Skip to main content
OpenTrials
Recruiting

NCT Number: NCT06386003

Psilocybin-Assisted Cognitive Processing Therapy for Chronic PTSD

This is an open-label trial evaluating feasibility, tolerability, safety and efficacy of psilocybin assisted cognitive processing therapy for chronic Posttraumatic Stress Disorder (PTSD).

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

St. Michael's Hospital, Unity Health Toronto

Toronto, Ontario, M5S 1A1, Canada

Location status: Recruiting

Location contact

Venkat Bhat

CONTACT

[email protected]

4163604000

About this study

Current front-line treatments for Posttraumatic stress disorder (PTSD) are ineffective for up to half of patients, with serious medical and societal consequences. It is imperative to improve the efficacy of front-line treatment options, such as cognitive processing therapy (CPT). CPT is an effective treatment for PTSD, including when delivered intensively (i.e., multiple sessions over 7 days). However, a substantial proportion of patients continue to meet criteria for PTSD or have residual PTSD symptoms post-treatment. Psilocybin-assisted CPT may be a potential solution, as preliminary evidence supports the potential of psilocybin to alleviate symptoms of PTSD.

Fifteen participants will receive a single dose of psilocybin 25mg combined with 12 sessions of massed CPT, and 2 psychotherapy sessions related to psilocybin over 7 days. Participants will complete clinician-administered scales, self-reported mental health questionnaires, and use a wearable device. After the 1-week interventional period, participants will enter a 12-weeks follow-up period.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Meet Diagnostic and Statistical Manual-5th edition (DSM-5) criteria for current PTSD with a duration of 6 months or longer assessed by study psychiatrist;
  • Have a Clinician-Administered PTSD Scale for DSM-5 (CAPS-5) score of 50 or higher, indicating moderate to severe PTSD symptoms;
  • Are willing to refrain from taking any psychiatric medications during the study period.

Exclusion criteria

  • Are pregnant or nursing, or are women of child bearing potential who are not practicing an effective means of birth control;
  • Have a history of or a current primary diagnosis of psychotic disorder, schizophrenia, delusional disorder, borderline personality disorder, schizoaffective disorder, bipolar disorder or, dissociative identity disorder;
  • Have evidence or history of coronary artery disease or cerebral or peripheral vascular disease, hepatic disease with abnormal liver enzymes, or any other medical disorder judged by the investigator to significantly increase the risk of psilocybin administration;
  • Have hypertension using the standard criteria of the American Heart Association (values of 140/90 or higher assessed on three separate occasions;
  • History of seizure disorder;
  • Uncontrolled insulin-dependent diabetes;
  • Recent stroke, intracranial or subarachnoid hemorrhage (< 1 year from signing of informed consent form [ICF]), recent myocardial infarction (< 1 year from signing of ICF), clinically significant arrhythmia (< 1 year from signing of ICF);
  • Have liver disease with the exception of asymptomatic subjects with Hepatitis C who have previously undergone evaluation and successful treatment;
  • Lifetime history of substance-induced psychosis;
  • Lifetime history of substance use disorder with a hallucinogen;
  • History of alcohol use disorder in the past 3 months.

Treatment and study plan

Psilocybin

Drug

Participants will receive a single dose of psilocybin 25mg combined with 12 sessions of massed CPT, and 2 psychotherapy sessions related to psilocybin over 7 days.

Primary outcomes

  1. Feasibility and tolerability

    Time frame: Up to 16 weeks

    Recruitment rate, withdrawal rate, adherence rate, data completion rate, percentage of participants with severe adverse events.

Secondary outcomes

  1. Clinician-Administered PTSD Scale for DSM-5 (CAPS-5) total score

    Time frame: Up to 16 weeks

    The CAPS-5 is a semi-structured clinical interview used to assess index history of DSM-5-defined traumatic event exposure, including the most distressing event, time since exposure, and total number of exposures, as well as frequency and severity of posttraumatic stress symptoms.

  2. Posttraumatic stress disorder Checklist-5 (PCL-5)

    Time frame: Up to 16 weeks

    The PCL-5 is self-report questionnaire in which respondents indicate the presence and severity of PTSD symptoms, derived from the DSM-5 symptoms of PTSD.

