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Pilot Study on the Effects of Psilocybin on Belief Updating and Insight Formation

2026年9月8日 更新者:Brown University
The primary aim of this phase I mechanistic pilot study is to evaluate the effects of psilocybin on aspects of cognition in healthy adult volunteers. Up to 24 participants will receive a single dose of either psilocybin or inert placebo, and they will be asked to complete several computer-based behavioral tasks measuring features of learning, belief updating, and abstraction. Participants will also complete measures of subjective experience and expectancy, as well as semi-structured interviews at follow up, to assess whether experience correlates with behavior. This is a Voluntary Submission.

調査の概要

状態

まだ募集していません

条件

研究の種類

介入

入学 (推定)

24

段階

  • フェーズ 1

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

    • Rhode Island
      • Providence、Rhode Island、アメリカ、02903
        • Brown University School of Public Health
        • コンタクト:

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

はい

説明

Inclusion Criteria:

  1. be at least 18 years old at time of signing informed consent
  2. be fluent in speaking and reading English
  3. be able to swallow pills (capsules)
  4. agree to use highly effective birth control for at least one month prior to enrollment, and for the duration of study enrollment, whether male or female assigned at birth. Acceptable methods include: copper or hormonal coil intrauterine device (IUD), implanted or injected hormonal method, documented permanent sterilization, documented not able to become pregnant, or oral/intravaginal/transdermal hormones plus a barrier contraception. Two forms of contraception are required with any barrier method or with any oral, intravaginal, or transdermal hormonal method due to these methods not being considered highly effective alone. Abstinence alone is not an acceptable contraceptive method for this study.
  5. be healthy and psychologically stable as determined by screening for medical and psychiatric problems via a clinical interview, a medical questionnaire, a physical examination, an electrocardiogram (ECG), and routine laboratory tests
  6. agree to inform investigators within 48 hours of any new medical conditions, treatments, or procedures
  7. agree to refrain from using any psychoactive or recreational drugs, including cannabis, for the duration of study enrollment (with the exception of limited alcohol, nicotine, and caffeine as below)
  8. agree to refrain from drinking alcohol within 24 hours of all experimental sessions
  9. agree to consume approximately the same amount of caffeine and nicotine as on a usual day before experimental sessions, but to not consume any nicotine or caffeine closer than 1 hour prior to the scheduled dosing time. If the participant does not routinely consume caffeine or nicotine, they must agree not to do so for the duration of the study.
  10. agree to refrain from taking any "as needed" or "over the counter" medications (e.g., medications for pain, insomnia, or allergies) within 24 hours of all experimental sessions, unless previously approved by a study physician
  11. agree to store their phone and car keys in a locked storage locker for the duration of the experimental dosing session, and agree to stay on site for at least 6 hours after drug administration and until a physician agrees they are safe to leave the premises
  12. be able to identify two trusted support people (e.g. friend or family member, at least age 18 years of age), who are willing and able to serve as an emergency contact, and to pick the participant up and transport them home after the dosing session. One of these will be designated the primary support person, and the second will be backup to pick the person up in the event that the primary becomes unavailable.
  13. agree to not drive a motor vehicle or heavy machinery for 24 hours after the dosing session
  14. have used a classical psychedelic (5-HT2A agonist, such as psilocybin, LSD, DMT, 5-MeO-DMT, ayahuasca, mescaline) at least once in lifetime without clinically significant adverse effects

Exclusion Criteria:

