Reconsidering frameworks of Alzheimer's dementia when assessing psychosocial outcomes

Alzheimer's and Dementia: Translational Research and Clinical Interventions - Tập 5 - Trang 388-397 - 2019
Joseph E. Gaugler1, Lisa J. Bain2, Lauren Mitchell3, Jessica Finlay4, Sam Fazio5, Eric Jutkowitz6
1Division of Health Policy and Management, School of Public Health, The University of Minnesota, Minneapolis, MN, USA
2The Alzheimer's Association, Chicago, IL, USA
3Minneapolis VA Healthcare System, Minneapolis, MN, USA
4Institute for Social Research, University of Michigan Ann Arbor, MI USA
5Care and Support, Alzheimer's Association, Chicago, IL, USA
6Department of Health Services, Policy & Practice, School of Public Health, Brown University, Providence, RI, USA

Tóm tắt

AbstractThe purpose of this introductory article to the special issue on psychosocial outcome measures in Alzheimer's & Dementia: Translational Research & Clinical Interventions is to outline new frameworks to more effectively capture and measure the full range of how people living with Alzheimer's dementia and their family caregivers experience the disease process. Specifically, we consider the strengths and weaknesses of alternative perspectives, including person‐centered, strength‐based, and resilience‐focused approaches that may complement and extend the dominant deficit paradigm to reflect the entirety of the dementia experience. Our aim is to encourage innovative methods to measure psychosocial aspects of Alzheimer's dementia and caregiving that have not yet received sufficient attention, including resources (e.g., services and supports) and positive caregiver and care recipient outcomes (e.g., positive mood and adaptation).

Tài liệu tham khảo

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Alzheimer's and Dementia: Translational Research and Clinical Interventions

Tập 5

388-397

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