A single-center longitudinal study of the diagnosis clinical course risk factors causes and treatment of cognitive impairment in aging Alzheimer s disease (AD) and related disorders

Are you eligible to participate in this study?

You may be eligible for this study if you meet the following criteria:

  • Conditions:
    Alzheimer's Disease
  • Age: Between 18 Year(s) - 100 Year(s)
  • Gender: Male or Female
  • Other Inclusion Criteria:
    1. Participants who are minimum of 18 years of age and able to provide informed consent
    2. Those willing to undergo an MRI and phlebotomy for bloodwork
    3. Participants must be willing to consent to brain donation. (To note: *The brain donation requirement may be waived depending on scientific need as defined by the PI.)
    4. Must have a study partner
    5. Participants and study partners must be fluent in English or Spanish.
    6. Participants have normal cognition with and without subjective cognitive decline, MCI, or dementia from AD and ADRDs.

You may not be eligible for this study if the following are true:

    1. Major neurological disorders other than AD/ADRD
    2. Significant psychiatric history
    3. HIV/AIDS
    4. Advanced organ disease or failure
    5. Organ transplantation
    6. Clinically significant auto-immune or inflammatory disease
    7. Severe, uncontrolled endocrine disease
    8. A history of malignancy within the past 5 years
    9. Permanent pacemaker
    10. Surgical implants that preclude MRI studies
    11. Significant history of alcoholism or drug abuse
    12. Lack of study partner
    13. Lack of decisional capacity at time of initial visit



If you are registered as a volunteer, please log in to contact the study team/express interest in this study.

Contact the research team to learn more about this study.

By clicking "Contact Research Team", your contact information will be sent securely to the research staff associated with the study. You will also receive a copy of this email in your inbox, as well as other notifications to determine your participation status in the study.