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Psilocybin Effects on Healthy Aging Biomarkers and Purpose in Life

An Examination of Psilocybin Effects on Biomarkers of Longevity, Healthy Aging, and Purpose in Life

Status
Not yet recruiting
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07719088
Acronym
LONG-LIFE
Enrollment
50
Registered
2026-07-22
Start date
2026-12-01
Completion date
2028-12-01
Last updated
2026-10-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aging, Longevity, Biomarkers of Aging

Keywords

Aging, Longevity, Cognitive Function, Purpose, Meaning, Well-Being, Biomarkers

Brief summary

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.

Detailed description

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.

Interventions

25mg capsule of psilocybin

Sponsors

Charles Raison
Lead SponsorOTHER
Baylor College of Medicine
CollaboratorOTHER
Steadman Philippon Research Institute
CollaboratorOTHER
Emory University
CollaboratorOTHER
University of Wisconsin, Madison
CollaboratorOTHER
Usona Institute
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
60 Years to 80 Years
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
Change in Epigenetic/Biological Clock Profiling from Baseline to Week 4 and Week 16Change from Baseline to Week 4 and Week 16Epigenetic/biological clock profiles; change from Baseline to Week 4 and 16
Change in Purpose in Life (PIL) from Baseline to Week 4 and Week 16Change from Baseline to Week 4 and Week 16Change 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).

Secondary

MeasureTime frameDescription
Change in Epigenetic/Biological Clock Profiling from Baseline to Week 52Change from Baseline to Week 52Change in Epigenetic/biological clock profile from Baseline to Week 52
Change in Telomere Length from Baseline to Week 52Change from Baseline to Week 52—
Change in Purpose in Life (PIL) from Baseline to Week 52Change from Baseline to Week 52Change 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).
Change in Satisfaction with Life from Baseline to Week 4 and Week 16Change from Baseline to Week 4 and Week 16Measured using the Satisfaction With Life Scale (SWLS). Scores range from 5 to 35, where higher scores indicate greater satisfaction with life.
Change in Wellbeing from Baseline to Week 4 and Week 16Change from Baseline to Week 4 and Week 16Measured using the Warwick Edinburgh Mental Well-Being Scale (WEMWBS). Scores range from 14 to 70, with higher scores indicating higher mental wellbeing.
Change in Optimism from Baseline to Week 4 and Week 16Change from Baseline to Week 4 and Week 16Measured using the Life Orientation Test - Revised (LOT-R). Scores range from 0 to 24, with higher scores indicating higher dispositional optimism.
Change in Perceived Control/Mastery from Baseline to Week 4 and Week 16Change from Baseline to Week 4 and Week 16Measured using the Pearlin Mastery Scale (PM). Scores range from 7 to 28; higher totals indicate greater self-mastery.
Change in Loneliness from Baseline to Week 4 and Week 16Change from Baseline to Week 4 and Week 16Measured using the 3-Item UCLA Loneliness Scale (UCLA-3). Scores range from 3 to 9. Higher scores indicate a greater degree of loneliness.

Countries

United States

Contacts

CONTACTBHIC Study Team
bhic@vailhealth.org970-855-7374

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Oct 14, 2026