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

2026년 9월 8일 업데이트: 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.

연구 개요

연구 유형

중재적

등록 (추정된)

24

단계

  • 1단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

    • Rhode Island
      • Providence, Rhode Island, 미국, 02903
        • Brown University School of Public Health
        • 연락하다:

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

예

설명

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

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 기초 과학
  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 삼루타

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Psilocybin
Psilocybin 25 mg oral capsule
1 dose of psilocybin 25 mg oral capsule
위약 비교기: Inert Placebo
Microcrystalline cellulose 25 mg oral capsule
1 dose of Microcrystalline Cellulose (MCC) 25 mg capsule

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Reinforcement Learning and Abstraction Task
기간: 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
기간: 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

2차 결과 측정

결과 측정
측정값 설명
기간
Altered States of Consciousness Questionnaire (ASC)
기간: During dosing session
Measure of subjective experience.
During dosing session
Mystical Experience Questionnaire (MEQ)
기간: During dosing session
Measure of mystical type experiences
During dosing session
Psychological Insight Questionnaire (PIQ)
기간: During dosing session
Measure of psychological insight
During dosing session
Emotional Breakthrough Inventory (EBI)
기간: During dosing session
Measure of emotional breakthrough
During dosing session
Challenging Experience Questionnaire (CEQ)
기간: During dosing session
Measure of challenging subjective experiences
During dosing session
Warwick-Edinburgh Mental Wellbeing Scale (WEMWBS)
기간: 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)
기간: 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)
기간: 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)
기간: 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)
기간: 1 day before dosing session
Measure of expectancy about psychological changes from psilocybin
1 day before dosing session
Bang Blinding Index
기간: 1 day after dosing
Measure of blinding integrity
1 day after dosing
Custom Rapport Questions
기간: 1 day after dosing
Measure of rapport with study team
1 day after dosing
Subjective intensity and valence
기간: During dosing session
Periodic measurements of subjective intensity and valence
During dosing session
Subjective insight
기간: During dosing session
Participant-triggered measurements of subjective insight experiences
During dosing session
Semi-structured interviews
기간: 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)
기간: 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
기간: From baseline to 1 week follow up
Monitoring for adverse events, including misuse monitoring
From baseline to 1 week follow up
Feasibility and Acceptability
기간: 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

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

간행물 및 유용한 링크

연구에 대한 정보 입력을 담당하는 사람이 자발적으로 이러한 간행물을 제공합니다. 이것은 연구와 관련된 모든 것에 관한 것일 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 11월 1일

기본 완료 (추정된)

2027년 11월 1일

연구 완료 (추정된)

2027년 11월 1일

연구 등록 날짜

최초 제출

2026년 9월 8일

QC 기준을 충족하는 최초 제출

2026년 9월 8일

처음 게시됨 (실제)

2026년 9월 14일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 9월 14일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 9월 8일

마지막으로 확인됨

2026년 8월 1일

추가 정보

이 연구와 관련된 용어

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

미정

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

예

미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

구독하다