Patient Recruitment & Retention

BRG recognizes that each clinical trial is unique and understands the need to adjust our recruitment methods in order to identify qualified research candidates. BRG’s database consists of a demographic population that represents the community in which we serve. In addition to its Database, BRG uses various recruitment methods to identify qualified study participants. (Eg. Physician referral, radio & TV advertising, local print advertisements, etc.)

BRG recognizes that through education and continued follow up with study participants, "Lost-to-Follow up" & withdrawal rates can be minimized. Our informed consent process is very detailed and complete. We conduct a thorough review of each page of the Informed Consent Form prior to enrolling study participants and encourage them to ask questions throughout the review.

The research staff is required to document all questions asked by the Study Participant(s) and the research staff’s response to each question. Our study physicians are available to answer study participant’s questions during the informed consent review. Participants are allowed ample opportunity during the process to ask questions, and to take their time in making a sound decision. Our goal is not to merely meet the industry’s standard, but exceed it.

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