  1. have used any psychedelic, hallucinogen, or entactogen, including 3,4-methylenedioxymethamphetamine (MDMA) and ketamine/esketamine, but not including cannabis, within the past 3 months
  2. unwilling or unable to stop using cannabis a minimum of one week prior to enrollment and to refrain from cannabis use for the duration of the study enrollment, to be tested with urine drug screens
  3. currently pregnant (as indicated by a positive urine pregnancy test assessed at intake and before the drug session), nursing, intending to become pregnant within 3 months of enrollment, intending to father a child within 3 months of enrollment, intending to donate sperm or eggs within 3 months of enrollment, or not practicing a highly effective means of birth control as noted in the Inclusion Criteria.
  4. history of traumatic brain injury, or history of seizure disorder in adulthood
  5. history of any clinically significant cardiovascular condition, or condition that could make receiving the study drug harmful because of increases in blood pressure and heart rate. This includes, but is not limited to, uncontrolled hypertension, coronary artery disease, heart failure, stroke, myocardial infarction, artificial heart valve, aneurism, or clinically significant arrhythmia. Uncontrolled hypertension is defined here as repeated blood pressure readings of >= 140 mmHg systolic or >= 90 mmHg diastolic.
  6. baseline QTc > 450 milliseconds (QTc is defined as the QT interval corrected for heart rate, either machine-read or manually over-read)
  7. current poorly controlled or insulin dependent diabetes mellitus (type I or type II)
  8. current clinically significant respiratory condition (supplemental oxygen requirement, or requiring hospitalization within the last year)
  9. current clinically significant liver or biliary disease, including recent laboratory abnormalities (AST or ALT > 3x institutional upper limit of normal (ULN); total bilirubin > 1.5 x ULN or direct bilirubin < 35%), or based on the presence of ascites, encephalopathy, jaundice, esophageal varices, or coagulopathy
  10. clinically significant renal disease, including but not limited to CKD stage 3 or greater
  11. history of ever meeting Diagnostic and Statistical Manual, version 5 (DSM-5) criteria for any schizophrenia spectrum disorder, bipolar spectrum disorder, major depressive disorder with psychotic features, or any other psychotic disorder, including substance-induced psychotic disorders ever in lifetime
  12. have a first or second-degree relative with history of schizophrenia spectrum disorder, bipolar spectrum disorder, major depressive disorder with psychotic features, or other psychotic disorder including substance-induced psychotic disorders ever in lifetime
  13. clinically significant suicide risk, as determined by clinician judgment and the C-SSRS. Participants will be excluded if any current active suicidal ideation, including intent to kill oneself or preparatory behavior, or a lifetime history of suicide attempts including aborted or interrupted.
  14. history within last 5 years of inpatient psychiatric hospitalization for any reason
  15. lifetime history of hallucinogen persisting perception disorder
  16. current or history within the last 1 year of meeting DSM-5 criteria for an alcohol or substance use disorder, excluding caffeine and nicotine; or a lifetime history of hallucinogen use disorder
  17. a positive urine drug screen or alcohol breathalyzer test result on any study visit, or unwillingness to provide these tests
  18. history of antisocial personality disorder, borderline personality disorder, or narcissistic personality disorder
  19. taking a primary psychoactive medication on a regular basis within 3 months of study participation, including but not limited to antidepressants (SSRIs, SNRIs, NDRIs, MAOIs, TCAs), antipsychotics, mood stabilizers, anxiolytics, stimulants, or sedative-hypnotics
  20. current clinically significant episode of any other psychiatric disorder, including but not limited to a current episode of major depressive disorder, anxiety disorder, trauma- or stressor-related disorder, obsessive-compulsive disorder, neurodevelopmental disorder, and personality disorder that is not in full remission
  21. any other current problem which, in the opinion of study clinicians, might pose an unacceptable risk to participant or staff safety and/or significantly interfere with study participation

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:基礎科学
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:トリプル

武器と介入

参加者グループ / アーム
介入・治療
実験的:Psilocybin
Psilocybin 25 mg oral capsule
1 dose of psilocybin 25 mg oral capsule
プラセボコンパレーター:Inert Placebo
Microcrystalline cellulose 25 mg oral capsule
1 dose of Microcrystalline Cellulose (MCC) 25 mg capsule