  3. Patient Health Questionnaire-9 (PHQ-9)

    Time frame: Up to 16 weeks

    The PHQ-9 is a self-rated measure of depressive symptom severity in the past two weeks. Each of the nine items is rated on a Likert scale, ranging from 0 (not at all) to 3 (nearly every day), and summed for a total score between 0 (no symptoms) to 27 (most severe).

  4. Generalized Anxiety Disorder Scale, 7-item (GAD-7)

    Time frame: Up to 16 weeks

    Total score ranges from 0 to 21; a higher score denotes greater symptom severity.

  5. Dissociative Experiences Scale II (DES-II)

    Time frame: Up to 13 weeks

    The Dissociative Experiences Scale II is a 28-item, self-report measure of dissociative experiences.

  6. Pittsburgh Sleep Quality Index (PSQI)

    Time frame: Up to 13 weeks

    The PSQI is a self-rated questionnaire which assesses sleep quality and disturbances over a 1-month time interval.

  7. World Health Organization Well-Being Index, 5-item (WHO-5)

    Time frame: Up to 16 weeks

    The WHO-5 is a measure of overall well-being, rated on a scale of 0 to 25, with higher scores denoting higher quality of life.

  8. Quality of relationships inventory (QRI)

    Time frame: Up to 13 weeks

    The QRI is a self-report questionnaire used to determine the quality relationships consisting of 25 items that are evaluated on a 4-point Likert scale ranging from 1 = not true to 4 = almost always true.

  9. Inventory of psychosocial functioning (IPF)

    Time frame: Up to 13 weeks

    The IPF is an 80-item self-report instrument measuring PTSD-related functional impairment in the past 30 days.

  10. Posttraumatic Maladaptive Beliefs Scale (PMBS)

    Time frame: Up to 13 weeks

    The PMBS is a 15-item scale that was developed to measure maladaptive beliefs about life circumstances that may occur following trauma exposure.

  11. Brief Experiential Avoidance Questionnaire (BEAQ)

    Time frame: Up to 13 weeks

    The BEAQ is a 15-item self-report measure of experiential avoidance.

  12. 24-items Multidimensional Psychological Flexibility Inventory (MPFI-24)

    Time frame: Up to 13 weeks

    The MPFI-24 is a 24-item self-report scale developed to assess the specific components of psychological flexibility and inflexibility.

  13. Working Alliance Inventory- Short Form (WAI-SF)

    Time frame: Up to Day 7

    The WAI-SF is a patient-rated measure of the alliance between a therapist and client.

  14. Difficulties in Emotion Regulation Scale-Short Form (DERS-SF)

    Time frame: Up to 13 weeks

    The DERS-SF is an 18-item measure used to identify emotional regulation issues in adults.

  15. Self-Compassion Scale-Short Form (SCS-SF)

    Time frame: Up to 13 weeks

    The SCS-SF is a 12-item self-report measure of self-compassion.

  16. Psychological Insight Questionnaire (PIQ)

    Time frame: Up to Day 3

    The PIQ is a 23-item self-report measure of acute experiences of insight (e.g. awareness into emotions, behaviors, beliefs, memories, or relationships) after taking a psychedelic.

  17. Emotional Breakthrough Inventory (EBI)

    Time frame: Up to Day 3

    The EBI is a measure of emotional release/breakthrough experienced during the acute psychedelic state.

  18. Altered States of Consciousness Rating Scale (ASC)

    Time frame: Up to Day 3

    The ASC measures altered states of consciousness.

  19. Acceptance/Avoidance-Promoting Experiences Questionnaire (APEQ)

    Time frame: Up to Day 3

    The APEQ is a psychometric self-report tool for measuring aspects of the acute psychedelic experience that are associated with longer-term changes in psychological flexibility.

  20. Childhood Trauma Questionnaire-short form (CTQ-SF)

    Time frame: Screening

Other outcomes

  1. Effect on digital physiological passive data collected through the use of a wearable device

    Time frame: Up to 16 weeks

    Example: sleep, activity

Study contacts

Contact information is provided by the study sponsor or research team.

Venkat Bhat

CONTACT

[email protected]

416-360-4000 ext. 76404

Sponsors and collaborators

Lead sponsor

Unity Health Toronto

Other

Collaborators

  • Toronto Metropolitan University
  • University of Ottawa

Registry information

Official study title

Psilocybin-Assisted Massed Cognitive Processing Therapy for Chronic Posttraumatic Stress Disorder: An Open-label Trial

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Apr 26, 2024
Registry last updated
Jun 26, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.