What actually happens at a screening visit

Consent first, then questions, then a few standard measurements. Here is the order things happen in, and what you can say no to.

A coordinator walking a participant through a screening visit

A screening visit is the first time you come to the site in person. It is not the study itself. It exists to answer one question for both sides: is this particular study a reasonable fit for you? You can decide it is not, at any point, and walk out.

Before anything else, the consent form

Nothing happens until you have read a consent form and signed it. Not a blood draw, not a questionnaire, not a memory test. The form describes what the study involves, how long it lasts, what is known about the risks, and what happens to your information.

Take it home first if you want to. Read it with someone. Bring it back with notes in the margin. A coordinator will go through it with you line by line and answer the same question as many times as you need to ask it. Signing it is not enrollment either — it is permission to find out whether you are eligible.

Your medical history and your medications

Bring a list of everything you take, including doses: prescriptions, over-the-counter medicines, vitamins and supplements. Photographing the labels on your phone works just as well as a written list.

This matters more than people expect. Many protocols exclude certain combinations, and a medication you did not think to mention is one of the most common reasons a screening visit has to be repeated.

The measurements

What gets measured depends entirely on the protocol. A typical visit may include some of the following:

  • Vital signs — blood pressure, heart rate, height and weight.
  • A blood draw and, in some studies, a urine sample.
  • An ECG, which records your heart rhythm through stickers on your chest.
  • Questionnaires about your symptoms and how you have been feeling.
  • Structured assessments — memory tasks, movement tasks or a headache history, depending on the area.

None of these are tests you can pass or fail. They establish a starting point. If something is out of range, that is information, not a verdict.

What you can decline

Any of it. You can decline a single procedure and continue, or decline the study altogether. You do not have to explain why, and it does not affect your regular medical care or your relationship with your own doctor.

Some procedures are required by the protocol, so declining one may mean the study is not workable for you. The coordinator will tell you plainly when that is the case rather than letting you find out later.

How long it takes

Plan for around two hours at our Stockbridge site, though it varies by protocol. Some studies ask you to arrive without having eaten; the coordinator will tell you in advance if that applies. Bring your glasses and hearing aids if you use them — several assessments depend on reading or hearing clearly.

Afterward

Some results come back the same day and some take longer. The coordinator will tell you when to expect an answer and will call you either way, including when the answer is that this study is not a fit. Not qualifying for one protocol says nothing about the next one.

This article explains how clinical research works in general. It is not medical advice, it does not describe any specific study, and it is no substitute for a conversation with your own doctor. Eligibility for any study at CRIGA is determined only after informed consent and screening.

Keep reading

Wondering whether a study could be a fit?

Answer a few questions and a study coordinator will call you back. No cost, no obligation, and nothing begins until you sign a consent form.

Start Pre-Screening