Ethical and regulatory issues of pragmatic cluster randomized trials in contemporary health systems

Can RESEARCH and CARE Be Ethically Integrated?

(2015) EMILY A. LARGENT et al.   HASTINGS CENTER REPORT

Cluster Randomized Trials:Another Look

(2014) Ruth Macklin   HASTINGS CENTER REPORT

Ethics and Regulatory Complexities for Pragmatic Clinical Trials

(2014) Jeremy Sugarman et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

OHRP and Standard-of-Care Research

(2014)   NEW ENGLAND JOURNAL OF MEDICINE

How Variability in the Institutional Review Board Review Process Affects Minimal-Risk Multisite Health Services Research

(2013) Laura A. Petersen et al.   ANNALS OF INTERNAL MEDICINE

Informed Consent and Cluster-Randomized Trials

(2012) Julius Sim et al.   AMERICAN JOURNAL OF PUBLIC HEALTH

The Patient-Centered Outcomes Research Institute (PCORI) National Priorities for Research and Initial Research Agenda

(2012) Anne C. Beal   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

New NIH effort seeks to find ways to make trials run smoother

(2012) Susan Matthews   NATURE MEDICINE

Participant Informed Consent in Cluster Randomized Trials: Review

(2012) Bruno Giraudeau et al.   PLoS One

What is the role and authority of gatekeepers in cluster randomized trials in health research?

(2012) Antonio Gallo et al.   Trials

The Ottawa Statement on the Ethical Design and Conduct of Cluster Randomized Trials

(2012) Charles Weijer et al.   PLOS MEDICINE

How Best to Define the Concept of Minimal Risk

(2011) Anna E. Westra et al.   JOURNAL OF PEDIATRICS

Who is the research subject in cluster randomized trials in health research?

(2011) Andrew D McRae et al.   Trials

When is informed consent required in cluster randomized trials in health research?

(2011) Andrew D McRae et al.   Trials