Psilocybin Effects on Healthy Aging Biomarkers and Purpose in Life (LONG-LIFE)
An Examination of Psilocybin Effects on Biomarkers of Longevity, Healthy Aging, and Purpose in Life
The LONG-LIFE study is a randomized Phase I, dose-ranging trial designed to evaluate whether psilocybin impacts aging-related biomarkers, cognitive function, and purpose/meaning in life in medically stable older adults.
Up to 50 participants will be enrolled aged 60-80 who will be randomized with equal allocation to one of four intervention groups: (1) receipt of one 25 mg dose of psilocybin; (2) receipt of two 25 mg doses of psilocybin separated by four weeks; (3) receipt of three 25 mg doses, with each dose separated by four weeks; or (4) wait-list comparator condition that does not receive psilocybin. Biomarkers of aging, cognitive performance, and behavioral measures will be assessed at baseline and longitudinally over a 12-month follow-up period. The primary endpoint occurs at the Week 16 visit. Participants randomized to the wait-list condition will be offered a single 25 mg dose of psilocybin following conclusion of the 12-month follow-up period.
Findings from this Phase I study will inform dose selection for a Phase II study should results indicate a potential impact of psilocybin on relevant study endpoints.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
Aging is accompanied by progressive changes across multiple physiological systems that contribute to functional decline and increased risk for age-related disease. Biomarkers of biological aging, including DNA methylation-based epigenetic clocks, have emerged as tools for assessing age-related biological processes and predicting future health outcomes.
Recent preclinical studies have suggested that psilocybin and its active metabolite, psilocin, may influence several pathways implicated in aging, including cellular senescence, oxidative stress, neuroplasticity, and epigenetic regulation. In addition to biological effects, observational studies have demonstrated associations between psychosocial factors, including purpose in life and social connectedness, and reduced morbidity and mortality in older adults. Previous clinical studies have shown that psilocybin may produce changes in psychological well-being, meaning, and related constructs.
The LONG-LIFE Study is designed to evaluate multiple domains relevant to healthy aging, including, but not limited to, epigenetic and biological clock measures, cognitive performance, psychosocial well-being, and ecological momentary assessments of daily experience.
Tipo de estudio
Inscripción (Estimado)
Fase
- Fase 1
Contactos y Ubicaciones
Estudio Contacto
- Nombre: BHIC Study Team
- Número de teléfono: 970-855-7374
- Correo electrónico: bhic@vailhealth.org
Ubicaciones de estudio
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Colorado
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Edwards, Colorado, Estados Unidos, 81632
- Vail Health Behavioral Health
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- English speaking and able to provide informed consent and complete study procedures
- Medically healthy, as determined by the screening physician, with no significant medical conditions that would interfere with participation or affect the safety of the subject.
Exclusion Criteria:
- History or presence of any psychiatric or medical condition that, in the opinion of the investigator, could pose a safety risk, interfere with participation, or confound study results.
- Abnormal ECG at screening that may increase risk during participation (e.g., prolonged QTc, arrhythmias, or other clinically significant findings as determined by the study physician).
- Unwilling or unable to discontinue medications that may interfere with study participation, as determined by the investigator.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Otro
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Doble
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Experimental: One 25mg Dose of Psilocybin
Participants in this arm will receive one 25mg dose of psilocybin paired with therapeutic support.
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25mg capsule of psilocybin
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Experimental: Two 25mg Doses of Psilocybin
Participants in this arm will receive two 25mg doses of psilocybin approximately 4 weeks apart paired with therapeutic support.
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25mg capsule of psilocybin
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Experimental: Three 25mg Doses of Psilocybin
Participants in this arm will receive three 25mg doses of psilocybin approximately 4 weeks apart paired with therapeutic support.
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25mg capsule of psilocybin
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Sin intervención: Wait-list Comparator
Participants in this arm will not receive psilocybin as part of the main study but will be given the opportunity to receive a single 25mg dose of psilocybin with therapeutic support after their study participation is complete.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Change in Epigenetic/Biological Clock Profiling from Baseline to Week 4 and Week 16
Periodo de tiempo: Change from Baseline to Week 4 and Week 16
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Epigenetic/biological clock profiles; change from Baseline to Week 4 and 16
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Change from Baseline to Week 4 and Week 16
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Change in Purpose in Life (PIL) from Baseline to Week 4 and Week 16
Periodo de tiempo: Change from Baseline to Week 4 and Week 16
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Change from baseline in Purpose in Life score measured using the 7-item Purpose in Life Scale (PIL) from the Health and Retirement Study (score range 1-6; higher scores indicate greater purpose in life).
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Change from Baseline to Week 4 and Week 16
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Change in Epigenetic/Biological Clock Profiling from Baseline to Week 52
Periodo de tiempo: Change from Baseline to Week 52
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Change in Epigenetic/biological clock profile from Baseline to Week 52
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Change from Baseline to Week 52
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Change in Telomere Length from Baseline to Week 52
Periodo de tiempo: Change from Baseline to Week 52
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Change from Baseline to Week 52
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Change in Purpose in Life (PIL) from Baseline to Week 52
Periodo de tiempo: Change from Baseline to Week 52
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Change from baseline in Purpose in Life score measured using the 7-item Purpose in Life Scale (PIL) from the Health and Retirement Study (score range 1-6; higher scores indicate greater purpose in life).
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Change from Baseline to Week 52
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Change in Satisfaction with Life from Baseline to Week 4 and Week 16
Periodo de tiempo: Change from Baseline to Week 4 and Week 16
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Measured using the Satisfaction With Life Scale (SWLS).
Scores range from 5 to 35, where higher scores indicate greater satisfaction with life.
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Change from Baseline to Week 4 and Week 16
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Change in Wellbeing from Baseline to Week 4 and Week 16
Periodo de tiempo: Change from Baseline to Week 4 and Week 16
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Measured using the Warwick Edinburgh Mental Well-Being Scale (WEMWBS).
Scores range from 14 to 70, with higher scores indicating higher mental wellbeing.
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Change from Baseline to Week 4 and Week 16
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Change in Optimism from Baseline to Week 4 and Week 16
Periodo de tiempo: Change from Baseline to Week 4 and Week 16
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Measured using the Life Orientation Test - Revised (LOT-R).
Scores range from 0 to 24, with higher scores indicating higher dispositional optimism.
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Change from Baseline to Week 4 and Week 16
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Change in Perceived Control/Mastery from Baseline to Week 4 and Week 16
Periodo de tiempo: Change from Baseline to Week 4 and Week 16
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Measured using the Pearlin Mastery Scale (PM).
Scores range from 7 to 28; higher totals indicate greater self-mastery.
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Change from Baseline to Week 4 and Week 16
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Change in Loneliness from Baseline to Week 4 and Week 16
Periodo de tiempo: Change from Baseline to Week 4 and Week 16
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Measured using the 3-Item UCLA Loneliness Scale (UCLA-3).
Scores range from 3 to 9. Higher scores indicate a greater degree of loneliness.
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Change from Baseline to Week 4 and Week 16
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Colaboradores e Investigadores
Publicaciones y enlaces útiles
Enlaces Útiles
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 20262840
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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