The study is open to participants who meet the following criteria:

• Male or female subjects 50 years of age or older
• Able to provide signed written informed consent
• Must be in general good health
• Must have had regenerative antiaging treatments in the past and are willing to provide information regarding those treatments
• Must plan on engaging in regenerative antiaging treatments in the future and are willing to provide information regarding those treatments
• Agrees to complete, under their personal physician’s care and provide to the investigator/s, 2 routine blood work panels per year, approximately 6-months apart, to include a complete blood count (CBC), a comprehensive metabolic panel (CMP), a lipid panel (LP) and a C-Reactive Protein (CRP) test
• Agrees to complete all study surveys according to the study schedule
• Agrees to conduct and report all study required physical measurements and functional tests according to the study schedule
• Agrees to provide past and future medical records to the research team for the duration of the study

The Assessing Regenerative Treatments study will last 10 years.

Your participation in the Assessing Regenerative Treatments study is critical to the advancement of our understanding of aging. To protect your health data and make it easier for you to participate, Vitality in Aging Research Group has built our research project on REDCap (research electronic data capture), a secure, encrypted, online research platform.

If you select the enroll button below the link will take you to the Assessing Regenerative Treatments study on REDCap. There you will be presented with several forms to complete.

• A registration form where you will provide your contact information
• A prescreening form where you will be asked several yes or no questions to see if you qualify to participate in the study
• An e-Consent form where you will receive more information about the study and if you choose, agree to participate in the study
• An intake form where you will provide more information about yourself and your health, much like the forms you fill out when first going to a new doctor

Once you have completed your informed consent and intake form, you will receive a copy by email of your signed consent for your records.

Then, once a month (for 10 months of the year), you will receive an automated notification by email, with a link to complete your monthly questionnaire and then twice a year (every six months), you will receive an automated notification by email, with a link to complete your biannual questionnaire.

You will also be asked to upload any blood test results and/or anti-aging regenerative treatment records you may have.

No. The Assessing Regenerative Treatments study is only enrolling citizens or residents of the United States.

Participating in the Assessing Regenerative Treatments study requires you provide and upload the results of your routine blood work twice a year (approximately every 6 months).

The blood tests include:

• complete blood count (CBC)
• comprehensive metabolic panel (CMP)
• lipid panel (LP)
• C-Reactive Protein (CRP) test

Most participants have these blood tests done through their healthcare provider (with or without insurance) or order the test through an online provider.

Typically, these routine blood tests are covered by insurance, however, please check with your healthcare provider.

No, you may get your blood test done at any lab, as long you complete the required tests:

• complete blood count (CBC)
• comprehensive metabolic panel (CMP)
• lipid panel (LP)
• C-Reactive Protein (CRP) test

The Assessing Regenerative Treatments study will use an automated virtual observational method to collect data. This means that the study will record your activities, behaviors, or other information you provide through our online platform, without any direct interaction from the research team.

Our team will be available to assist if a participant requires help with the use of these digital tools, however, you will not receive any feedback during the study. There will be no messages, comments, or responses from the research team about the study or its findings during the time the study is active.