The Patient Engagement Panel (PEP) is a dedicated group of individuals who advise on research and the way it involves and impacts patients and caregivers. PEP members share their lived experiences as patients, family members, caregivers, community members, and advocates to improve all aspects of research from development through dissemination to deliver conscientious, feasible, and sustainable outcomes for community health centers and the people they serve.
Since 2012, the PEP has actively provided input and consultation on various proposals, studies, and initiatives to guide research that improves health and health care through conscientious, effective person-centered, clinical, and policy approaches.
For additional engagement-related resources, please visit the PCORnet® Knowledge Repository, which hosts resources across data, research, and engagement domains from all eight PCORnet® CRNs.
For more information about the PEP, please contact us.
