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DC Longitudinal Study on Aging and Specimen Bank

Study on aging and specimen collection in DC.

Recruiting
45 years and older
All
Phase N/A

The Georgetown University Memory Disorders Program is studying how to diagnose Alzheimer's and other brain-related diseases before they cause major damage. They use tests on blood or cerebrospinal fluid (CSF), which is a liquid around your brain and spine. The study also looks at how lifestyle and genetics affect these diseases.

Participants can join one of two parts of the study. The "main study" involves one visit to the clinic for some cognitive tests and to provide blood or CSF samples. The "longitudinal sub-study" requires more visits. If you're in the cognitively normal group, you'll visit every other year, with phone check-ups in between. If you have mild cognitive impairment (MCI) or Alzheimer's, you'll visit every year.

Key Points:
  • Initial visit includes cognitive tests and sample collection.
  • Longitudinal study involves yearly or bi-yearly follow-ups.
  • Participants must be 45 or older; those 45-50 need a family history of these diseases.

No personal test results will be shared. This research helps improve future diagnoses and treatments.

Study details
    Alzheimer Disease
    Dementia
    Mild Cognitive Impairment
    Aging
    Aging Disorder

NCT03702907

Georgetown University

17 April 2026

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Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

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The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

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Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

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Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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