Background Upon the WHO declaration of COVID-19 as a pandemic, healthcare workers (HCWs) - unvaccinated by necessity - were celebrated as “heroes” for their service under difficult conditions. Later, as some of them resisted vaccine mandates, they were reframed as “threats”, regardless of personal behaviour, workplace setting, or evidence of their harmfulness. This discursive shift and the institutional mechanisms supporting it remain underexamined.
Goal This protocol outlines a mixed-method study investigating the implementation of COVID-19 vaccine mandates in medical establishments across Ontario, Canada.
Methods This is a two-phase mixed methods planned study. Phase 1 is an environmental scan of institutional vaccine mandate policies across a purposive sample of diverse Ontario medical establishments. It will track policy implementation timelines, mandates scope, exemptions eligibility criteria, and supporting scientific evidence presented. Phase 2 is a critical interpretive analysis of documents collected in Phase 1 that draws on Max Weber’s theory of bureaucracy and legitimacy, Carol Bacchi’s “What Is the Problem Represented to Be” (WPR) approach, and Brian Martin’s framework on suppression of dissent to identify patters in the institutional framing and treatment of challenges to mandated vaccination.
Expected Outcomes This study is expected to yield descriptive and interpretive insights into how bureaucratic structures shaped mandate enforcement and dissent suppression. Results are expected to inform academic debates on institutional legitimacy, governance, and public health ethics.
Competing Interest StatementThe authors have declared no competing interest.
Funding StatementThis study did not receive any funding
Author DeclarationsI confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.
Yes
I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.
Yes
I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).
Yes
I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.
Yes
Data AvailabilityAll data in the present protocol are contained in the manuscript
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