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  1. Does Clinical Equipoise Apply to Cluster Randomized Trials in Health Research?Ariella Binik, Charles Weijer, Andrew McRae, Jeremy Grimshaw, Monica Taljaard, Robert Boruch, Jamie Brehaut, Allan Donner, Martin Eccles, Antonio Gallo, Raphael Saginur & Merrick Zwarenstein - 2011 - Trials 12.
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  2. When is Informed Consent Required in Cluster Randomized Trials in Health Research?Andrew D. McRae, Ariella Binik, Charles Weijer, Angela White, Jeremy M. Grimshaw, Robert Boruch, Jamie C. Brehaut, Allan Donner, Martin P. Eccles, Raphael Saginur, Merrick Zwarenstein & Monica Taljaard - 2011 - Trials 1 (12):202.
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  3. Who is the Research Subject in Cluster Randomized Trials in Health Research?Andrew D. McRae, Ariella Binik, Charles Weijer, Jeremy M. Grimshaw, Monica Taljaard, Robert Boruch, Jamie C. Brehaut, Allan Donner, Martin P. Eccles, Antonio Gallo, Ray Saginur & Merrick Zwarenstein - 2011 - Trials 1 (12):118.
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  4.  15
    The Doctor–Nurse Game in the Age of Interprofessional Care: A View From Canada.Scott Reeves, Sioban Nelson & Merrick Zwarenstein - 2008 - Nursing Inquiry 15 (1):1-2.
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  5.  24
    Stakeholder Views Regarding Ethical Issues in the Design and Conduct of Pragmatic Trials: Study Protocol.Stuart G. Nicholls, Kelly Carroll, Jamie Brehaut, Charles Weijer, Spencer Phillips Hey, Cory E. Goldstein, Merrick Zwarenstein, Ian D. Graham, Joanne E. McKenzie, Lauralyn McIntyre, Vipul Jairath, Marion K. Campbell, Jeremy M. Grimshaw, Dean A. Fergusson & Monica Taljaard - 2018 - BMC Medical Ethics 19 (1):90.
    Randomized controlled trial trial designs exist on an explanatory-pragmatic spectrum, depending on the degree to which a study aims to address a question of efficacy or effectiveness. As conceptualized by Schwartz and Lellouch in 1967, an explanatory approach to trial design emphasizes hypothesis testing about the mechanisms of action of treatments under ideal conditions, whereas a pragmatic approach emphasizes testing effectiveness of two or more available treatments in real-world conditions. Interest in, and the number of, pragmatic trials has grown substantially (...)
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    The Importance of Describing as Well as Defining Usual Care.Stuart G. Nicholls, Merrick Zwarenstein & Monica Taljaard - 2020 - American Journal of Bioethics 20 (1):56-58.
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    Electronic Prescribing in an Ambulatory Care Setting: A Cluster Randomized Trial.Katie N. Dainty, Neill K. J. Adhikari, Alex Kiss, Sherman Quan & Merrick Zwarenstein - 2012 - Journal of Evaluation in Clinical Practice 18 (4):761-767.
  8.  10
    Consensus on Interprofessional Collaboration in Hospitals: Statistical Agreement of Ratings From Ethnographic Fieldwork and Measurement Scales.Chris Kenaszchuk, Lesley Gotlib Conn, Katie Dainty, Colleen McCarthy, Scott Reeves & Merrick Zwarenstein - 2012 - Journal of Evaluation in Clinical Practice 18 (1):93-99.
  9. Protocol for the Development of a CONSORT Extension for RCTs Using Cohorts and Routinely Collected Health Data.Brett D. Thombs, David Torgerson, Maureen Sauvé, David Erlinge, Eric I. Benchimol, Helena M. Verkooijen, Rudolf Uher, Lehana Thabane, Tjeerd P. van Staa, Kimberly A. Mc Cord, Marion K. Campbell, Philippe Ravaud, Isabelle Boutron, David Moher, Sinéad M. Langan, Merrick Zwarenstein, Chris Gale, Clare Relton, Ole Fröbert, Margaret Sampson, Lars G. Hemkens, Edmund Juszczak & Linda Kwakkenbos - 2018 - Research Integrity and Peer Review 3 (1).
    BackgroundRandomized controlled trials are often complex and expensive to perform. Less than one third achieve planned recruitment targets, follow-up can be labor-intensive, and many have limited real-world generalizability. Designs for RCTs conducted using cohorts and routinely collected health data, including registries, electronic health records, and administrative databases, have been proposed to address these challenges and are being rapidly adopted. These designs, however, are relatively recent innovations, and published RCT reports often do not describe important aspects of their methodology in a (...)
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