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ABSTRACT: Aims and objectives
To explore reflections of family caregivers and health professionals regarding the challenges involved in caring for persons with amyotrophic lateral sclerosis and cognitive and/or behavioral impairments (PALS/CIs).Background
Family caregivers of PALS/CIs are highly burdened and at great risk of psychological sequela. Professionals working with these families can be negatively affected on their well-being and are at risk of burnout.Design
The design was a qualitative interview study.Methods
One focus group and 10 individual semi-structured interviews were conducted with seven family caregivers and nine professionals after the death of a PALS/CIs. The analysis was guided by the interpretive description methodology and the theory of sense o
SUBMITTER: Olesen LK
PROVIDER: S-EPMC8855464 | biostudies-literature | 2022
REPOSITORIES: biostudies-literature