St. Michael's Hospital, Unity Health Toronto
Toronto, Ontario, M5S 1A1, Canada
Location status: Recruiting
NCT Number: NCT06386003
This is an open-label trial evaluating feasibility, tolerability, safety and efficacy of psilocybin assisted cognitive processing therapy for chronic Posttraumatic Stress Disorder (PTSD).
Interested in participating?
Request Info18 year–65 year
All sexes
Interventional
Phase 2
Toronto, Ontario, M5S 1A1, Canada
Location status: Recruiting
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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.
Time frame: Up to 16 weeks
Recruitment rate, withdrawal rate, adherence rate, data completion rate, percentage of participants with severe adverse events.
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.
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.
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).
Time frame: Up to 16 weeks
Total score ranges from 0 to 21; a higher score denotes greater symptom severity.
Time frame: Up to 13 weeks
The Dissociative Experiences Scale II is a 28-item, self-report measure of dissociative experiences.
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.
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.
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.
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.
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.
Time frame: Up to 13 weeks
The BEAQ is a 15-item self-report measure of experiential avoidance.
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.
Time frame: Up to Day 7
The WAI-SF is a patient-rated measure of the alliance between a therapist and client.
Time frame: Up to 13 weeks
The DERS-SF is an 18-item measure used to identify emotional regulation issues in adults.
Time frame: Up to 13 weeks
The SCS-SF is a 12-item self-report measure of self-compassion.
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.
Time frame: Up to Day 3
The EBI is a measure of emotional release/breakthrough experienced during the acute psychedelic state.
Time frame: Up to Day 3
The ASC measures altered states of consciousness.
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.
Time frame: Screening
Time frame: Up to 16 weeks
Example: sleep, activity
Contact information is provided by the study sponsor or research team.
Unity Health Toronto
Other
Psilocybin-Assisted Massed Cognitive Processing Therapy for Chronic Posttraumatic Stress Disorder: An Open-label Trial
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.
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