Clinical trial Recruiting at 1 site Observational Ages 55 and up

Mapping body rhythms over time in older adults

Official title: An Observational, Longitudinal Study to Characterize the Dynamic Structure of Molecular and Digital Health Data in Healthy Older Adults

Run by Buck Institute for Research on Aging · NCT07107386 · Data updated 2026-11-12

This project will see how daily and weekly biological changes—from blood, urine, and wearable devices—track in healthy adults aged 55 and older.

Quick facts

Study typeObservational
Ages55 Years and up
SexAll
Enrollment120 (estimated)
SponsorBuck Institute for Research on Aging
Academic / other
Locations1 site (Novato, California)
StatusRecruiting
StartedJune 15, 2025
Main results expectedJune 2027
Study endsJune 2028
Registry record updatedAugust 15, 2025
Trial IDNCT07107386 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Healthy adults age 55 or older who live in the Pacific or Mountain Time zones, own a compatible smartphone, can speak English, and can travel to the Buck Institute in Novato, CA for weekly visits are ideal candidates.

Probably not a fit

People with recent hospitalization, unstable or serious chronic conditions, those on excluded medications or frequent antibiotics, night or irregular shift workers, non-English speakers, or those unable to attend weekly visits are unlikely to benefit or be eligible.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The TIME project follows healthy adults aged 55+ with weekly in-person visits over 11 weeks to collect blood, urine, and other biological samples. Participants wear health-tracking devices (such as a smart ring and smartwatch) and use smartphone apps so researchers can collect continuous physiological and behavioral data. Researchers will integrate molecular measurements with wearable and activity data to map short-term (daily and weekly) rhythms across multiple body systems. The goal is to better understand normal aging-related patterns and provide a foundation for more personalized timing of care and diagnostics.

Why it matters

Potential benefit: If successful, the findings could enable more personalized healthcare by timing treatments and monitoring to an individual's natural biological rhythms.

How similar studies have gone: Previous chronobiology and wearable-device studies have produced useful insights into daily rhythms, but this dense, multimodal weekly sampling approach in older adults is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Healthy adults aged 55 years or older.
* Own a smartphone capable of running study-specific apps.
* Willing and able to attend in-person visits at the Buck Institute in Novato, CA.
* Reside in the Pacific or Mountain Time Zones.
* Able to speak, read, and write English.
* Willing to wear study devices continuously and allow researchers access to all data.
* Able to provide informed consent.

Exclusion Criteria:

* Hospitalization within the last 3 months.
* Needing assistance with daily living activities.
* Working night or irregular shifts.
* Certain musculoskeletal, pulmonary, or cardiovascular conditions.
* Uncontrolled high blood pressure (BP \> 180/100 mmHg).
* Bleeding disorders, anemia requiring treatment, or recent blood donation.
* Poor vein access.
* Unstable health conditions.
* Chronic antibiotic use.
* Certain psychiatric disorders.
* Use of excluded medications, supplements, or products, including certain antibiotics or frequent sleep aids.

Where it's running

  • Buck Institute
    Novato, California, United States
    Recruiting

Study contacts

  • Principal investigator: James Yurkovich, PhD — Phenome Health, The Buck Institute for Research on Aging
  • Study coordinator: Brianna Stubbs, Research Assistant Professor, PhD.
  • Email: TIME-Study@buckinstitute.org
  • Phone: (415) 209-2072

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.