NCT07226232 · VA Office of Research and Development
Psilocybin Intervention for Veterans Overcoming Treatment-Resistant Depression
(PIVOT)
What this study is about
The purpose of this multi-site randomly assigned controlled trial is to evaluate the effectiveness and risks of psilocybin for the treatment of depression in U.S. military Veterans with and without (±) concurrent posttraumatic stress disorder.
View original scientific description
The purpose of this multi-site randomized controlled trial is to evaluate the efficacy and risks of psilocybin for the treatment of depression in U.S. military Veterans with and without (±) concurrent posttraumatic stress disorder.
Interventions
DRUG
Psilocybin
Psilocybin comparator dose
DRUG
Psilocybin
Psilocybin Intervention Dose
Primary outcome measures
Montgomery-Asberg Rating Scale (MADRS)
Time frame: 2 weeks
10-item clinician-administered rating scale for depression. Scored 0 to 60; higher score indicates more severe symptomatology.
Who can participate
This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.
Inclusion criteria
- Veteran of the U.S. military who is English-speaking
- Signed informed consent and HIPAA
- Adults \</= 75 years of age
- Meets DSM-5 criteria for current major depressive episode (MDE)
- MADRS \>/= 20 at baseline
- Failure to respond satisfactorily to \>/= 2 antidepressant treatments for \>/= 8 weeks, including \>/= 2 weeks at an adequate dose (\>/= 50% of the FDA-approved uppermost dose) for major depression. Augmentation with a medication for depression (e.g., neuroleptics, lithium, levothyroxine) is considered a separate course of treatment.
- If applicable, concurrent \& permitted antidepressants must be at stable doses for \>/= 4 weeks prior to baseline (see allowed \& prohibited medication list)
- Participants of child-bearing potential must have negative pregnancy test \& agree to adhere to a medically acceptable method of birth control during the study
- Has a responsible adult who will provide transportation to the participant's home or place of lodging on the days of psilocybin administration
Exclusion criteria
- Lifetime bipolar, schizophrenia spectrum, or other psychotic disorders
- First-degree relative with history of bipolar I, schizophrenia spectrum or other psychotic disorder
- Presence of psychotic symptoms (e.g., MDE with psychotic symptoms)
- Sedative-hypnotic, stimulant, inhalant and/or opioid use disorder within past 6 months (lifetime substance use disorder is allowed at the discretion of the LSI)
- Severe alcohol and/or cannabis use disorder within the past 6 months (mild or moderate alcohol and/or cannabis use is allowed at the discretion of the LSI)
- Lifetime hallucinogen persisting perception or hallucinogen use disorders
- Use of psilocybin, ayahuasca, mescaline, lysergic acid diethylamide (LSD), dimethyltryptamine (DMT), 5-Methoxy-N,N-dimethyltryptamine (5-MeO-DMT), peyote, or 3,4-methylenedioxymethamphetamine (MDMA) within past XX months
- Participant agrees to not use psychedelics (listed above) during the study, except as prescribed by the study protocol
- Taking prohibited medication within 2 weeks of baseline (see allowed and prohibited concomitant medication list)
- History of severe traumatic brain injury (TBI)
- Diagnosis of dementia or related progressive neurocognitive disorder
- Suicidal ideation/behavior Type 4 or Type 5 intensity on C-SSRS within past 6 months of baseline
- Psychiatric inpatient treatment within past 3 months of baseline
- Treatment with electroconvulsive therapy, deep brain stimulation, vagus nerve stimulation, or transcranial magnetic stimulation within 3 months of baseline
- Implanted central nervous system device
- Treatment with evidence-based psychotherapy (EBP) for MDD or PTSD within 2 weeks prior to baseline. If receiving EBP therapy, he/she must complete treatment at least 2 weeks prior to baseline. Other forms of non-EBP psychotherapy for MDD or PTSD are allowed to continue during the study period.
- Pregnancy or lactation, or anticipated pregnancy or breastfeeding during the active treatment phase
- History of myocardial infarction, congestive heart failure, diabetic ketoacidosis, brain cancer, stroke and/or severe cardiac disease
- Clinically significant cardiac, pulmonary, renal, liver and/or other medical disease that, in the opinion of the investigator, may contraindicate the use of psilocybin, interfere with the interpretation of study results and/or constitute a health risk for the participant if they take part in the study
- Seizure disorder, except for seizures due to fever or withdrawal from a substance
- Clinically significant hypertension (\>160/95 mmHg), hypotension (\<90/60 mmHg) tachycardia (\>100 bpm at rest), QTc prolongation (\>450 msec men; \>470 msec women) or clinically significant arrhythmia on ECG
- Clinically significant abnormal laboratory results on chemistry panel, liver function tests, complete blood count, and/or thyroid stimulating hormone
- Positive urine drug screen for illicit drugs of abuse (except for THC) at screening or baseline
- Prior allergic, adverse reaction or adverse experience to a psilocybin formulation
- Litigating for disability income for a mental disorder outside the VA compensation and pension process
Where
- Birmingham, Alabama
- Tuscaloosa, Alabama
- Portland, Oregon
- Philadelphia, Pennsylvania
- Seattle, Washington
Related conditions & keywords
Frequently asked questions
What is a clinical trial?
A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.
Is it safe to participate?
Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.
Will I be compensated?
Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.
Will I receive a placebo instead of treatment?
When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.
Can I leave a trial if I change my mind?
Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.
How long does a clinical trial last?
Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.
Data: ClinicalTrials.gov · synced Aug 14, 2026 · Source of record for eligibility and locations