Outcomes valued by people living with dementia and their care partners: protocol for a qualitative systematic review and synthesis

被引:0
|
作者
Booi, Laura [1 ]
Wheatley, Alison [1 ]
Brunskill, Greta [1 ]
Banerjee, Sube [2 ]
Manthorpe, Jill [3 ]
Robinson, Louise [1 ]
Bamford, Claire [1 ]
机构
[1] Newcastle Univ, Fac Med Sci, Populat Hlth Sci Inst, Newcastle Upon Tyne, Tyne & Wear, England
[2] Univ Plymouth, Off Vice Chancellor, Plymouth, Devon, England
[3] Kings Coll London, Policy Inst Kings, NIHR Policy Res Unit Hlth & Social Care, London, England
来源
BMJ OPEN | 2021年 / 11卷 / 08期
关键词
dementia; qualitative research; primary care; OPTIMAL SEARCH STRATEGIES; RELEVANT; TRIALS; HEALTH; NEEDS; SET;
D O I
10.1136/bmjopen-2021-050909
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction Growing numbers of interventions are being developed to support people and families living with dementia, but the extent to which they address the areas of most importance to the intended recipients is unclear. This qualitative review will synthesise outcomes identified as important from the perspectives of people living with dementia and their care partners, both for themselves and each other. Methods and analysis The review will employ thematic synthesis methodology. Studies from 1990 or later will be eligible if they include qualitative data on the views of people living with dementia or their care partners on valued outcomes or the lived experience of dementia. Databases to be searched include MEDLINE, Cumulative Index to Nursing and Allied Health Literature (CINAHL), PsycInfo and Social Sciences Premium Collection, in addition to systematically gathered grey literature. Rayyan QCRI software will be used to manage the screening processes, and NVivo software will be used to manage data extraction and analysis. The review will also critically evaluate the extent to which international recommendations address the areas of importance to people living with dementia and their families. The findings will be of relevance to researchers, policy makers and providers and commissioners of dementia services. The protocol is written in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses Protocols guidelines. Ethics and dissemination As the methodology of this study consists of collecting data from publicly available articles, it does not require ethical approval. We will share the results through conference presentations and an open-access publication in a peer-reviewed journal. Our mixed stakeholder involvement group will advise on dissemination to non-academic audiences. PROSPERO registration number CRD42020219274.
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页数:7
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