Living with young-onset dementia in the family – a mixed method study

A-S. Helvika The Norwegian National Centre for Ageing and Health, Vestfold Hospital Trust, Tønsberg, Norway;b Department of Public Health and Nursing, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology (NTNU), Trondheim, NorwayView further author information

L. Hvidstenc Division for Mental Health and Addiction, Vestfold Hospital Trust, Tønsberg, NorwayView further author information

K. Engedala The Norwegian National Centre for Ageing and Health, Vestfold Hospital Trust, Tønsberg, NorwayView further author information

H. Kerstena The Norwegian National Centre for Ageing and Health, Vestfold Hospital Trust, Tønsberg, Norway;d Department of Research, Telemark Hospital Trust, Skien, Norway;e Department of Pharmacy, Section for Pharmacology and Pharmaceutical Biosciences, University of Oslo, Oslo, NorwayView further author information

M. C. N. Douradof Institute of Psychiatry, Universidade Federal do Rio de Janeiro – UFRJ, Rio de Janeiro, BrazilView further author information

A. Johannessena The Norwegian National Centre for Ageing and Health, Vestfold Hospital Trust, Tønsberg, Norway;g University of South-Eastern Norway - USN, Horten, NorwayCorrespondence[email protected]
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Living with young-onset dementia in the family – a mixed method study

Table 1. Characteristics of the carers and the persons with young-onset dementia (YOD) in the quantitative part of the study.

Table 2. Characteristics of the carers and the persons with young-onset dementia (YOD) in the qualitative part of the study.

Table 3. Overview of the questions asked to the carers of a person with young-onset dementia (YOD).

Table 4. Needs reported quantitatively by the carers, n = 74.

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Living with young-onset dementia in the family – a mixed method study

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Table 1. Characteristics of the carers and the persons with young-onset dementia (YOD) in the quantitative part of the study.

Table 2. Characteristics of the carers and the persons with young-onset dementia (YOD) in the qualitative part of the study.

Table 3. Overview of the questions asked to the carers of a person with young-onset dementia (YOD).

Table 4. Needs reported quantitatively by the carers, n = 74.

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