Alzheimer’s disease; perceived rights; social distance; stigmatization; health professionals; laypeople
Résumé :
[en] The present study investigated how laypeople and professionals (N = 185) judge the rights of a person affected with Alzheimer’s disease (AD) and whether social distance exists towards this person. Participants completed a questionnaire after reading a vignette describing a target person with an early stage of AD. Half of the participants responded to a female target, the other half responded to a male target. Results showed that rights and competencies of the persons are rated high and social distance is exhibited only to a lesser degree, although there was a significant difference between the male and female target. Furthermore, health professionals approved more rights than laypeople, which suggests that there is a need for more detailed information about this disease in the general population.
Disciplines :
Sciences sociales & comportementales, psychologie: Multidisciplinaire, généralités & autres
Auteur, co-auteur :
BOURKEL, Elisabeth ; University of Luxembourg > Faculty of Language and Literature, Humanities, Arts and Education (FLSHASE) > Integrative Research Unit: Social and Individual Development (INSIDE)
FERRING, Dieter ; University of Luxembourg > Faculty of Language and Literature, Humanities, Arts and Education (FLSHASE) > Integrative Research Unit: Social and Individual Development (INSIDE)
Weber, Germain; Universität Wien > Fakultät für Psychologie > Institut für angewandte Psychologie: Gesundheit, Entwicklung und Förderunng
Langue du document :
Anglais
Titre :
Perceived rights of and social distance to people with Alzheimer's disease
Date de publication/diffusion :
2012
Titre du périodique :
GeroPsych: Journal of Gerontopsychology and Geriatric Psychiatry