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Participation of persons living with dementia in research : A means to address epistemic injustice

Publiceringsår

2024

Upphovspersoner

Halonen, Ulla; Aaltonen, Mari ; Van Aerschot, Lina; Pirhonen, Jari Pentti Tapio

Abstrakt

Epistemic injustice refers to wronging or mistreating individuals in terms of their capacity as knowers, based on prejudices or negative attitudes. Excluding people with dementia from research is a form of epistemic injustice. In this article, we discuss epistemic injustice associated with data collection processes and the participation of people with dementia in scientific research. The challenges of participation that we discuss pertain to the role of gatekeepers and ethical research perspectives. The arguments presented are based on previous research, experiences from our current project, and critical self-assessment regarding the latter. The aim is to shed light on what enables or prevents people living with dementia from participating in research, and how this is connected to epistemic injustice. It is known that prejudices related to dementia affect both researchers and people living with dementia: the former tend to exclude people with dementia, and the latter may practice self-silencing due to dementia-related stigma. In addition to these individual issues, we argue that epistemic injustice occurs at a structural level, where a major role is played by gatekeepers and research ethics panels. As close family members, health officials, and dementia-related associations are the main gatekeepers, their attitudes and perceptions are highlighted. In terms of ethical issues, the concept of informed consent needs to be elaborated. If the research is not expected to harm participants and may contribute to improving the lives of those with dementia, the perspective should be shifted from informed consent to ongoing consent assessment. While acknowledging the features and symptoms of dementia, researchers should be more courageous, trust in the good cause, and enable persons living with dementia to participate in research that concerns them. This is the only way for researchers to genuinely understand the social world, experiences, and needs of those with dementia and to address epistemic injustice.
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Organisationer och upphovspersoner

Helsingfors universitet

Pirhonen Jari Pentti Tapio

Tammerfors universitet

Pirhonen Jari Orcid -palvelun logo

Van Aerschot Lina Orcid -palvelun logo

Jyväskylä universitet

Van Aerschot Lina Orcid -palvelun logo

Halonen Ulla Orcid -palvelun logo

Publikationstyp

Publikationsform

Artikel

Moderpublikationens typ

Tidning

Artikelstyp

En originalartikel

Målgrupp

Vetenskaplig

Kollegialt utvärderad

Kollegialt utvärderad

UKM:s publikationstyp

A1 Originalartikel i en vetenskaplig tidskrift

Publikationskanalens uppgifter

Journal

Dementia

Moderpublikationens namn

Dementia

Publikationsforum

54562

Publikationsforumsnivå

1

Öppen tillgång

Öppen tillgänglighet i förläggarens tjänst

Ja

Öppen tillgång till publikationskanalen

Delvis öppen publikationskanal

Licens för förläggarens version

CC BY

Parallellsparad

Ja

Övriga uppgifter

Vetenskapsområden

Hälsovetenskap; Sociologi; Social- och samhällspolitik

Nyckelord

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Publiceringsland

Förenade kungariket

Förlagets internationalitet

Internationell

Språk

engelska

Internationell sampublikation

Nej

Sampublikation med ett företag

Nej

DOI

10.1177/14713012241299015

Publikationen ingår i undervisnings- och kulturministeriets datainsamling

Ja