We propose to create a Collaboratory Coordinating Center (Collaboratory CC) to work with the NIH to produce, document, and disseminate standards, and to create durable infrastructure that facilitates multicenter studies and reuse of data. The Collaboratory CC will be based at Duke University, with participation by the Harvard Pilgrim Health Care Institute at Harvard Medical School, the Group Health Research Institute, Johns Hopkins University and the Center for Medical Technology Policy. Our investigators have established multi-center research collaborations using electronic health records (EHRs), convened stakeholders to transform clinical trials, developed new regulatory approaches, and pioneered the use of patient-reported outcomes (PROs) in clinical research. This team has extensive experience in conducting both conventional and cluster randomized clinical trials, quasi-experimental studies, and observational studies across the spectrum of health systems, including integrated delivery systems and health plans, academic health and science systems, and private practices. The critical importance of this effort is reinforced by recent literature demonstrating that the vast majority of medical decisions are not supported by high quality evidence and that the clinical trials system is focused on small trials without sufficient power to fully inform practice or policy. In the face of this evidence gap the Institute of Medicine has called for a transformation of clinical trials rather than incremental improvements. This transformation should deal with the current fundamental separation of the conduct of clinical trials from the delivery of clinical care by involving practitioners and their health systems in th design and interpretation of trials, providing the broad education needed to enhance the value of practitioner participation and using the data collected as part of healthcare delivery as the core data source for the full spectrum of clinical research, from registries to observational studies an randomized trials. We believe that we are at a tipping point, that if propelled by a powerful Collaboratory effort, will enjoin multiple public and private entities towards the common goal of a Learning Health System. At the end of the five-year funding period, new policies, procedures, governance capabilities, and a substantial infrastructure will enable larger, simpler, less expensive and more relevant clinical trials that will be an integral component of the healthcare system.

Public Health Relevance

The NIH Health Systems Research Collaboratory proposes to transform the conduct of clinical trials in the US by conducting trials using electronic health records in the context of integrated health systems. This approach could dramatically reduce the cost and increase the efficiency of clinical trials. By increasing the rate of evidence generation and the generalizability of the research findings, the Collaboratory could result in significant reduction in death and disability.

Agency
National Institute of Health (NIH)
Institute
National Center for Complementary & Alternative Medicine (NCCAM)
Type
Specialized Center--Cooperative Agreements (U54)
Project #
4U54AT007748-05
Application #
9131616
Study Section
Special Emphasis Panel (ZAT1)
Program Officer
Weber, Wendy J
Project Start
2012-09-30
Project End
2017-08-31
Budget Start
2016-09-01
Budget End
2017-08-31
Support Year
5
Fiscal Year
2016
Total Cost
Indirect Cost
Name
Duke University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
044387793
City
Durham
State
NC
Country
United States
Zip Code
27705
Riley, Isaretta L; Boulware, L Ebony; Sun, Jie-Lena et al. (2018) Factors associated with reporting results for pulmonary clinical trials in ClinicalTrials.gov. Clin Trials 15:87-94
Li, Fan; Turner, Elizabeth L; Heagerty, Patrick J et al. (2017) An evaluation of constrained randomization for the design and analysis of group-randomized trials with binary outcomes. Stat Med 36:3791-3806
Zatzick, Douglas F; Rowhani-Rahbar, Ali; Wang, Jin et al. (2017) The Cumulative Burden of Mental, Substance Use, and General Medical Disorders and Rehospitalization and Mortality After an Injury. Psychiatr Serv 68:596-602
Locklear, Tracie; DeBar, Lynn L; Willig, James et al. (2017) Case Studies from the Clinic: Initiating and Implementing Patient-Reported Outcome Measures. EGEMS (Wash DC) 5:7
Simon, Gregory E; Coronado, Gloria; DeBar, Lynn L et al. (2017) Data Sharing and Embedded Research. Ann Intern Med 167:668-670
Weinfurt, Kevin P; Bollinger, Juli M; Brelsford, Kathleen M et al. (2017) Comparison of Approaches for Notification and Authorization in Pragmatic Clinical Research Evaluating Commonly Used Medical Practices. Med Care 55:970-978
Weinfurt, Kevin P; Hernandez, Adrian F; Coronado, Gloria D et al. (2017) Pragmatic clinical trials embedded in healthcare systems: generalizable lessons from the NIH Collaboratory. BMC Med Res Methodol 17:144
Anderson, Monique L; Nichol, Graham; Dai, David et al. (2016) Association Between Hospital Process Composite Performance and Patient Outcomes After In-Hospital Cardiac Arrest Care. JAMA Cardiol 1:37-45
Richesson, Rachel L; Smerek, Michelle M; Blake Cameron, C (2016) A Framework to Support the Sharing and Reuse of Computable Phenotype Definitions Across Health Care Delivery and Clinical Research Applications. EGEMS (Wash DC) 4:1232
Topazian, Rachel; Bollinger, Juli; Weinfurt, Kevin P et al. (2016) Physicians' perspectives regarding pragmatic clinical trials. J Comp Eff Res 5:499-506

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