Caregivers of family members with dementia described the experience of quality respite as a 3 phase cognitive journey towards a sense of “being free”
QUESTION: How do caregivers of family members with dementia experience respite?
Qualitative interpretive approach.
Edmonton, Alberta, Canada.
10 white caregivers (8 wives, 1 husband, and 1 son) who were 47–82 years of age (mean age 70 y) were recruited from self help groups, informal community connections, and home care agencies. 9 of the caregivers were retired, and the duration of caregiving ranged from 6 months to 10 years (mean 5 y). 6 of the care recipients had Alzheimer's-type dementia and 4 had multi-infarct dementia associated with stroke.
Data saturation determined the number of caregivers interviewed. Each caregiver participated in 2 indepth, loosely structured, 60–90 minute interviews (2 months apart) to discuss their experiences of caregiving and respite. Data analysis procedures included substantive coding, memoing, and integrative diagramming. Credibility was established by 2 other researchers verifying the analytical codes and emerging themes. During the second interview, caregivers verified the authenticity of the analyses by confirming and reinterpreting the researchers' findings.