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Advance Consent in Acute Stroke Trials: Survey of Canadian Stroke Physicians

  • Ubong Udoh
  • , Brian Dewar
  • , Stuart Nicholls
  • , Mark Fedyk
  • , Robert Fahed
  • , Jeff Perry
  • , Michael D. Hill
  • , Bijoy Menon
  • , Richard H. Swartz
  • , Alexandre Y. Poppe
  • , Sophia Gocan
  • , Jamie Brehaut
  • , Katie Dainty
  • , Victoria Shepherd
  • , Dar Dowlatshahi
  • , Michel Shamy*
  • *Corresponding author for this work
  • University of Ottawa
  • University of California at Davis
  • University of Calgary
  • University of Toronto
  • Centre Hospitalier de L'Universite de Montreal
  • North York General Hospital
  • Cardiff University

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

Advance consent presents a potential solution to the challenge of obtaining informed consent for participation in acute stroke trials. Clinicians in stroke prevention clinics are uniquely positioned to identify and seek consent from potential stroke trial participants. To assess the acceptability of advance consent to Canadian stroke clinic physicians, we performed an online survey. We obtained 58 respondents (response rate 35%): the vast majority (82%) expressed comfort with obtaining advance consent and 92% felt that doing so would not be a significant disruption to clinic workflow. These results support further study of advance consent for acute stroke trials.

Original languageEnglish
Pages (from-to)122-125
Number of pages4
JournalCanadian Journal of Neurological Sciences
Volume51
Issue number1
DOIs
StatePublished - 17 Jan 2024
Externally publishedYes

Keywords

  • Advance directives
  • Consent
  • Research ethics

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