62 Participants Needed

Psilocybin-assisted CBT for Depression

AS
SG
Overseen ByShelby Grody
Age: 18 - 65
Sex: Any
Trial Phase: Phase < 1
Sponsor: University of California, Los Angeles
Stay on Your Current MedsYou can continue your current medications while participating
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Approved in 2 JurisdictionsThis treatment is already approved in other countries

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial explores whether combining psilocybin, a psychedelic substance, with cognitive-behavioral therapy (CBT) can help treat major depression. The researchers aim to determine if this combination is practical, accepted by participants, and effective. In the first phase, all participants receive psilocybin and CBT. In the second phase, participants divide into two groups to compare different therapy approaches. Individuals experiencing ongoing depression with past episodes might be suitable if they have a support person to assist them after sessions. As an Early Phase 1 trial, this research focuses on understanding how the treatment works in people, offering participants a chance to be among the first to receive this innovative therapy.

Will I have to stop taking my current medications?

Yes, you will need to stop taking antidepressants or other medications that affect serotonin, like St. John's Wort, to participate in this trial.

Is there any evidence suggesting that this trial's treatments are likely to be safe?

Research shows that psilocybin, the active ingredient in "magic mushrooms," is under study for its effects on depression. Studies have found that psilocybin is usually safe for people to take. In earlier studies, most participants experienced mild and short-lived side effects, such as nausea, headaches, or mood changes. Serious side effects are rare.

Researchers are investigating psilocybin because it might help improve mood and emotional processing. While the FDA has not yet approved psilocybin for treating depression, it has been studied for other mental health issues, providing some evidence of its safety. However, individual experiences can vary, so discussing potential risks with a healthcare professional is crucial.12345

Why are researchers excited about this trial's treatments?

Unlike the standard treatments for depression, which often involve SSRIs or SNRIs that adjust serotonin levels gradually, psilocybin is a psychedelic compound that can potentially provide rapid relief by profoundly altering brain connectivity and thought patterns. Researchers are excited about psilocybin-assisted cognitive-behavioral therapy (CBT) because it combines the lasting insights gained from guided psychedelic experiences with the practical skills of CBT, potentially enhancing overall treatment efficacy. Additionally, the use of psilocybin in conjunction with minimal supportive therapy offers an alternative approach that could benefit those who may not respond well to traditional antidepressants.

What evidence suggests that this trial's treatments could be effective for depression?

Research shows that psilocybin, a substance found in certain mushrooms, may help treat depression. In this trial, participants will receive psilocybin with either minimal supportive therapy or cognitive-behavioral therapy (CBT). Studies have found that psilocybin can greatly reduce depression symptoms when combined with therapy. It seems to enhance CBT—a type of talk therapy that helps change negative thinking. Early results suggest that people receiving psilocybin-assisted therapy feel better emotionally and have improved moods. This treatment affects serotonin receptors in the brain, which can change mood and perception. While more research is needed, these early findings are promising for those seeking new ways to manage depression.12346

Are You a Good Fit for This Trial?

This trial is for adults aged 21-60 with depression, who are experiencing a major depressive episode. They must be able to swallow capsules and have someone to drive them home after sessions. Women should use effective contraception. Exclusions include active suicidality, current antidepressant use, certain cardiovascular conditions, insulin-dependent diabetes, history of psychosis or bipolar in the family, prior adverse reaction to psychedelics, pregnancy or nursing.

Inclusion Criteria

Patient has been medically cleared for the study by a physician
For women of child-bearing potential - using one form of highly effective contraception and willingness to continue contraceptive use for duration of study
I have been diagnosed with major depression now or in the past.
See 4 more

Exclusion Criteria

I am currently undergoing cognitive behavioral therapy.
Adverse prior reaction to a psychedelic agent
I have a heart condition.
See 12 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Phase I Treatment

Open trial of PA-CBT with two doses of psilocybin (10mg and 25mg) and 12 sessions of cognitive behavioral therapy

4 months
12 therapy sessions

Phase II Treatment

Randomized trial with two arms: 12-session PA-CBT or 6-session standard psilocybin-assisted therapy, both with two doses of psilocybin

4 months
6-12 therapy sessions

Follow-up

Participants are monitored for safety and effectiveness after treatment

3 months

What Are the Treatments Tested in This Trial?

