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| Name | Class |
|---|---|
| Toronto Metropolitan University | OTHER |
| University of Ottawa | OTHER |
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This is an open-label trial evaluating feasibility, tolerability, safety and efficacy of psilocybin assisted cognitive processing therapy for chronic Posttraumatic Stress Disorder (PTSD).
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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Experimental | Experimental | Single dose of psilocybin 25mg + Massed cognitive processing therapy |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| 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. |
| Measure | Description | Time Frame |
|---|---|---|
| Feasibility and tolerability | Recruitment rate, withdrawal rate, adherence rate, data completion rate, percentage of participants with severe adverse events. | Up to 16 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Clinician-Administered PTSD Scale for DSM-5 (CAPS-5) total score | 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. | Up to 16 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Effect on digital physiological passive data collected through the use of a wearable device | Example: sleep, activity | Up to 16 weeks |
Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Venkat Bhat | Contact | 416-360-4000 | 76404 | Venkat.Bhat@unityhealth.to |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| St. Michael's Hospital, Unity Health Toronto | Recruiting | Toronto | Ontario | M5S 1A1 | Canada |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 39823496 | Derived | Meshkat S, J Zeifman R, Stewart K, Janssen-Aguilar R, Lou W, Jetly R, Monson CM, Bhat V. Psilocybin-assisted massed cognitive processing therapy for chronic posttraumatic stress disorder: Protocol for an open-label pilot feasibility trial. PLoS One. 2025 Jan 17;20(1):e0313741. doi: 10.1371/journal.pone.0313741. eCollection 2025. |
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| ID | Term |
|---|---|
| D013313 | Stress Disorders, Post-Traumatic |
| ID | Term |
|---|---|
| D040921 | Stress Disorders, Traumatic |
| D000068099 | Trauma and Stressor Related Disorders |
| D001523 | Mental Disorders |
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| ID | Term |
|---|---|
| D011562 | Psilocybin |
| ID | Term |
|---|---|
| D026121 | Indole Alkaloids |
| D000470 | Alkaloids |
| D006571 | Heterocyclic Compounds |
| D007211 | Indoles |
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| Posttraumatic stress disorder Checklist-5 (PCL-5) | 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. | Up to 16 weeks |
| Patient Health Questionnaire-9 (PHQ-9) | 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). | Up to 16 weeks |
| Generalized Anxiety Disorder Scale, 7-item (GAD-7) | Total score ranges from 0 to 21; a higher score denotes greater symptom severity. | Up to 16 weeks |
| Dissociative Experiences Scale II (DES-II) | The Dissociative Experiences Scale II is a 28-item, self-report measure of dissociative experiences. | Up to 13 weeks |
| Pittsburgh Sleep Quality Index (PSQI) | The PSQI is a self-rated questionnaire which assesses sleep quality and disturbances over a 1-month time interval. | Up to 13 weeks |
| World Health Organization Well-Being Index, 5-item (WHO-5) | 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. | Up to 16 weeks |
| Quality of relationships inventory (QRI) | 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. | Up to 13 weeks |
| Inventory of psychosocial functioning (IPF) | The IPF is an 80-item self-report instrument measuring PTSD-related functional impairment in the past 30 days. | Up to 13 weeks |
| Posttraumatic Maladaptive Beliefs Scale (PMBS) | The PMBS is a 15-item scale that was developed to measure maladaptive beliefs about life circumstances that may occur following trauma exposure. | Up to 13 weeks |
| Brief Experiential Avoidance Questionnaire (BEAQ) | The BEAQ is a 15-item self-report measure of experiential avoidance. | Up to 13 weeks |
| 24-items Multidimensional Psychological Flexibility Inventory (MPFI-24) | The MPFI-24 is a 24-item self-report scale developed to assess the specific components of psychological flexibility and inflexibility. | Up to 13 weeks |
| Working Alliance Inventory- Short Form (WAI-SF) | The WAI-SF is a patient-rated measure of the alliance between a therapist and client. | Up to Day 7 |
| Difficulties in Emotion Regulation Scale-Short Form (DERS-SF) | The DERS-SF is an 18-item measure used to identify emotional regulation issues in adults. | Up to 13 weeks |
| Self-Compassion Scale-Short Form (SCS-SF) | The SCS-SF is a 12-item self-report measure of self-compassion. | Up to 13 weeks |
| Psychological Insight Questionnaire (PIQ) | 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. | Up to Day 3 |
| Emotional Breakthrough Inventory (EBI) | The EBI is a measure of emotional release/breakthrough experienced during the acute psychedelic state. | Up to Day 3 |
| Altered States of Consciousness Rating Scale (ASC) | The ASC measures altered states of consciousness. | Up to Day 3 |
| Acceptance/Avoidance-Promoting Experiences Questionnaire (APEQ) | 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. | Up to Day 3 |
| Childhood Trauma Questionnaire-short form (CTQ-SF) | Screening |
| D006574 |
| Heterocyclic Compounds, 2-Ring |
| D000072471 | Heterocyclic Compounds, Fused-Ring |
| D014363 | Tryptamines |
| D054836 | Indolizidines |
| D007212 | Indolizines |