Patient-Driven Research Community Learning Network (PDRC LN)
In its strategic plan, the Patient-Centered Outcomes Research Institute (PCORI) articulated three goals for patient and stakeholder engagement in research:
developing a community skilled in patient-centered outcomes research
engaging the patient and stakeholder community in the research process
engaging the community in dissemination
To meet these goals, PCORI funded the Patient/Participant-Driven Research Community Learning Network (PDRC LN). A PDRC is defined as an organization or group of individuals or organizations that is led or governed by patients, participants, and caregivers. A PDRC’s primary purpose is to enable research that is a priority to the communities they serve.
NORC and our partner AcademyHealth led the PDRC LN, which launched in August 2019 with eight PPRN Engagement Awardees (PPRN EAs) and an aim to share and synthesize knowledge that would advance the role of PDRCs in clinical and care delivery research.
Learning network activities included monthly calls that served as a forum for the LN to share lessons and workshop challenges, bimonthly online seminars that brought in external experts, and annual virtual meetings of network members.
Additionally, NORC facilitated three workgroups related to key PDRC priorities around representativeness, sustainability, and digital engagement.
Finally, NORC conducted a landscape assessment, which included a review of peer-reviewed and gray literature on patient-driven research, identification and categorization of potential PDRCs in the field, and key informant interviews with different types of PDRCs. This project ended in January 2022.
Key deliverables from this project include:
The Value Proposition Playbook for Participant-Driven Research in Health Care (VPP) is an action-oriented, step-by-step roadmap that draws from current evidence and experience and contains a series of practical exercises designed to enable PDRCs to think about how they define their value and emerge with a plan to communicate their value proposition to potential partners.
The Patient Driven Research Community Research Activities Brief contains important lessons learned describing the functions and capacities of PDRCs in the health research landscape that could be a helpful tool for PDRCs to identify and articulate their value to potential research partners.
The Strategies for Improving Patient Representativeness in Research Governance Report examines the significance of and strategies for improving patient representativeness in research governance and provides examples of governance recruitment and retention practices sourced from literature scans and case study interviews.
The Digital Strategies for Returning Value to Research Participants Report examines principles for returning value to research participants and provides examples of digitally based engagement strategies sourced from literature scans and case study interviews.
Project Director
Related Tags
Project Leads
-
Prashila Dullabh
Vice President & Senior FellowProject Director -
Megan Skillman
Senior Research ScientistProject Manager and Research Co-Lead -
Gretchen Williams Torres
Associate DirectorNetwork Workgroups Co-Lead -
Petry S. Ubri
Senior Research ScientistResearch Lead -
Denise Bellows Kumar
Senior Research DirectorResearch and Dissemination Co-Lead
