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.
Talk to your doctor about the risks and benefits of taking part in a clinical research study.