What is informed consent?

• Informed consent is a process in which you are given information about a clinical research study so that you can decide whether you want to participate.
• This information includes details about the study’s possible risks and benefits. This process is meant to help you decide whether participation in the study is right for you.
• You will receive an informed consent form that explains the study and gives you this information. Read the form carefully and ask any questions you may have about the study.
• If you agree to be in the study, you will need to sign the informed consent form to show that you understand the study and its possible risks and benefits.