Longevity Metrics AI/ML Development Study
1 other identifier
observational
1,000,000
1 country
1
Brief Summary
This study builds AI models that score diagnostic screening tests, and that predict screening results, clinical judgment, and life expectancy. Longevity Metrics collects a battery of clinical tests on each participant, in whole or in part, and follows every participant for life. The sit-to-rise test and the timed walk are scored by hand today, from a person's count. A model scores the same test from video instead. It also measures what no one can count by eye - speed, asymmetry, steadiness - so one capture yields both the original score and additional measurements, intended to enrich the model and strengthen what it predicts. Every test in a participant's record measures the same body, so the tests are correlated: a test that was performed carries information about one that was not. A model trained across the library learns those relationships and estimates a missing result from the results that are present. Each estimate is checked against records where that part was actually measured, and over decades against death and disease through linkage to the 100-Year Human Aging Study (NCT07563777). The hypothesis is that the full battery can eventually be predicted across modalities with high accuracy using a few short video clips, replacing most in-person screening. That would let preventive screening reach people and places a physical laboratory cannot. How far the input can be reduced is the question this study exists to answer. Every model is a physician-reviewed clinical decision aid until it is cleared by the FDA.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Aug 2026
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 8, 2026
CompletedFirst Submitted
Initial submission to the registry
September 2, 2026
CompletedFirst Posted
Study publicly available on registry
September 9, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2099
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2099
September 9, 2026
September 1, 2026
73.4 years
September 2, 2026
September 2, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (5)
Measurement Accuracy, Non-Inferiority to Human Scoring.
Agreement between the model's value and the reference standard, established as non-inferiority to a qualified human scorer where a human reference exists. Gates deployment as a clinical decision aid.
At each model freeze, through study completion, up to 100 years.
Cross-Prediction of Non-Performed Results and Derived Scores
Accuracy of predicting, from video or from the performed part of a record, both the screening results the participant did not obtain, against the measured value; and the derived scores computed from a complete record, including the Longevity Score, biological age, and estimated age at death, against the value the scoring engine produces from the full measured record.
At each model freeze, through study completion, up to 100 years.
Prediction of Remaining Life Expectancy
Accuracy of predicting remaining life expectancy from video and library data, against observed mortality through linkage to the 100-Year Human Aging Study.
Through study completion, up to 100 years
Prediction of Physician Clinical Judgment
Accuracy of predicting the physician's clinical judgment where no determining measurement exists, against the sealed record. Applies to models that predict a clinical determination rather than a measured value. Where a determining test exists but was not performed, the outcome falls under Primary Outcome 2.
At each model freeze, through study completion, up to 100 years
Screening-Related Injuries and Adverse Events
Participant injuries or adverse events attributed to measurements added under this study, such as the sit-to-rise test. Ascertained from two independent sources so that an event missed by one is still captured: the tester logs any fall or injury at the time of screening, and the participant reports separately on the post-screening form.
Continuously from first screening through study completion, up to 100 years
Secondary Outcomes (13)
Measurement Accuracy, Superiority to Human Scoring
At each model freeze, through study completion, up to 100 years
Uncertainty Calibration
At each model freeze, through study completion, up to 100 years
Within-Session Repeatability
At each model freeze, through study completion, up to 100 years.
Missing-Data and Completeness Robustness
At each model freeze, through study completion, up to 100 years
Physician Assessment of Model Output
Continuously from first model read through study completion, up to 100 years
- +8 more secondary outcomes
Interventions
Video and audio-captured physical, cognitive, and observational screening tests scored by frozen, versioned AI models; models automatically score standard tests (sit-to-rise, timed walk, chair stand), predict non-performed results from performed ones, and predict clinical judgment; all outputs are physician-reviewed clinical decision aids, and no model output reaches a participant report without provider confirmation.
Eligibility Criteria
Participants enrolled in the 100-Year Human Aging Study (NCT07563777) through the unified consent, receiving any Longevity Metrics health screening service at any fixed, mobile, or remote (online) site, current and future. Participants are self-selected community members of all health statuses; no exclusions based on health status, diagnosis, or population group. This study adds no separate enrollment: all records analyzed and all prospective measurements collected under this protocol arise from participants consented under the associated protocols. Participants are followed for life, with mortality, incident disease, and functional-status outcomes ascertained through linkage to the 100-Year Human Aging Study.
You may qualify if:
- Age \>= 18
- willing to participate in the study
You may not qualify if:
- Age \< 18 years
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Longevity Metrics
Boulder, Colorado, 80301, United States
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
William E Brandenburg, MD
Longevity Metrics, Inc.
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- OTHER
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 2, 2026
First Posted
September 9, 2026
Study Start
August 8, 2026
Primary Completion (Estimated)
December 31, 2099
Study Completion (Estimated)
December 31, 2099
Last Updated
September 9, 2026
Record last verified: 2026-09
Data Sharing
- IPD Sharing
- Will not share
Individual participant data are not shared. The complete participant record includes facial and voice recordings, genomic data, and neighborhood-resolution geography, and cannot be de-identified; it is never released. Identifiable data are accessed only by approved researchers working within Longevity Metrics secure facilities under data use agreements, with no data removed. Specific derived, aggregate, and statistical outputs are de-identified to HIPAA Safe Harbor standards and may be published, shared with collaborators, or contributed to open-access research databases. Models, risk estimates, and analytic findings derived from the research data may be provided to external organizations or used commercially; no participant record and no dataset containing participant data is transferred.