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Frequently Asked Questions

What can I expect?

Every study is unique, and participation will look differently for each one. There are many different activities that may be part of your participation. Some may ask you fill out a simple survey or give a sample of your blood. Others may ask you to take a medication and visit with a counselor. You will learn what is expected of you during the informed consent process.

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What is the informed consent process?

Before you decide whether or not to participate, you will have a chance to talk with a member of the research team. This process of learning key facts about a study is called the informed consent process. The informed consent process continues during the entire time that you are part of the study. You should feel comfortable asking questions at any time.

You will also be given an informed consent document that describes the study and your role. It also explains that participation is voluntary and that you have the right to withdraw at any time. An "informed consent" is an informational document, not a contract.

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What questions should I ask?

If you have any questions about a study, make sure to speak up. Study coordinators, nurses, doctors and others involved in the research process are all willing to take the time to answer any questions you might have.

Be sure to ask questions when you are thinking about joining a research study, as well as any time during the study that you need more information. Some questions you might want to ask include:

  • Who is in charge of this study?
  • Do the people running the study have a vested interest (conflict of interest) in the outcome?
  • What is this study trying to find out?
  • What will be expected of you?
  • Is it possible that you might receive a placebo?
  • What benefits or risks can you expect if you take part in this study?
  • How long will the study last?
  • What happens if your condition gets worse during the study?
  • Can you continue seeing your own doctor during the study?
  • Will you need to pay for any part of the study, including doctor visits and routine tests?
  • Who pays if you're unexpectedly injured in the trial?
  • How will your participation in the study affect your daily life?
  • What happens at the end of the study?
  • Will you be told the results of the study? When?
  • Who will know that you're participating in the study?
  • How are trials conducted?
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Who do I call if I have a concern?

If you have questions while you are considering volunteering for research, or you are already a research volunteer with questions or concerns it is important to:

  • Talk with your research study team
  • Talk with your physician or care providers

If you have unanswered questions, concerns, or ideas for improving research practices, the Research Subject Advocate is available to assist you.

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