Identity, relationship quality, and subjective burden in caregivers of persons with dementia

Author:

Enright Joe1,O’Connell Megan E1,Branger Camille1,Kirk Andrew1,Morgan Debra1

Affiliation:

1. University of Saskatchewan, Canada

Abstract

The aim of the current study was to examine the associations between informal caregivers’ perception of identity change in their care-partner, the quality of the caregiver/care-recipient relationship, and caregiver burden in a sample of 56 informal caregivers of persons with dementia. Most (96.4%) of the caregivers of persons who received a dementia diagnosis reported a perceived change in the identity of their care-partner. Caregivers’ perception of relationship satisfaction was measured with the Burns Relationship Satisfaction Scale for premorbid relationship and current relationship quality, and caregiver burden was measured with the Zarit Burden scale. After controlling for variance due to dementia severity, premorbid relationship satisfaction, and current relationship satisfaction, caregivers’ perceived change in the identity of the person with dementia accounted for significant variance in caregiver burden. Using a mediational model, we found support for a direct effect between perceived change in identity and caregiver burden, but we also found support for an indirect effect of relationship quality on the relation between perceived identity change and caregiver burden. The demonstrated model provides an empirically supported theoretical framework for guiding potential research and development of future interventions, which we suggest should emphasize dyads.

Funder

Canadian Institutes of Health Research

Saskatchewan Health Research Foundation

Alzheimer Society

Canadian Frailty Network

Publisher

SAGE Publications

Subject

General Social Sciences,Sociology and Political Science,General Medicine

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