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NCT07566104Not yet recruitingPhase 2

Group PACBT for Depression

Group Psilocybin-assisted Cognitive Behavioral Therapy for Major Depressive Disorder

Source: ClinicalTrials.gov · Last updated 4 May 2026

Brief summary (registry, in English)

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.

Status (registry)
Not yet recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
30 (estimated)
First submitted
28 Apr 2026
Start date
Jan 2027
Primary completion date
Dec 2028
Lead sponsor
University of California, Los Angeles
Diseases
Depression
NCT number
NCT07566104

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 30
  • From Jan 2027 to the primary completion date, Dec 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Currently receiving cognitive behavioral therapy,
  • 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

Other illness

  • 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 \[regardless of whether the drug(s) is/are prescribed for MDD or other conditions\]
  • A history of stroke or Transient Ischemic Attack (TIA)
  • Epilepsy or history of seizures
  • Insulin-dependent diabetes

Lab values

  • 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

Other

  • A personal or family history (first-degree) of psychosis or mania
  • Current use of opioids (e.g., codeine, fentanyl, hydrocodone, meperidine, tramadol)
  • Pregnant, trying to get pregnant, or nursing

Who the study is looking for

  • 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

Age in the registry: 21 years to 60 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
UCLA Semel Institute
Coordinator of this site? Confirm its status
Los AngelesUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.