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Reinforcement Learning and Abstraction Task
時間枠:During dosing session and 1 day after the dosing session
Custom computer-based behavioral task requiring participants to complete a series of puzzles to complete game levels. This task requires working memory and reinforcement learning, and it also includes a measure of state abstraction.
During dosing session and 1 day after the dosing session
Belief Updating Task
時間枠:1 day before dosing, during dosing, and 1 day after the dosing session
Custom computer-based behavioral task in which participants must dynamically adjust predictions on each trial. This task measures trial to trial belief updating.
1 day before dosing, during dosing, and 1 day after the dosing session

二次結果の測定

結果測定
メジャーの説明
時間枠
Altered States of Consciousness Questionnaire (ASC)
時間枠:During dosing session
Measure of subjective experience.
During dosing session
Mystical Experience Questionnaire (MEQ)
時間枠:During dosing session
Measure of mystical type experiences
During dosing session
Psychological Insight Questionnaire (PIQ)
時間枠:During dosing session
Measure of psychological insight
During dosing session
Emotional Breakthrough Inventory (EBI)
時間枠:During dosing session
Measure of emotional breakthrough
During dosing session
Challenging Experience Questionnaire (CEQ)
時間枠:During dosing session
Measure of challenging subjective experiences
During dosing session
Warwick-Edinburgh Mental Wellbeing Scale (WEMWBS)
時間枠:1 day before dosing, 1 day after dosing, and 1 week after dosing
Measure of general wellbeing
1 day before dosing, 1 day after dosing, and 1 week after dosing
Clinician Administered Dissociative States Scale (CADSS)
時間枠:1 day before dosing, during dosing, 1 day after dosing, 3 days after dosing, and 1 week after dosing
Measure of dissociative experiences
1 day before dosing, during dosing, 1 day after dosing, 3 days after dosing, and 1 week after dosing
Barcelona Music Reward Questionnaire (BMRQ)
時間枠:From baseline to 1 week after dosing
Measure of music reward experiences
From baseline to 1 week after dosing
Geneva Emotional Music Scale, 9-item version (GEMS-9)
時間枠:During dosing session, 1 day after dosing
Measure of music experiences
During dosing session, 1 day after dosing
Modified Stanford Expectations of Treatment Scale (SETS)
時間枠:1 day before dosing session
Measure of expectancy about psychological changes from psilocybin
1 day before dosing session
Bang Blinding Index
時間枠:1 day after dosing
Measure of blinding integrity
1 day after dosing
Custom Rapport Questions
時間枠:1 day after dosing
Measure of rapport with study team
1 day after dosing
Subjective intensity and valence
時間枠:During dosing session
Periodic measurements of subjective intensity and valence
During dosing session
Subjective insight
時間枠:During dosing session
Participant-triggered measurements of subjective insight experiences
During dosing session
Semi-structured interviews
時間枠:1 day after dosing session
Brief semi-structured interviews exploring several pre-specified themes, including tolerability, changes in cognition, subjective insight experiences, experience of music, and other subjective experiences from the dosing session.
1 day after dosing session
Columbia Suicide Severity Rating Scale (C-SSRS)
時間枠:From baseline to 1 week after dosing
Measure of suicidal ideation during every study visit
From baseline to 1 week after dosing
Incidence of Adverse Events
時間枠:From baseline to 1 week follow up
Monitoring for adverse events, including misuse monitoring
From baseline to 1 week follow up
Feasibility and Acceptability
時間枠:From baseline to 1 week after dosing
Percentage of full study completion; percentage of tasks and questionnaires completed per participant; semi-structured interview questions to assess tolerability of the study procedures
From baseline to 1 week after dosing

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年11月1日

一次修了 (推定)

2027年11月1日

研究の完了 (推定)

2027年11月1日

試験登録日

最初に提出

2026年9月8日

QC基準を満たした最初の提出物

2026年9月8日

最初の投稿 (実際)

2026年9月14日

学習記録の更新

投稿された最後の更新 (実際)

2026年9月14日

QC基準を満たした最後の更新が送信されました

2026年9月8日

最終確認日

2026年8月1日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

未定

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

はい

米国FDA規制機器製品の研究

いいえ

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