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Reporting of patient consent in healthcare cluster randomised trials is associated with the type of study interventions and publication characteristics
  1. Andrew McRae1,
  2. Monica Taljaard2,
  3. Charles Weijer3,
  4. Carol Bennett2,
  5. Zoe Skea4,
  6. Robert Boruch5,
  7. Jamie Brehaut2,
  8. Martin Eccles6,
  9. Jeremy Grimshaw2,
  10. Allan Donner7
  1. 1Department of Emergency Medicine, University of Calgary, Calgary, Alberta, Canada
  2. 2Ottawa Hospital Research Institute, Ottawa, Ontario, Canada
  3. 3Rotman Institute of Philosophy, Department of Philosophy, Western University, London, Ontario, Canada
  4. 4University of Aberdeen, Aberdeen, UK
  5. 5University of Pennsylvania, Philadelphia, Pennsylvania, USA
  6. 6University of Newcastle, Newcastle, UK
  7. 7Department of Epidemiology and Biostatistics, University of Western Ontario, London, Ontario, Canada
  1. Correspondence to Dr Andrew McRae, Department of Emergency Medicine, University of Calgary, Unit 1633, 1632 14th Ave NW, Calgary, Alberta T2N 1M7, Canada;Andrew.McRae{at}albertahealthservices.ca

Abstract

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 well as publication features such as date and journal of publication.

Results 82 (53.8%) of 160 studies reported obtaining informed consent from individual patients. Reporting of patient consent was independently and positively associated with: smaller cluster size, the evaluation of experimental interventions targeted at patients, data collection from individual patients, publication later than 2004 and publication in higher-impact journals.

Conclusions Reporting of consent practices in published CRTs should be improved. Consent practices in published CRTs appear to be related to the type of interventions under study, as well as journal impact and trends in research ethics practices. These findings will inform best practices in trial conduct and ethics review, remediation of errors in consent practices and ethics review and the development of regulatory guidance for CRTs.

  • Informed Consent
  • Research Ethics
  • Scientific Research
  • Statistics
  • Public Health Ethics

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