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JBI systematic review protocol of text/opinions on how to best collect race-based data in healthcare contexts.
Quan, Cindy; Clark, Nancy; Costigan, Catherine L; Murphy, Jill; Li, Michael; David, Anita; Ganesan, Soma; Guzder, Jaswant; Cross, Barbara.
  • Quan C; Psychology, University of Victoria, Victoria, British Columbia, Canada cindyquan@uvic.ca.
  • Clark N; School of Nursing, University of Victoria, Victoria, British Columbia, Canada.
  • Costigan CL; Psychology, University of Victoria, Victoria, British Columbia, Canada.
  • Murphy J; Psychiatry, University of British Columbia, Vancouver, British Columbia, Canada.
  • Li M; Vancouver General Hospital, Vancouver, British Columbia, Canada.
  • David A; Lived Experience Strategic Advisor, BC Mental Health and Substance Use Services, Vancouver, British Columbia, Canada.
  • Ganesan S; Psychiatry, University of British Columbia, Vancouver, British Columbia, Canada.
  • Guzder J; Division of Social and Cultural Psychiatry, McGill University, Montreal, Québec, Canada.
  • Cross B; Vancouver General Hospital, Vancouver, British Columbia, Canada.
BMJ Open ; 13(5): e069753, 2023 05 16.
Article in English | MEDLINE | ID: covidwho-20241603
ABSTRACT

INTRODUCTION:

Racialized population groups have worse health outcomes across the world compared with non-racialized populations. Evidence suggests that collecting race-based data should be done to mitigate racism as a barrier to health equity, and to amplify community voices, promote transparency, accountability, and shared governance of data. However, limited evidence exists on the best ways to collect race-based data in healthcare contexts. This systematic review aims to synthesize opinions and texts on the best practices for collecting race-based data in healthcare contexts. METHODS AND ANALYSES We will use the Joanna Briggs Institute (JBI) method for synthesizing text and opinions. JBI is a global leader in evidence-based healthcare and provides guidelines for systematic reviews. The search strategy will locate both published and unpublished papers in English in CINAHL, Medline, PsycINFO, Scopus and Web of Science from 1 January 2013 to 1 January 2023, as well as unpublished studies and grey literature of relevant government and research websites using Google and ProQuest Dissertations and Theses. The Preferred Reporting Items for Systematic Reviews and Meta-Analyses statement methodology for systematic reviews of text and opinion will be applied, including screening and appraisal of the evidence by two independent reviewers and data extraction using JBI's Narrative, Opinion, Text, Assessment, Review Instrument. This JBI systematic review of opinion and text will address gaps in knowledge about the best ways to collect race-based data in healthcare. Improvements in race-based data collection, may be related to structural policies that address racism in healthcare. Community participation may also be used to increase knowledge about collecting race-based data. ETHICS AND DISSEMINATION The systematic review does not involve human subjects. Findings will be disseminated through a peer-reviewed publication in JBI evidence synthesis, conferences and media. PROSPERO REGISTRATION NUMBER CRD42022368270.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Delivery of Health Care / Health Facilities Type of study: Experimental Studies / Prognostic study / Qualitative research / Randomized controlled trials / Reviews / Systematic review/Meta Analysis Limits: Humans Language: English Journal: BMJ Open Year: 2023 Document Type: Article Affiliation country: Bmjopen-2022-069753

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Delivery of Health Care / Health Facilities Type of study: Experimental Studies / Prognostic study / Qualitative research / Randomized controlled trials / Reviews / Systematic review/Meta Analysis Limits: Humans Language: English Journal: BMJ Open Year: 2023 Document Type: Article Affiliation country: Bmjopen-2022-069753