provide written informed consent
- Ability to read, write, speak, and understand Hebrew
- Prior trauma-focused psychotherapy
- Medically healthy at screening, as determined by a study physician, including:; No exclusionary medical conditions; Resting blood pressure between 90/60 and 150/90 mmHg and heart rate between 45-100 bpm; Normal laboratory results (including liver function, renal function, and electrolytes)
Who cannot take part
- Use of psychedelic substances within 3 months before enrollment
- Pregnancy, breastfeeding, or positive pregnancy/drug test (excluding cannabis) on the day of dosing
- Use of medications contraindicated with psilocybin
- Changes in psychiatric medication (dose or type) within one month before enrollment
- Current or past diagnosis of psychotic disorders, bipolar disorder, schizoaffective disorder, dissociative identity disorder, or borderline personality disorder (as assessed by MINI or SCID-5-SPQ)
- First-degree relative with a history of a psychotic disorder
- History of antidepressant-induced mania or hypomania
- Substance use disorder (excluding nicotine and caffeine); mild-to-moderate alcohol or cannabis use may be permitted under monitoring and PI approval
- History of adverse psychological reaction to psychedelics requiring hospitalization
- Significant cardiovascular disease, including ischemic heart disease, uncontrolled hypertension, arrhythmia, or heart failure (NYHA class ≥3)
- Dementia or suspected cognitive impairment
- Current psychotic features
- Significant suicidal risk as assessed by the Columbia Suicide Severity Rating Scale (C-SSRS), including active suicidal ideation with intent or plan, or suicidal behavior within the past 6 months
- Participation in a clinical trial involving administration of a psychedelic substance within the past 12 months
- Traumatic brain injury with loss of consciousness >24 hours or post-traumatic amnesia >7 days (unless cleared by neurological evaluation)
- BMI <18 or >33
- Abnormal liver or renal function tests
- Needle phobia or inability to undergo blood testing
Check if you might fit
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 21 and 65 years old?
This trial has no sites in United States.
It has sites in one country. Choose a country to see its sites.
About the trial
What the trial wants to find out
This is an open-label pilot study designed to evaluate the safety, tolerability, and preliminary clinical effects of psilocybin-enhanced trauma-focused psychotherapy in individuals with post-traumatic stress disorder (PTSD).
Read full original descriptionShow less
Participants will receive a structured therapeutic protocol that includes preparatory sessions, two psilocybin administration sessions (15 mg followed by 25 mg), and integration sessions based on a trauma-focused therapeutic approach.
The primary objective of the study is to assess the safety and tolerability of psilocybin administration in this clinical population. Secondary objectives include evaluating changes in PTSD symptom severity, as measured by the Clinician-Administered PTSD Scale (CAPS-5), at 30 days following treatment.
This pilot study will include 13 participants and is intended to inform the feasibility and design of a subsequent randomized controlled trial.
The group in the trial
- Psilocybin-Assisted Trauma-Focused PsychotherapyTreatment being tested
Participants receive a structured clinical intervention combining preparatory psychotherapy sessions, two psilocybin dosing sessions (15 mg and 25 mg), and integration psychotherapy sessions within a trauma-focused therapeutic framework.
Treatment: Psilocybin (drug) and Trauma-Focused Psychotherapy
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorData and sources
- Registry record
- Listed on ClinicalTrials.gov.
- Official title
- Trauma-informed Psilocybin Assisted Psychotherapy (TiPAP) for Post-Traumatic Stress Disorder
- Fit questions
- Built from NCT07737054, who can take part
- Record updated
- 30 July 2026