Psilocybin-Assisted Therapy as a Treatment for Depression
A Pilot Mechanistic Study of Psilocybin-Assisted Therapy as a Treatment for Depression
Depression is the leading cause of disability worldwide, affecting an estimated 300 million people. Despite available treatments, response rates remain modest, and treatment resistance is common. Novel treatments are needed that act rapidly, produce lasting effects and work differently than existing antidepressants.
In clinical trials, psilocybin has shown promise as a treatment for depression due to its rapid onset of antidepressant effects and sustained benefits.
This study will use MRI scanning of the brain and other biological measures (biomarkers) to investigate how psilocybin affects brain activity and psychological flexibility before, during, and after receiving psilocybin in participants with depressive symptoms.
調査の概要
研究の種類
入学 (推定)
段階
- フェーズ2
連絡先と場所
研究連絡先
- 名前:Dawnita Reathaford
- 電話番号:314-532-5939
- メール:dawnita@wustl.edu
研究場所
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Missouri
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St Louis、Missouri、アメリカ、63110
- Washington University School of Medicine
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コンタクト:
- Teddi Gray
- 電話番号:314-747-1862
- メール:grayt@wustl.edu
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コンタクト:
- Dawnita Reathaford
- 電話番号:314-362-5939
- メール:dawnita@wustl.edu
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参加基準
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
説明
Inclusion Criteria:
- Age > 18 years
- Participants of childbearing potential must agree to practice 2 forms of effective birth control throughout the duration of the study
- Females of childbearing potential must have a negative urine pregnancy test at Screening and prior to dosing on Dosing Day
- Diagnosis of depression at Screening via the SCID-5-CT interview and MADRS score of ≥7
- Have an identified support person Agree to be accompanied home (or to an otherwise safe destination) by the support person, or another responsible party, following dosing
Exclusion Criteria:
- Unable to read or understand English
- Is currently pregnant or breastfeeding, or plan to become pregnant or breastfeed within the study period
Has had Electroconvulsive Therapy, Transmagnetic Stimulation, Vagus Nerve Stimulation or Deep Brain Stimulation treatment within the last 12 months
a. Participants with VNS or DBS devices in place- including devices that are inactive or turned off will not be eligible to participate in the imaging portion of the study
Is currently taking a medication on the prohibited medications list, such as heterocyclic (tricyclic, tetracyclic) antidepressants, monoamine oxidase inhibitors (MAOIs), antipsychotic augmentation therapy, or is taking more than one medication for the treatment of depression:
- Participants who are taking a single prescription medication for depression must be on a stable, minimally therapeutic/tolerated dose for at least 4 weeks prior to Screening.
- Psychostimulants for the treatment of attention-deficit/hyperactivity disorder (ADHD) are allowed, if used at a stable dose or pattern for at least 6-weeks prior to Screening and not used on Dosing Day(s).
- Has a primary psychotic disorder diagnosis
- Has a first-degree relative with a known history of a psychotic disorder
- Meets criteria for substance use disorder or diagnosis of substance use disorder within 6 months prior to Screening
- Has an unstable medical condition or serious abnormalities of complete blood count, chemistries, or ECG, or taking medications that in the opinion of the study clinician would preclude safe participation in the trial
Is at risk for hypertensive crisis defined as:
- BP at Screening AND Baseline >140/90 mmHG
- BP on Dosing Day prior to dosing >140/90 mmHG
- Has used a serotonergic hallucinogenic substance (e.g., psilocybin, lysergic acid diethylamide (LSD), mescaline, N,N-dimethyltryptamine (DMT), 5-methoxy-N,N-dimethyltryptamine (5-MeO-DMT), ibogaine, 3,4-methylenedioxymethamphetamine (MDMA), or other related substances) within 6 months of Screening.
- Has a known sensitivity to psychedelic medications
- Has a positive urine drug test including amphetamines, barbiturates, buprenorphine, benzodiazepines, cocaine, methamphetamine (unless prescribed), MDMA, methadone, opiates, and phencyclidine (PCP)
- Is at high risk for suicide (e.g., active suicidal ideation and or current intent or plan) and unable to be managed safely (i.e., unwilling to be hospitalized)
研究計画
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:なし
- 介入モデル:単一グループの割り当て
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
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実験的:25mg Open Label dose of synthetic psilocybin
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Capsule containing 25 mg of synthetic psilocybin
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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 |
|---|---|---|
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Characterize ACUTE (~1 week post-dose) and PERSISTING (~30 days post-dose) effects of PAT in depressed adults at two possible administrations on depression symptom severity using the Montgomery-Asberg Depression Rating Scale (MADRS) score.
時間枠:1 week and 30 days post-dose for both administration sessions
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The MADRS is a 10-item instrument used to assess depression severity.
The total MADRS score ranges from 0-60, with higher scores indicating increased severity of depression
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1 week and 30 days post-dose for both administration sessions
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Characterize ACUTE (~1 week post-dose) and PERSISTING (~30 days post-dose) effects of PAT in depressed adults at two possible administrations on psychological flexibility using the Multidimensional Psychological Flexibility Inventory (MPFI).
時間枠:1 week and 30 days post-dose for both administration sessions
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The Multidimensional Psychological Flexibility Inventory (MPFI) is scored by averaging 60 items (or 24 in the short form) on a 1-6 scale (1 = "never true", 6 = "always true").
Higher average scores (1-6) indicate higher levels of the trait, with 12 subscales mapping onto psychological flexibility and inflexibility, allowing for detailed, sub-process, or global profiling.
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1 week and 30 days post-dose for both administration sessions
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協力者と研究者
出版物と役立つリンク
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
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