UCLA Semel Institute
Los Angeles, California, 90095, United States
NCT Number: NCT07566104
This study will seek to determine the (1) acceptability and (2) feasibility of psilocybin as an adjunct to cognitive-behavioral therapy, delivered as a group treatment (G-PACBT) for major depressive disorder and (3) explore the clinical effects of G-PACBT on depressive symptoms and psychosocial functioning.
Trial opening soon.
Get Notified21 year–60 year
All sexes
Interventional
Phase 2
Los Angeles, California, 90095, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Two administrations of psilocybin, administered orally (a 10mg dose followed by a 25mg dose one month later)
12 sessions of PA-CBT (as manualized by our research team; Weintraub et al., 2023)
Time frame: 4 months (Baseline to Post-treatment)
Treatment acceptability as measured by the participant on the Client Satisfaction Questionnaire-8. Total scores range from 8 to 32, with the higher number indicating greater satisfaction.
Time frame: 4 months
Participant retention over the treatment
Time frame: 7 months (Baseline to end of study)
Depressive symptom severity scored from 0-53, with larger values indicating greater depressive severity
University of California, Los Angeles
Other
Group Psilocybin-assisted Cognitive Behavioral Therapy for Major Depressive Disorder
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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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