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Authors
Ambasta, Anshula https://orcid.org/0000-0003-0211-8654
Holroyd-Leduc, Jayna M.
Pokharel, Surakshya
Mathura, Pamela
Shih, Andrew Wei-Yeh
Stelfox, Henry T.
Ma, Irene
Harrison, Mark
Manns, Braden
Faris, Peter
Williamson, Tyler
Shukalek, Caley
Santana, Maria
Omodon, Onyebuchi
McCaughey, Deirdre
Kassam, Narmin
Naugler, Chris
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Funding
Funding for this research was provided by:
Canadian Institutes of Health Research (PJT- 183833)
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Article History
Received: 29 April 2024
Accepted: 23 June 2024
First Online: 2 July 2024
Declarations
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: This protocol has been approved by the University of British Columbia Clinical Research Ethics Board (H22-03005). Operational approval has also been obtained from all five participating health authorities in British Columbia. Since project activities are part of core operational process change, involve minimal risk to participants, and it is impracticable to obtain individual consent, we have obtained waiver of consent for healthcare provider and patient participants who will receive information about tools from the intervention bundle without any obligation to use them. We will obtain digital informed consent for healthcare provider participation in the online educational module and informed consent for participation in group audit and feedback discussions around laboratory test utilization data.
: Not applicable.
: The authors have no relevant conflicts of interest to disclose.
