- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07646782
Human Observatory Study (HOS)
The Human Observatory: A Prospective Individual and Population-Level Study of Aging, Health, and Longevity
Studieoversigt
Status
Betingelser
- Hjerte-kar-sygdomme
- Neoplasmer
- Dødelighed
- Erhvervssygdomme
- Kognitiv dysfunktion
- Metabolisk syndrom
- Demens
- Skrøbelighed
- Aldring
- Muskuloskeletal sygdom
- Dagliglivets aktiviteter
- Miljøeksponering
- Handicap Fysisk
- Sociale determinanter for sundhed
- Neurodegenerativ sygdom
- Sundhedsrelateret livskvalitet
- Sundhedslighed
- Dødelighed af alle årsager
- Life Expectancy
Intervention / Behandling
Detaljeret beskrivelse
Existing approaches to human health prediction face a structural limitation: individual clinical studies measure biology without capturing the environment, while population epidemiology captures the environment without individual biological ground truth. The Human Observatory Study resolves this by operating at both levels simultaneously through a linked dual-layer architecture.
At the individual level, participants enrolled in the 100-Year Human Aging Study contribute comprehensive multi-system health measurements. This includes clinical, physiological, cognitive, behavioral, social, occupational, and environmental data collected at fixed and mobile clinical sites. These measurements provide the biological present timepoint that historical population data alone cannot supply.
At the population level, the Observatory continuously ingests ecological data from public and private registries across multiple input domains. This includes air quality, water and chemical contaminants, wildfire and smoke exposure, altitude and terrain, climate, satellite earth observation, occupational and industrial exposure, mortality and vital statistics, demographics and social determinants, and clinical data networks at geographic resolutions from home address to global scale and beyond. This ecological layer captures the environmental and social causal structure of health and disease continuously and does not require individual enrollment.
A foundational input domain is genealogy and family history. Health and disease run in families across generations. The Observatory is designed to build and continuously expand a linked genealogical database connecting living and historical individuals to their family health histories. Information is obtained from public genealogical records, death registries, family history self-report, and genetic data where available. The long-term vision is a genealogical infrastructure of sufficient depth and breadth to trace familial health patterns across the full recorded human family tree. Therefore connecting individual present-timepoint biology to multigenerational patterns of disease, longevity, and environmental exposure that no existing biobank or longitudinal study has attempted to capture at this scale.
The linked architecture enables a feedback loop with two outputs: population-level causal estimates that inform individual screening recommendations, and individual clinical data that give population models a present biological anchor for prospective forecasting. The degree to which each input domain, alone and in combination, predicts health, disease, and death across geographic scales from neighborhood to global and beyond is the central scientific question the Observatory is designed to answer.
The Observatory launches in Colorado, chosen as the founding site for its exceptional natural variation in altitude, wildfire smoke corridors, mining and industrial chemical geographies, and frontier-to-urban socioeconomic gradient all within a compact, well-characterized geography with established academic research infrastructure. Colorado proves the model. The architecture then replicates geographically, with each new location enriching the world model for every other. The long-term vision is global coverage and beyond. Every geography will contribute its environmental, social, and biological signal to a world model that gets more accurate with every geography studied, every participant enrolled, every dataset ingested, and every causal analysis conducted.
Undersøgelsestype
Tilmelding (Anslået)
Kontakter og lokationer
Studiekontakt
- Navn: William Brandenburg, MD
- Telefonnummer: 13035010016
- E-mail: info@longevitymetrics.org
Studiesteder
-
-
Colorado
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Boulder, Colorado, Forenede Stater, 80301
- Rekruttering
- Longevity Metrics
-
Kontakt:
- William Brandenburg, MD
- Telefonnummer: 3035010016
- E-mail: info@longevitymetrics.org
-
Kontakt:
- E-mail: info@longevitymetrics.org
-
Ledende efterforsker:
- William Brandenburg, MD
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Prøveudtagningsmetode
Studiebefolkning
Beskrivelse
Inclusion Criteria:
- Enrolled in the 100-Year Human Aging Study at any fixed or mobile clinical site; OR completion of online health screener with provision of geographic anchor data and consent.
Exclusion Criteria:
- Age under 18 years (current protocol; pediatric amendment planned).
