A: Informed consent is the process of providing you with key information about a research study before you decide whether to participate. To help you decide whether to take part, members of the research team will explain the details of the study. If you do not understand English, a translator or interpreter may be provided. During the informed consent process, the study team, including the physician overseeing the trial will discuss with you the risks and benefits associated with being a volunteer. They will share with you details about the study such as known safety information, the purpose of the trial, how long it is expected to last, any tests or procedures that will be done along with the expectations for you as a participant.
You can then decide whether to sign the document. Included on the informed consent form is contact information if you have any further questions, but we hope your clinical trial team will be able to answer them all for you. It is important to know that participating in a clinical trial is always voluntary, and you may leave the study at any time.