Needs and quality of life of people with middle-stage dementia and their family carers from the European Actifcare study. When informal care alone may not suffice

Liselot Kerpershoek, Marjolein de Vugt, Claire Wolfs, Bob Woods, Hannah Jelley, Martin Orrell, Astrid Stephan, Anja Bieber, Gabriele Meyer, Geir Selbaek, Ron Handels, Anders Wimo, Louise Hopper, Kate Irving, Maria Marques, Manuel Gonçalves-Pereira, Elisa Portolani, Orazio Zanetti, Frans Verhey

Research output: Contribution to journalArticle

13 Citations (Scopus)

Abstract

OBJECTIVE: The Actifcare (Access to timely formal care) study investigated needs of people with dementia and their families during the phase in which formal care is being considered, and examined whether higher need levels are related to lower quality of life (QOL).

METHOD: From eight European countries 451 people with dementia and their carers participated. Needs were measured with the Camberwell Assessment of Need for the Elderly. QOL was measured with the QOL-AD, and carer quality of life was measured with the CarerQol. The relationship between needs and QOL was analysed with multiple regression analyses.

RESULTS: Needs were expressed in the domains of psychological distress, daytime activities, company and information. People with dementia rated their unmet needs significantly lower than their carers: the mean number of self-rated unmet needs was 0.95, whereas the mean proxy ratings were 1.66. For met needs, the self-rated mean was 5.5 and was 8 when proxy-rated. The level of needs reported was negatively associated with QOL for both.

CONCLUSION: The study results show that informal carers reported almost twice as many needs as people with dementia. The domains in which needs are expressed should be the primary focus for interventions to support QOL. The perspectives of people with dementia are informative when identifying needs.

Original languageEnglish
Article numberSI
Pages (from-to)897-902
Number of pages6
JournalAging & Mental Health
Volume22
Issue number7
Early online date25 Oct 2017
DOIs
Publication statusPublished - 2018

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Caregivers
Dementia
Patient Care
Quality of Life
Proxy
Needs Assessment
Regression Analysis
Psychology

Keywords

  • (un)met needs
  • Dementia
  • informal carer
  • quality of life

Cite this

Kerpershoek, Liselot ; de Vugt, Marjolein ; Wolfs, Claire ; Woods, Bob ; Jelley, Hannah ; Orrell, Martin ; Stephan, Astrid ; Bieber, Anja ; Meyer, Gabriele ; Selbaek, Geir ; Handels, Ron ; Wimo, Anders ; Hopper, Louise ; Irving, Kate ; Marques, Maria ; Gonçalves-Pereira, Manuel ; Portolani, Elisa ; Zanetti, Orazio ; Verhey, Frans. / Needs and quality of life of people with middle-stage dementia and their family carers from the European Actifcare study. When informal care alone may not suffice. In: Aging & Mental Health. 2018 ; Vol. 22, No. 7. pp. 897-902.
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abstract = "OBJECTIVE: The Actifcare (Access to timely formal care) study investigated needs of people with dementia and their families during the phase in which formal care is being considered, and examined whether higher need levels are related to lower quality of life (QOL).METHOD: From eight European countries 451 people with dementia and their carers participated. Needs were measured with the Camberwell Assessment of Need for the Elderly. QOL was measured with the QOL-AD, and carer quality of life was measured with the CarerQol. The relationship between needs and QOL was analysed with multiple regression analyses.RESULTS: Needs were expressed in the domains of psychological distress, daytime activities, company and information. People with dementia rated their unmet needs significantly lower than their carers: the mean number of self-rated unmet needs was 0.95, whereas the mean proxy ratings were 1.66. For met needs, the self-rated mean was 5.5 and was 8 when proxy-rated. The level of needs reported was negatively associated with QOL for both.CONCLUSION: The study results show that informal carers reported almost twice as many needs as people with dementia. The domains in which needs are expressed should be the primary focus for interventions to support QOL. The perspectives of people with dementia are informative when identifying needs.",
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Kerpershoek, L, de Vugt, M, Wolfs, C, Woods, B, Jelley, H, Orrell, M, Stephan, A, Bieber, A, Meyer, G, Selbaek, G, Handels, R, Wimo, A, Hopper, L, Irving, K, Marques, M, Gonçalves-Pereira, M, Portolani, E, Zanetti, O & Verhey, F 2018, 'Needs and quality of life of people with middle-stage dementia and their family carers from the European Actifcare study. When informal care alone may not suffice', Aging & Mental Health, vol. 22, no. 7, SI, pp. 897-902. https://doi.org/10.1080/13607863.2017.1390732