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Life Expectancy Estimates by Geography
Tidsramme: From enrollment until death, assessed periodically, up to 100 years
|
Continuously-updated life expectancy point estimates with credible intervals generated at individual, neighborhood, ZIP code, county, state, national, global, and beyond-earth scales using individual clinical data linked to population mortality records, environmental context, and ecological data.
|
From enrollment until death, assessed periodically, up to 100 years
|
|
Geographic Disease Cluster and Outbreak Detection
Tidsramme: From enrollment until death, assessed periodically, up to 100 years
|
Statistically anomalous concentrations of incident disease, mortality spikes, or shared symptom patterns at neighborhood and community resolution.
|
From enrollment until death, assessed periodically, up to 100 years
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Individual Screening Recommendation Accuracy
Tidsramme: From enrollment until death, assessed periodically, up to 100 years
|
Concordance between population-level causal estimates used to generate individualized screening recommendations and actual individual health outcomes at longitudinal follow-up, assessed periodically as outcomes accrue.
|
From enrollment until death, assessed periodically, up to 100 years
|
|
Causal Effect Estimates for Modifiable Exposures
Tidsramme: From enrollment until death, assessed periodically, up to 100 years
|
Estimated attributable life-years gained or lost per unit change in modifiable environmental, occupational, and social exposures.
|
From enrollment until death, assessed periodically, up to 100 years
|
|
Geographic Variation in Disability-Free Life Expectancy
Tidsramme: From enrollment until death, assessed periodically, up to 100 years
|
Disability-free life expectancy stratified by geography, ascertained via the functional independence and disability survey instrument used across all three associated protocols.
|
From enrollment until death, assessed periodically, up to 100 years
|
|
Health Equity Characterization
Tidsramme: From enrollment until death, assessed periodically, up to 100 years
|
Life expectancy gaps and chronic disease disparities stratified by geography, income, race and ethnicity, educational attainment, and rural-urban classification.
|
From enrollment until death, assessed periodically, up to 100 years
|
|
Human Tree of Life Growth
Tidsramme: From enrollment until death, assessed periodically, up to 100 years
|
Total participants linked to genealogical record; multigenerational depth achieved; proportion of enrolled participants with identified biological relatives in the registry; total historical individuals linked across all genealogical databases.
|
From enrollment until death, assessed periodically, up to 100 years
|
|
Population Biological Age Acceleration
Tidsramme: From enrollment until death, assessed periodically, up to 100 years
|
Mean difference between chronological age and biological age estimate for repeat-visit participants, stratified by geographic and demographic characteristics.
|
From enrollment until death, assessed periodically, up to 100 years
|
|
Multi-Domain Predictor Modeling
Tidsramme: From enrollment until death, assessed periodically, up to 100 years
|
Assessment of individual and composite clinical, biological, behavioral, environmental, social, occupational, genealogical, and geographic measurements as predictors of all-cause mortality, life expectancy, and incident serious disease at population scale; analyses evaluate which domains are independently predictive, which are redundant, and which combinations provide additive or synergistic predictive value.
|
From enrollment until death, assessed periodically, up to 100 years
|
|
Incident Serious Health Events and Chronic Disease
Tidsramme: From enrollment until death, assessed periodically, up to 100 years
|
New diagnosis of myocardial infarction, stroke, cancer, dementia, heart failure, atrial fibrillation, sepsis, venous thromboembolism, COPD, chronic hypoxia, major fracture, type 2 diabetes, hypertension, COPD, chronic kidney disease, metabolic syndrome, or osteoporosis ascertained via periodic follow-up contact and health data network linkage.
|
From enrollment until death, assessed periodically, up to 100 years
|
Samarbejdspartnere og efterforskere
Sponsor
Efterforskere
- Ledende efterforsker: William Brandenburg, MD, Longevity Metrics
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
- Kropssammensætning
- Befolkningssundhed
- Sundhedslighed
- Forebyggende medicin
- Familie historie
- lang levetid
- Sociale determinanter
- Forventede levealder
- Funktionelt fald
- biologisk aldring
- Healthspan
- Kardiopulmonal træningstest
- Slægtsforskning
- udsat
- kausal slutning
- Miljøsundhed
- Mortalitetsforudsigelse
- Biomarker Validation
- Centenarian
- Human Family Tree
- Neighborhood Health
- Geographic Health Disparities
- Space Medicine
- Aerospace Medicine
- World Model
Yderligere relevante MeSH-vilkår
- Hjernesygdomme
- Sygdomme i centralnervesystemet
- Sygdomme i nervesystemet
- Psykiske lidelser
- Patologiske processer
- Metaboliske sygdomme
- Neurokognitive lidelser
- Glukosemetabolismeforstyrrelser
- Kognitionsforstyrrelser
- Insulin resistens
- Hyperinsulinisme
- Patologiske tilstande, tegn og symptomer
- Ernæringsmæssige og metaboliske sygdomme
- Skrøbelighed
- Neoplasmer
- Kognitiv dysfunktion
- Hjerte-kar-sygdomme
- Metabolisk syndrom
- Muskuloskeletale sygdomme
- Demens
- Neurodegenerative sygdomme
- Erhvervssygdomme
Andre undersøgelses-id-numre
- Observatory
- IORG0012336; IRB00014601 (Anden identifikator: OHRP)
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
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Kliniske forsøg med Hjerte-kar-sygdomme
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Ottawa Hospital Research InstituteAfsluttetStress | Crisis Resource Management (CRM) færdigheder | Advanced Cardiovascular Life Support (ACLS) færdighederCanada