Glossary of Terms
Community-Based Research
Community-based research involves studying people within a community to learn more about diseases or conditions that affect people in the community. top![]()
Control Group
A control group is a group of individuals who do not have the condition or disease that is being studied. A control group is studied to compare individuals who have a particular disease or condition with individuals who do not have that disease or condition. top![]()
De-identification
De-identification is the process of removing information that could be used to identify you, such as your name and address, from a blood sample or information collected from you. Blood samples and information are always de-identified before they are given to researchers. top![]()
Diagnostic Tests
Diagnostic tests are medical tests used to determine what disease or condition a person may have. top![]()
Informed Consent
Informed consent is the process in which a person learns about a research study and then agrees voluntarily to take part or decides not to take part in the study. This process includes signing a form that describes what will happen if the person decides to take part in the study. top![]()
Institutional Review Board
An institutional review board or IRB is group of individuals who are responsible for protecting the rights, safety, and well-being of research participants. top![]()
Protocol
The protocol is a document that describes the purpose of a research study, the research study plan and why the study is important. top![]()
Repository
A repository is like a bank where information and samples are placed for safekeeping until they are needed. top![]()