Needs and quality of life of people with middle-stage dementia and their family carers from the European Actifcare study. When informal care alone may not suffice. / Kerpershoek, Liselot; de Vugt, Marjolein; Wolfs, Claire; Woods, Bob; Jelley, Hannah; Orrell, Martin; Stephan, Astrid; Bieber, Anja; Meyer, Gabriele; Selbaek, Geir; Handels, Ron; Wimo, Anders; Hopper, Louise; Irving, Kate; Marques, Maria; Gonçalves-Pereira, Manuel; Portolani, Elisa; Zanetti, Orazio; Verhey, Frans.

In: Aging & Mental Health, Vol. 22, No. 7, SI, 2018, p. 897-902.

Research output: Contribution to journalArticle

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T1 - Needs and quality of life of people with middle-stage dementia and their family carers from the European Actifcare study. When informal care alone may not suffice

AU - Kerpershoek, Liselot

AU - de Vugt, Marjolein

AU - Wolfs, Claire

AU - Woods, Bob

AU - Jelley, Hannah

AU - Orrell, Martin

AU - Stephan, Astrid

AU - Bieber, Anja

AU - Meyer, Gabriele

AU - Selbaek, Geir

AU - Handels, Ron

AU - Wimo, Anders

AU - Hopper, Louise

AU - Irving, Kate

AU - Marques, Maria

AU - Gonçalves-Pereira, Manuel

AU - Portolani, Elisa

AU - Zanetti, Orazio

AU - Verhey, Frans

PY - 2018

Y1 - 2018

N2 - OBJECTIVE: The Actifcare (Access to timely formal care) study investigated needs of people with dementia and their families during the phase in which formal care is being considered, and examined whether higher need levels are related to lower quality of life (QOL).METHOD: From eight European countries 451 people with dementia and their carers participated. Needs were measured with the Camberwell Assessment of Need for the Elderly. QOL was measured with the QOL-AD, and carer quality of life was measured with the CarerQol. The relationship between needs and QOL was analysed with multiple regression analyses.RESULTS: Needs were expressed in the domains of psychological distress, daytime activities, company and information. People with dementia rated their unmet needs significantly lower than their carers: the mean number of self-rated unmet needs was 0.95, whereas the mean proxy ratings were 1.66. For met needs, the self-rated mean was 5.5 and was 8 when proxy-rated. The level of needs reported was negatively associated with QOL for both.CONCLUSION: The study results show that informal carers reported almost twice as many needs as people with dementia. The domains in which needs are expressed should be the primary focus for interventions to support QOL. The perspectives of people with dementia are informative when identifying needs.

AB - OBJECTIVE: The Actifcare (Access to timely formal care) study investigated needs of people with dementia and their families during the phase in which formal care is being considered, and examined whether higher need levels are related to lower quality of life (QOL).METHOD: From eight European countries 451 people with dementia and their carers participated. Needs were measured with the Camberwell Assessment of Need for the Elderly. QOL was measured with the QOL-AD, and carer quality of life was measured with the CarerQol. The relationship between needs and QOL was analysed with multiple regression analyses.RESULTS: Needs were expressed in the domains of psychological distress, daytime activities, company and information. People with dementia rated their unmet needs significantly lower than their carers: the mean number of self-rated unmet needs was 0.95, whereas the mean proxy ratings were 1.66. For met needs, the self-rated mean was 5.5 and was 8 when proxy-rated. The level of needs reported was negatively associated with QOL for both.CONCLUSION: The study results show that informal carers reported almost twice as many needs as people with dementia. The domains in which needs are expressed should be the primary focus for interventions to support QOL. The perspectives of people with dementia are informative when identifying needs.

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