Clinical Research

Interested in Clinical Research? Start Here.

If you’re curious about clinical trials — whether you heard about a study on the news, a family member mentioned research, or you’re wondering how a normal person even gets into a study — this page walks through the practical process. You don’t need research experience to start here.

You don’t necessarily need to know which trial you want

Clinical trials have specific eligibility criteria, and research sites help determine whether a particular study may be appropriate for you. You don’t need to arrive knowing exactly which trial you want — you need to arrive with enough information for the research team to assess whether you might fit.

Start with what you already know

Before contacting a research site, it helps to gather some basic information about your medical history and cognitive health:

  • Diagnosis, if you have one
  • Current symptoms and approximately when they began
  • Current medications (including over-the-counter and supplements)
  • Major medical conditions
  • Previous cognitive testing results
  • MRI or PET scan results, if available
  • Biomarker testing results, if performed
  • Relevant genetic testing results, if known (for example, APOE status)

You do not need to have all of these tests or results before contacting a research site. Gather what you have — the research team can help determine what else may be needed.

If you don’t have a diagnosis yet

You do not always need a final diagnosis before contacting a research site. Some studies recruit people with memory or thinking concerns, mild cognitive impairment (MCI), particular biomarkers or genetic risk factors, and some recruit people who are cognitively unimpaired.

Research participation is not a replacement for medical care, but screening for a clinical trial can sometimes provide access to testing that would otherwise be expensive or difficult to obtain.

Depending on the study, screening may include:

  • Cognitive testing
  • MRI
  • Amyloid PET or other PET imaging
  • Blood-based biomarkers such as phosphorylated tau
  • Laboratory testing
  • Genetic testing
  • Other specialized assessments

These tests are generally performed at no cost to the participant when they are required by the research protocol.

Whether individual results can be disclosed varies by the study, test, protocol, and research site. Ask: “Which of my screening or study results can be shared with me, and can I take those results to my healthcare provider?”

Cost can matter.

For someone facing high deductibles, limited insurance coverage, or a fixed income, access to study-related testing may be meaningful. It should not be the only reason to participate, but it is reasonable to ask a research site what testing is included and which results can be shared with you.

You may need a study partner

Many dementia and cognitive-impairment trials require participants to enroll with a study partner. The exact requirements vary by study.

Study partners are needed because:

  • They can provide information about changes in memory, thinking, behavior, and day-to-day function that the participant may not notice themselves.
  • Researchers may interview them or ask them to complete questionnaires or rating scales.
  • They can help the research team understand whether something has changed over time.
  • Depending on the study, they may help with appointments, medication or study-treatment logistics, and communication with the research team.

Who can be a study partner?

A study partner is often a spouse or partner, adult child, sibling, close friend, caregiver, or another person who knows the participant well. The study protocol determines the exact requirements. Generally, the person needs enough regular contact with the participant to reliably answer questions about their cognition and everyday functioning, and must be willing and able to participate in study-required visits, calls, or assessments. A study partner does not necessarily need to live with the participant unless a particular trial requires it.

Thinking about joining a dementia trial? Start thinking about your study partner early.

Before contacting a site, consider who knows you well, sees or speaks with you regularly, and would be willing to participate in study visits or interviews with you.

Where can you look?

ClinicalTrials.gov is the largest public database of clinical studies in the United States and internationally. You can search by condition, location, phase, and recruitment status. Each study listing includes a summary, eligibility criteria, and contact information for the research site.

Visit ClinicalTrials.gov

Explore the Alzheimer’s Research Pipeline

See treatments currently being studied for Alzheimer’s disease, organized by what they target and where they are in development.

Will I be paid to participate?

Some clinical trials compensate participants for their time and inconvenience. Some may also reimburse expenses such as mileage, transportation, meals, parking, or lodging. Amounts and policies vary considerably by study. Payment is not guaranteed — ask the site exactly what compensation and reimbursement are offered before enrolling.

What about taxes?

Payments for participating in medical research may be taxable income. Whether you receive a tax form depends on the amount and circumstances, and not receiving a tax form does not necessarily mean the income is not reportable. Expense reimbursements may be treated differently depending on the circumstances. Keep records of payments and reimbursements and ask the research site what tax documentation it provides. For questions about your own tax situation, consult a qualified tax professional.

What happens after you contact a research site?

1

Contact the site

You reach out to a research site listed on a study’s page — by phone, email, or online form.

2

Brief prescreen

A research coordinator asks basic questions about your diagnosis, symptoms, and medical history to see if you might fit the study.

3

Review basic eligibility

The site reviews your information against the study’s inclusion and exclusion criteria.

4

Screening visit / testing

If you appear to qualify, you’re invited for a screening visit, which may include cognitive testing, blood work, MRI, or other assessments.

5

Eligibility determination

The study team reviews screening results and determines whether you meet all eligibility criteria.

6

Informed consent / enrollment

If eligible, you review and sign the informed consent document, which explains the study, risks, and your rights. Enrollment then begins.

Contacting a site or completing a prescreen does not obligate you to participate and does not guarantee eligibility. You can withdraw at any point in the process.

Questions to ask before joining a study

These questions can help you understand what a study involves and whether it’s right for you. Tap each question to see why it matters.

Not sure what disease category fits?

If you’re not sure which condition applies to your situation, the “Understand what’s happening” pathway can help you work through cognitive changes, diagnosis, and testing — before exploring research.

Go to Start Here