TY - JOUR
T1 - Changes in caregiving appraisal among family caregivers of persons with dementia
T2 - A longitudinal study over 12 months
AU - Kajiwara, Kohei
AU - Noto, Hiroko
AU - Yamanaka, Makoto
N1 - Funding Information:
This study was supported by JSPS KAKENHI (grant no. JP26861953). The authors are thankful to the cooperating facilities and family caregivers who responded to the survey.
Publisher Copyright:
© 2018 Japanese Psychogeriatric Society
PY - 2018/11
Y1 - 2018/11
N2 - Aim: The main purpose of this study was to identify changes in both caregiver burden and positive caregiving appraisal over time, as well as factors affecting these variables. Methods: This analysis included 41 in-home family caregivers who had completed questionnaires at baseline, 6 months, and 12 months. We assessed various caregiver and care recipient characteristics, caregivers’ positive appraisal of caregiving, caregiver burden, desire to continue caregiving, severity of care recipients’ cognitive impairment, and behavioural and psychological symptoms of dementia. Results: We observed no significant differences in caregiver burden, positive caregiving appraisal, or behavioural and psychological symptoms of dementia across the three measurement times. However, we did find differences in the desire to continue caregiving and in the personal strain and role strain dimensions of caregiver burden. Conclusion: Overall, our study suggests that caregiving service providers should consider support that focuses on improving the subjective caregiving appraisals of caregivers.
AB - Aim: The main purpose of this study was to identify changes in both caregiver burden and positive caregiving appraisal over time, as well as factors affecting these variables. Methods: This analysis included 41 in-home family caregivers who had completed questionnaires at baseline, 6 months, and 12 months. We assessed various caregiver and care recipient characteristics, caregivers’ positive appraisal of caregiving, caregiver burden, desire to continue caregiving, severity of care recipients’ cognitive impairment, and behavioural and psychological symptoms of dementia. Results: We observed no significant differences in caregiver burden, positive caregiving appraisal, or behavioural and psychological symptoms of dementia across the three measurement times. However, we did find differences in the desire to continue caregiving and in the personal strain and role strain dimensions of caregiver burden. Conclusion: Overall, our study suggests that caregiving service providers should consider support that focuses on improving the subjective caregiving appraisals of caregivers.
UR - http://www.scopus.com/inward/record.url?scp=85051104993&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85051104993&partnerID=8YFLogxK
U2 - 10.1111/psyg.12360
DO - 10.1111/psyg.12360
M3 - Article
C2 - 30066482
AN - SCOPUS:85051104993
VL - 18
SP - 460
EP - 467
JO - Psychogeriatrics
JF - Psychogeriatrics
SN - 1346-3500
IS - 6
ER -