Advocating the rights of people with dementia to contribute to research: Considerations for researchers and ethics committees

被引:13
|
作者
O'Connor, Claire M. C. [1 ,2 ]
Liddle, Jacki [3 ]
O'Reilly, Maria [4 ]
Meyer, Claudia [5 ,6 ]
Cartwright, Jade [7 ]
Chisholm, Marita [8 ]
Conway, Erin [9 ]
Fielding, Elaine [10 ]
Fox, Amanda [10 ]
MacAndrew, Margaret [10 ]
Schnitker, Linda [11 ]
Travers, Catherine [3 ,10 ]
Watson, Karen [12 ]
While, Christine [13 ]
Bail, Kasia [14 ]
机构
[1] HammondCare, Ctr Posit Ageing, Sydney, NSW, Australia
[2] Univ New South Wales, Sch Populat Hlth, Sydney, NSW, Australia
[3] Univ Queensland, Brisbane, Qld, Australia
[4] Cent Queensland Univ, Bundaberg, Qld, Australia
[5] Bolton Clarke Res Inst, Melbourne, Vic, Australia
[6] Monash Univ, Rehabil Ageing & Independent Living Res Ctr, Melbourne, Vic, Australia
[7] Curtin Univ, Perth, WA, Australia
[8] Rural North West Hlth, Warracknabeal, Vic, Australia
[9] Australian Catholic Univ, Fac Hlth Sci, Brisbane, Qld, Australia
[10] Queensland Univ Technol, Brisbane, Qld, Australia
[11] Bolton Clarke Res Inst, Brisbane, Qld, Australia
[12] Univ Sydney, Sydney, NSW, Australia
[13] La Trobe Univ, Dementia Training Australia, Melbourne, Vic, Australia
[14] Univ Canberra, Fac Hlth, Canberra, ACT, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
dementia; ethics committees; informed consent; research; social participation; INFORMED-CONSENT;
D O I
10.1111/ajag.13023
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Objective Research involving people with dementia is vital to appropriately inform policy and practice decisions affecting this population. As dementia-care researchers, we frequently advocate to Human Research Ethics Committees for the right of people with dementia to choose whether to participate in research. This brief report provides some considerations for researchers and ethics committees. Method Descriptive summary of principles that argue for inclusion of people with dementia in research studies. Results Specifically excluding people living with dementia from research because of perceived cognitive impairment is inappropriate in light of human rights principles and the right to contribute to evidence-based care. Conclusion There is a difference between capacity to provide informed consent and ability to provide perspectives that are valid for each individual. Providing the opportunity for a person with dementia to participate in research and offering support to do this is a matter of human rights.
引用
收藏
页码:309 / 313
页数:5
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