Premium
Differences Between Dementia Caregivers Who are Users and Nonusers of Community Services
Author(s) -
Robinson Karen M.,
Buckwalter Kathleen,
Reed David
Publication year - 2013
Publication title -
public health nursing
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.471
H-Index - 55
eISSN - 1525-1446
pISSN - 0737-1209
DOI - 10.1111/phn.12041
Subject(s) - respite care , spouse , dementia , gerontology , social support , medicine , caregiver burden , public health , depression (economics) , psychology , nursing , disease , pathology , sociology , anthropology , economics , psychotherapist , macroeconomics
Objectives To examine differences between users and non‐users of community services in caregivers of persons with dementia ( PWD ). A profile of who used services versus did not use services was developed. Design and Sample Existing cross‐sectional data from the NINR funded National Caregiver Training Project (data collected 1995–1997) were used. The sample ( N = 241) of caucasian, well‐educated caregivers reflected a mix of spouse and adult caregivers with a mean age of 64.8 years. Measures Variables measured included caregiver social support, burden, and depression as well as problem behavior of PWD . Results The majority of caregivers did not attend support groups (73%) or use respite services (79%). Among caregivers who did not use services, 78% lived with the recipient and 77% were spouses. The profile of non‐users compared to users revealed that non‐users were significantly older, more depressed, and received less social support. On the other hand, non‐users provided fewer hours of care per week to recipients who had less cognitive and functional deterioration and fewer behavior problems. Conclusions These findings provide public health nurses with knowledge about service use in caregivers of PWD . Recommendations regarding caregiver needs for assistance and increased use of services before a crisis ensues are presented.