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An Evaluation of Long-Term Supplement Use on Biological Age and Metabolic Health Markers - The BioAge Trial

Shaklee Corporation · with Biofortis Clinical Research, Inc., Nlumn LLC · NCT07755943

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 40+ · All sexes
Healthy volunteers
Accepted
Study type
Observational
Target enrollment
300
US sites recruiting
1
Study start
May 12, 2026
Record last updated
August 10, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

This study will evaluate whether dietary supplement use (> 1 year) is associated with differences in biological age relative to chronological age, as well as differences in metabolic health and functional fitness tests.

Being studied: No Intervention: Observational Cohort

Conditions: Generally Healthy Adults Who Are Long-term Supplement Users

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria

  • Adults aged 40 years or older.
  • Verified long-term Sponsor supplement use (>1 year).
  • Willing and able to provide informed consent and comply with study procedures.
  • Able to fast overnight (>8 hours) prior to the study visit.
  • Willing and able to travel to the test site.
  • Ambulatory and currently free of injury or other physical impairment that hinders mobility.
  • Willing to use a personal smart phone or computer with internet access and active email address.
  • Willing to adhere to all study procedures and sign forms providing informed consent to participate in the study and authorization to release relevant protected health information.

Exclusion Criteria

  • Current or recent (within 6 months) diagnosis of cancer except for non-melanoma skin cancer.
  • Participant is pregnant or lactating.
  • Participant has a pacemaker or other implanted electronic device.
  • Any condition the study staff believes would interfere with the participant's ability to provide informed consent or comply with the study protocol, which might confound the interpretation of the study results or put the person at undue risk.

Recruiting US locations

Study contacts (from the official record)

  • Biofortis Research Clinical Director · (630) 617-2000 · biofortisresearch@mxns.com
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An Evaluation of Long-Term Supplement Use on Biological Age and… (NCT07755943) | Bored Studies