Care for people with psychological distress and its repercussions on the family
Abstract
Objective: to understand how the daily care of people in psychological distress affects the life of the family caregiver and to measure the level of caregiver burden. Method: this is an exploratory and descriptive study with a mixed approach. Data was collected using a semistructured interview and the Zarit Burden Interview with 15 family members of people in psychological distress who were followed up at a CAPS III unit in a city in the metropolitan region of Salvador. Data were collected between February and August 2021, organized and analyzed using the Thematic Content Analysis technique and discussed based on existing literature. Results: the correlation of the variables revealed the level of objective and subjective burden, in addition to the feelings expressed by these family members. Six family members had moderate to severe burden according to the ZBI scale, with scores ranging from 43 to 54. The units of meaning gave rise to three thematic categories, which were presented in the infographic and illustrate how the daily care of people with psychological distress affects the lives of family caregivers. Final considerations: the study revealed that care for people in psychological distress has been carried out mainly by black women, reflecting gender and race inequalities, and that this care involves ambivalent feelings and expectations, varying levels of burden, and the need for social and state support.
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References
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