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NCT07755943 · Shaklee Corporation

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

What this 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.

View original scientific description

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.

Interventions

OTHER

No Intervention: Observational Cohort

No intervention: observational cohort

Primary outcome measures

Difference between biological and chronological age (years) calculated using a validated biological age calculator

Time frame: Baseline single assessment for this observational study

Differences will be compared to an NHANES cohort, where possible.

Who can participate

This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.

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.

Where

  • Addison, Illinois

Collaborators

Biofortis Clinical Research, Inc., Nlumn LLC

Related conditions & keywords

Generally Healthy Adults Who Are Long-term Supplement Users

Frequently asked questions

What is a clinical trial?

A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.

Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.

Will I be compensated?

Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.

Will I receive a placebo instead of treatment?

When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.

Can I leave a trial if I change my mind?

Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.

How long does a clinical trial last?

Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.

Data: ClinicalTrials.gov · synced Aug 10, 2026 · Source of record for eligibility and locations

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1 of 300 participants interested
0% interest

See if this study fits

A short prescreen based on this study's listed criteria. A coordinator confirms eligibility — this is not a medical assessment.

Preparing your pre-screening questions…

Study locations

Choose your preferred location, or select flexible during enrollment.

RECRUITING

Addison

Illinois

Location available

Express your interest

Share your contact details and a study coordinator can follow up about screening.

Secure & Confidential

Your information is protected and will only be shared with the research team.

What participation can include

  • Study-related care provided by the research team
  • Close monitoring by medical professionals
  • Possible compensation for time and travel*
  • The option to withdraw at any time
  • Contributing to medical research that may help future patients

*Compensation varies by study. Confirm details with coordinator.

Typical next steps

  1. 1.Submit this form
  2. 2.Phone screening
  3. 3.In-person assessment if eligible
  4. 4.Begin participation

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Looking for Generally Healthy Adults Who Are Long-term Supplement Users Treatment in Addison?

Join others in Illinois exploring innovative treatment options through clinical research

Generally Healthy Adults Who Are Long-term Supplement Users Treatment Options in Addison, Illinois

If you're searching for Generally Healthy Adults Who Are Long-term Supplement Users treatment in Addison, participating in a clinical research study may provide access to innovative approaches under expert medical supervision. This study is actively recruiting participants in Addison and surrounding areas.

Clinical trials offer participants the opportunity to receive cutting-edge treatments while contributing to medical research that may help future patients with Generally Healthy Adults Who Are Long-term Supplement Users. All study-related care is provided at no cost to participants.

Local Sites
1 locations in Illinois
Now Enrolling
Up to 300 participants
Quick Start
Screening available now

Why Consider a Clinical Trial for Generally Healthy Adults Who Are Long-term Supplement Users?

Potential Benefits

  • Access to new treatment approaches before public availability
  • Close monitoring by experienced medical professionals
  • Study-related care provided at no cost
  • Contribute to medical research for Generally Healthy Adults Who Are Long-term Supplement Users

What to Expect

  • Initial screening to determine eligibility
  • Regular check-ups and monitoring visits
  • Possible compensation for time and travel
  • You can withdraw at any time

Frequently Asked Questions About This Generally Healthy Adults Who Are Long-term Supplement Users Study

Important Clinical Trial Information

This information is provided for educational purposes and does not constitute medical advice. Clinical trial participation involves potential risks and benefits. Eligibility requirements apply and will be assessed during the screening process.

Study identifier: NCT07755943. For complete study details, visit ClinicalTrials.gov. Always consult with your healthcare provider before making decisions about your medical care or participating in clinical research.