Order:
Disambiguations
Robert Boruch [4]R. Boruch [1]Robert F. Boruch [1]
  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.
    Translate
     
     
    Export citation  
     
    Bookmark   13 citations  
  2. Ethical Issues Posed by Cluster Randomized Trials in Health Research.Charles Weijer, Jeremy M. Grimshaw, Monica Taljaard, Ariella Binik, Robert Boruch, Jamie C. Brehaut, Allan Donner, Martin P. Eccles, Antonio Gallo, Andrew D. McRae & Ray Saginur - 2011 - Trials 1 (12):100.
    No categories
     
    Export citation  
     
    Bookmark   9 citations  
  3. 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.
    No categories
     
    Export citation  
     
    Bookmark   8 citations  
  4.  8
    Composition of Episodic Memory.Benton J. Underwood, Robert F. Boruch & Robert A. Malmi - 1978 - Journal of Experimental Psychology: General 107 (4):393-419.
  5. 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.
    No categories
     
    Export citation  
     
    Bookmark   3 citations  
  6.  25
    Reporting of Patient Consent in Healthcare Cluster Randomised Trials is Associated with the Type of Study Interventions and Publication Characteristics.A. McRae, M. Taljaard, C. Weijer, C. Bennett, Z. Skea, R. Boruch, J. Brehaut, M. Eccles, J. Grimshaw & A. Donner - 2013 - Journal of Medical Ethics 39 (2):119-124.
    Objective Cluster randomised trial (CRT) investigators face challenges in seeking informed consent from individual patients (cluster members). This study examined associations between reporting of patient consent in healthcare CRTs and characteristics of these trials. Study design Consent practices and study characteristics were abstracted from a random sample of 160 CRTs performed in primary or hospital care settings that were published from 2000 to 2008. Multivariable logistic regression was used to examine associations between reporting of patient consent and methodological characteristics, as (...)
    Direct download (5 more)  
     
    Export citation  
     
    Bookmark