What We Can Do for You

Informed consent is the process of learning the key facts about a clinical trial before deciding whether or not to participate. It is also a continuing process throughout the study to provide information for participants. To help someone decide whether or not to participate, the doctors and nurses... Read More

We provide a information for participants on what questions to ask and what our advocates can do for you. For more information, please see the Participant Advocate Program brochure. Read More

A research participant is someone who participates in a research study. Research involving human participants (often referred to as 'subjects') may take place in many places in and around the community. The majority of GHUCCTS-related research will take place in the Washington, DC metro area at... Read More

Please click on the Rights & Responsibilities for a list.  Read More

Our research subject advocates help ensure the rights, safety, and well-being of participants in GHUCCTS-supported research studies. Research subject advocates enhance the standard protections available for participants in clinical research through advocacy for study participants, through... Read More