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Not yet recruitingPhase 2

Group PACBT for Depression

NCT07566104 · University of California, Los Angeles

Closed to entry
Status
Not accepting participants
Phase 2
Phase
30
Target enrolment
1
Study sites
1 US states

What it is testing

Summary

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.

Summary as written by the trial’s own sponsor and published on ClinicalTrials.gov API v2. It is the sponsor’s description, reproduced unedited, not an assessment by this site.

What counts as success

Primary outcome measures

  • Treatment acceptability

    Measured over 4 months (Baseline to Post-treatment)

  • Feasibility as measured by participant retention

    Measured over 4 months

  • Hamilton Depression Rating Scale

    Measured over 7 months (Baseline to end of study)

A trial succeeds or fails on its primary outcome, declared in advance. Everything else it reports is secondary by definition.

Who can take part

Eligibility, as published

21 Years to 60 Years
Ages
All
Sex
Not accepted
Healthy volunteers
Inclusion Criteria: * Ages 21-60, * Fluent in English * Able to swallow capsules, * Meets for a current major depressive episode or a history of major depressive episodes based on the DSM-5 criteria (American Psychiatric Association, 2013), * Active current depressive symptoms (i.e., scores \>16 on the Hamilton-Depression Rating Scale covering the prior 2 weeks; Hamilton, 1986), * Have an identified support person (i.e., trusted adult friend or relative) who can pick up the individual from UCLA Semel Institute and drive individual home following psilocybin sessions, * For women of child-bearing potential - using one form of highly effective contraception (e.g., oral contraceptive pill) and willingness to continue contraceptive use for duration of study. Must be willing to take on-site pregnancy tests. * Agree to refrain from any psychoactive drug (including alcohol) within 24 hours of each drug session and during the drug sessions. Participants will be allowed to consume their usual amount of caffeine prior to and after the drug sessions. * Agree to not take any PRN medications on the mornings of the drug sessions * Has been medically cleared for the study by a physician * Participants must remain on anti-hypertensive medications if prescribed previously to manage hypertension Exclusion Criteria: * A personal or family history (first-degree) of psychosis or mania * Resting blood pressure above 140 systolic, 90 diastolic or heart rate \> 90 beats per minute (averaged across four separate measurements) * Meeting criteria for a DSM-5 cluster B personality disorder (narcissistic, histrionic, borderline, antisocial personality disorder), * Active suicidality (i.e., HAM-D item 3 score of greater than 3) or other psychiatric disturbance requiring acute treatment * Current use of antidepressants or other serotonergic-affecting substances (e.g., St. John's Wort and 5-hydroxytryptophan), lithium, or efavirenz \[regardless of whether the drug(s) is/are prescribed for MDD or other conditions\] * Current use of opioids (e.g., codeine, fentanyl, hydrocodone, meperidine, tramadol) * Currently receiving cognitive behavioral therapy, * Any of the following cardiovascular conditions: uncontrolled hypertension, coronary artery disease, congenital long QT syndrome, cardiac hypertrophy, cardiac ischemia, congestive heart failure, myocardial infarction, tachycardia, artificial heart valve, a clinically significant screening ECG abnormality, or any other significant cardiovascular condition * QTc interval measurement of \> 450 ms in males or \> 460 ms in females as measured by the baseline ECG * A history of stroke or Transient Ischemic Attack (TIA) * Epilepsy or history of seizures * Insulin-dependent diabetes * Meeting criteria for a DSM-5 substance abuse or dependence within prior 6 months (including for nicotine and cannabis) * Positive urine drug screen for illicit substances (not including cannabis) * Use of other psychedelics or ketamine within prior 12 months * Adverse prior reaction to a 5-HT2A receptor agonist psychedelic agent * Pregnant, trying to get pregnant, or nursing

Where

1 study site

FacilityCityRegionCountry
UCLA Semel InstituteLos AngelesCaliforniaUnited States

On the registry

Contact the trial directly

This site does not enrol anyone and is not involved in this trial. To ask about taking part, use the sponsor’s own contact details on the official registry record, which is also where the most current version of everything above lives.

Before you do, the preparation checklist lists what a site will ask you on a first call and what is worth asking them. It is free and collects nothing.

NCT07566104 on ClinicalTrials.gov →

Last updated in the registry 2026-05-04. Registry records change; this page reflects the data build of 2026-08-25.

Related

Where this trial sits