UCLA Semel Institute
Los Angeles, California, 90095, United States
Location status: Recruiting
NCT Number: NCT07281352
The primary objectives of this clinical investigation are to (1) determine the acceptability and feasibility of joining psilocybin-assisted therapy with cognitive-behavioral therapy (PA-CBT) for patients with depression, (2) optimize CBT to most effectively integrate the psilocybin experience with psychotherapy and (3) examine the clinical benefit of psilocybin as an adjunct to cognitive-behavioral therapy (CBT) for major depressive disorder.
This study is a randomized, two-arm, fixed dose trial that will test the feasibility, acceptability, and participant and therapist adherence to PA-CBT. Both treatment arms will receive two doses of psilocybin (10mg and then 25mg, separated by one month). In Phase II, participants will be randomized (1:1) to either a 12-session PA-CBT or a 6-session standard psilocybin-assisted therapy (PAT) condition (3 hours of preparation plus 3 hours of supportive therapy integration following the psilocybin experiences).
Interested in participating?
Request Info21 year–60 year
All sexes
Interventional
Phase 1 / Phase 2
Los Angeles, California, 90095, United States
Location status: Recruiting
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants will receive two doses of psilocybin (10mg, 25mg).
Twelve total sessions of therapy, including manualized cognitive behavioral therapy for major depressive disorder, including psychoeducation about depression, cognitive skills, and behavioral skills as well as preparation for psilocybin.
Six total therapy sessions. Preparation for psilocybin in the first three sessions plus supportive, nondirective psychotherapy in the final three sessions.
Time frame: 4-month treatment period
Treatment acceptability as measured by the participant. Total scores range from 8 to 32, with the higher number indicating greater satisfaction.
Time frame: 4-month treatment period
Feasibility as measured by the number of participants retained in each treatment condition over the course of the study treatment
Time frame: 7-month study period
symptom severity scored from 0-53, with larger values indicating greater depressive severity
Time frame: 7-month study period
psychosocial functioning scored from 0-100, with larger values indicating better functioning
Contact information is provided by the study sponsor or research team.
University of California, Los Angeles
Other
Psilocybin-Assisted Cognitive Behavioral Therapy for Depression
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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