This Knowledge to Action Guide from the Institute for Patient and Family-Centered Care provides guidance and best practices for creating partnerships with typically underrepresented patient, family, and community partners in research. The guide also offers strategies and insights, stories from the field, top tips, and selected resources to learn about, facilitate, and strengthen engagement of diverse patient, family, and community partners such that research can be co-designed and co-implemented.

Disclaimer: This tool was developed and provided by a third party. Opinions and information in this content are those of the third party and do not necessarily represent the views of PCORI. Accordingly, PCORI cannot make any guarantees with respect to the accuracy or reliability of the information and data in this content.