Interventions

  • Psilocybin
Trial Overview The study tests combining psilocybin (a psychedelic drug) with cognitive-behavioral therapy (CBT) for treating major depressive disorder. Participants will receive two oral doses of psilocybin during twelve CBT sessions over four months and then be followed up for three additional months.
How Is the Trial Designed?
2Treatment groups
Experimental Treatment
Active Control
Group I: Psilocybin + CBTExperimental Treatment2 Interventions
Group II: Psilocybin + Minimal supportive therapyActive Control2 Interventions

Find a Clinic Near You

Who Is Running the Clinical Trial?

University of California, Los Angeles

Lead Sponsor

Trials
1,594
Recruited
10,430,000+

National Center for Complementary and Integrative Health (NCCIH)

Collaborator

Trials
886
Recruited
677,000+

Published Research Related to This Trial

A single, moderate dose of psilocybin significantly reduced depressive symptoms in 52 participants with major depressive disorder, showing a decrease of 13.0 points on the MADRS scale compared to baseline, which was significantly greater than the placebo group.
54% of participants in the psilocybin group met the criteria for remission of depression 14 days after treatment, and no serious adverse events were reported, indicating a favorable safety profile for this novel treatment.
Single-dose psilocybin-assisted therapy in major depressive disorder: A placebo-controlled, double-blind, randomised clinical trial.von Rotz, R., Schindowski, EM., Jungwirth, J., et al.[2023]
In a study involving 12 healthy adults, escalating doses of psilocybin (0.3, 0.45, and 0.6 mg/kg) were administered safely, with no serious adverse events reported, indicating a favorable safety profile for this psychedelic compound.
The pharmacokinetics of psilocin, the active metabolite of psilocybin, were linear across the tested doses, with an elimination half-life of about 3 hours, suggesting that no dose adjustments are necessary for individuals with mild to moderate renal impairment.
Pharmacokinetics of Escalating Doses of Oral Psilocybin in Healthy Adults.Brown, RT., Nicholas, CR., Cozzi, NV., et al.[2022]
Psilocybin has shown significant therapeutic effects in reducing symptoms of depression and anxiety in patients with life-threatening diseases, based on a systematic review and meta-analysis of clinical trials involving 92 patients.
The results indicate that psilocybin may be a safe and effective treatment option, particularly for cases resistant to conventional therapies, with significant improvements measured by the Beck Depression Inventory and State-Trait Anxiety Inventory.
Psilocybin as a New Approach to Treat Depression and Anxiety in the Context of Life-Threatening Diseases-A Systematic Review and Meta-Analysis of Clinical Trials.Vargas, AS., Luís, Â., Barroso, M., et al.[2020]

Citations

PsilocybinPsilocybin, also known as 4-phosphoryloxy-N,N-dimethyltryptamine (4-PO-DMT), is a naturally occurring tryptamine alkaloid and investigational drug found in ...
Psilocybin | C12H17N2O4P | CID 10624 - PubChem - NIHPsilocybin is a tryptamine alkaloid that is N,N-dimethyltryptamine carrying an additional phosphoryloxy substituent at position 4. The major hallucinogenic ...
Psilocybine - the NIST WebBookPsilocybine's formula is C12H17N2O4P, molecular weight is 284.2481, CAS number is 520-52-5, and also known as Psilocybin.
ZFIN ChEBI: psilocybinA tryptamine alkaloid that is N,N-dimethyltryptamine carrying an additional phosphoryloxy substituent at position 4. The major hallucinogenic alkaloid isolated ...
Definition of psilocybine - NCI Drug DictionaryA tryptamine alkaloid, isolated from various genera of fungi including the genus Psilocybe, with hallucinogenic, anxiolytic, and psychoactive activities.
PsilocinPsilocin, also known as 4-hydroxy-N,N-dimethyltryptamine (4-HO-DMT), is a substituted tryptamine alkaloid and a serotonergic psychedelic.
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