TY - JOUR
T1 - Een ‘mixed-methods’ evaluatie-onderzoek naar voorkeuren van naasten en zorgprofessionals voor een handreiking over levenseindezorg bij dementie
AU - Bavelaar, Laura
AU - Visser, Mandy
AU - Dijkstra, Eva J.
AU - van der Steen, Jenny T.
AU - Sizoo, Eefje M.
N1 - Funding Information:
LUMC: Dit werk is uitgevoerd als onderdeel van een EU Joint Programme – Neurodegenerative Disease Research (JPND) project. Het project wordt in Nederland ondersteund door het ZonMw-programma Memorabel, met subsidienummer 733051084, onder het label van JPND – www.jpnd.eu.
Publisher Copyright:
© 2023, Vilans. All rights reserved.
PY - 2023
Y1 - 2023
N2 - A booklet was developed in Canada in 2005 to inform family caregivers of people with dementia about end-of-life care. A Dutch version was published in 2011 after evaluation and revision. Developments in research and society call for a second revision. The aim of this study was to map out users’ (family caregivers and healthcare professionals) preferences regarding the look and feel, and content of the booklet. To this end, in addition to the current paper booklet, we created a prototype website and app, along with three illustration options. Twenty-one family caregivers and nineteen healthcare professionals completed a questionnaire about their preferences. Open ended questions were analyzed using content analysis, multiple-choice questions using descriptive analysis. The participants valued the question-answer format. They perceived the text as too medically oriented and they expressed a need for more inclusive language and broader information. The participants found images of people suitable for the booklet and they preferred the illustrations to be less focused on the medical context. The participants preferred the paper booklet and a website. By understanding family caregivers’ and healthcare professionals’ preferences, in the second revision, the booklet can be tailored to the user. It is expected that this tailoring will support informing family caregivers about end-of-life care.
AB - A booklet was developed in Canada in 2005 to inform family caregivers of people with dementia about end-of-life care. A Dutch version was published in 2011 after evaluation and revision. Developments in research and society call for a second revision. The aim of this study was to map out users’ (family caregivers and healthcare professionals) preferences regarding the look and feel, and content of the booklet. To this end, in addition to the current paper booklet, we created a prototype website and app, along with three illustration options. Twenty-one family caregivers and nineteen healthcare professionals completed a questionnaire about their preferences. Open ended questions were analyzed using content analysis, multiple-choice questions using descriptive analysis. The participants valued the question-answer format. They perceived the text as too medically oriented and they expressed a need for more inclusive language and broader information. The participants found images of people suitable for the booklet and they preferred the illustrations to be less focused on the medical context. The participants preferred the paper booklet and a website. By understanding family caregivers’ and healthcare professionals’ preferences, in the second revision, the booklet can be tailored to the user. It is expected that this tailoring will support informing family caregivers about end-of-life care.
KW - Booklet
KW - Dementia
KW - Family caregiver
KW - Palliative care
UR - https://www.scopus.com/pages/publications/85163172869
UR - https://www.ncbi.nlm.nih.gov/pubmed/37646355
UR - https://www.scopus.com/pages/publications/85163172869
U2 - 10.36613/tgg.1875-6832/2023.02.03
DO - 10.36613/tgg.1875-6832/2023.02.03
M3 - Article
C2 - 37646355
SN - 0167-9228
VL - 54
JO - Tijdschrift voor gerontologie en geriatrie
JF - Tijdschrift voor gerontologie en geriatrie
IS - 2
ER -