PCORI Awards $9 Million Contract to Harvard Group to Coordinate National Patient-Centered Clinical Research Network
Consortium will help build a robust network for conducting comparative effectiveness research
WASHINGTON, Sept. 11, 2013 /PRNewswire-USNewswire/ — The Patient-Centered Outcomes Research Institute (PCORI) Board of Governors today selected a consortium led by the Harvard Pilgrim Health Care Institute to serve as the Coordinating Center for a new national data network designed to enhance the nation’s ability to conduct patient-centered comparative effectiveness research (CER).
The $9 million Harvard Pilgrim proposal, approved during a special Board webinar/teleconference, was one of eight PCORI received in response to a June Request for Proposals. All were assessed based on scientific and technical merit and detailed cost analyses and three finalists were interviewed by PCORI staff. Harvard Pilgrim was judged to have the strongest proposal.
The Coordinating Center will provide technical and logistical support to the proposed new National Patient-Centered Clinical Research Network. The initiative’s goal is to improve the nation’s capacity to conduct CER efficiently and learn from the healthcare experiences of millions of Americans by creating a large network of health data representative of patients from across the country.
PCORI committed $68 million in April to develop the national data network through the creation or expansion of up to eight health system-based Clinical Data Research Networks (CDRNs) and up to 18 Patient-Powered Research Networks (PPRNs) organized by groups of patients interested in participating in clinical research. Groups invited to submit proposals through the institute’s competitive application process have until Friday, Sept. 27, to submit them. Awardees will be announced in December.
The Coordinating Center will assist the CDRNs and PPRNs with technical and logistical support and play a critical role in fostering communication and coordination among them as well as disseminating best practices. It will also support program evaluation.
“We had several compelling proposals to consider but in the end, the Harvard Pilgrim team’s proposal stood out as the strongest, with an impressive track record of relevant experience and high-caliber expertise,” said Rachael Fleurence, PhD, PCORI’s CER Methods and Infrastructure Program Director. “We believe they will provide effective coordination to ensure the success of the new National Patient-Centered Clinical Research Network.”
The Harvard Pilgrim team includes experts in data standards, data security and privacy, medical ethics, patient-reported outcomes, project management, and research communications and dissemination. It has a history of managing and coordinating similar initiatives, including the U.S. Food and Drug Administration’s Mini Sentinel Program and the National Institutes of Health’s Health Care Systems Research Collaboratory.
The directors of the Coordinating Center will be Richard Platt, MD, MS, Professor and Chair of the Harvard Medical School Department of Population Medicine at the Harvard Pilgrim Health Care Institute in Boston, and Robert Califf, MD, Vice Chancellor for Clinical and Translational Research, Director of the Duke Translational Medicine Institute, and Professor of Medicine in the Division of Cardiology at the Duke University Medical Center in Durham, N.C.
Additional expertise is provided by staff from AcademyHealth, Brookings Institution, Center for Democracy and Technology, Center for Medical Technology Policy, Group Health Research Institute, and Johns Hopkins University. In addition, America’s Health Insurance Plans, the national trade representing the health insurance industry, will support stakeholder engagement and RAND Corporation will lead external evaluation efforts.
Details on the National Patient-Centered Clinical Research Network and the role of the Coordinating Center can be found at our website and in a blog post by PCORI Executive Director Joe Selby, MD, MPH.
The Patient-Centered Outcomes Research Institute (PCORI) is an independent, non-profit organization authorized by Congress in 2010. Its mission is to fund research that will provide patients, their caregivers and clinicians with the evidence-based information needed to make better-informed health care decisions. PCORI is committed to continuously seeking input from a broad range of stakeholders to guide its work. More information is available at www.pcori.org.
SOURCE Patient-Centered Outcomes Research Institute