Resultados: 18

Relationship between Burden and Perceived Social Support in Low-income Caregivers Authors

Aquichan; 23 (1), 2023
Objectives: To describe and correlate burden and social support in low-income caregivers of chronic patients. Material and methods: A descriptive and cross-sectional study was conducted with 170 low-income family caregivers of people with chronic diseases who answered a survey on sociodemographic and car...

Fatores socioculturais que contribuem para a qualidade de vida de cuidadores familiares de adultos dependentes de cuidados crônicos: um estudo qualitativo no brasil

REME rev. min. enferm; 26 (), 2022
RESUMO Objetivo: explorar os fatores socioculturais que contribuem para a qualidade de vida de cuidadores familiares de adultos dependentes de cuidados crônicos no Brasil. Método: estudo qualitativo realizado de outubro de 2016 a março de 2017 em Belo Horizonte, Minas Gerais, Brasil. Vinte e cinco c...

La experiencia de los cuidadores familiares de personas con cáncer. Estudio fenomenológico

Rev. cienc. cuidad; 18 (3), 2021
Objetivo: Comprender la experiencia vivida de los cuidadores familiares de personas que padecen enfermedades oncológicas. Materiales y métodos: Estudio de enfoque cualitativo, basado en la fenomenología interpretativa. Se desarrolló en Medellín, Colombia, entre julio de 2018 y junio de 2...

Direct and Indirect Costs of Caring for Patients with Chronic Non-Communicable Diseases

Aquichan; 20 (2), 2020
ABSTRACT Objective: To determine direct and indirect non-medical costs derived from caring for patients with chronic non-communicable diseases (NCDs) in three health institutions located in the metropolitan area of Bucaramanga, Colombia. Methods: A descriptive cross-sectional study was conducted with...

Burden of informal caregivers of dependent elderlies in the community in small cities

Rev. gaúch. enferm; 41 (spe), 2020
ABSTRACT Aim: To analyze sociodemographic factors and aspects of care related to the burden of informal caregivers of dependent elderlies in the community. Methods: A cross-sectional study with 125 caregivers. Data collection was carried out in municipalities of the Northwest of Rio Grande do Sul throu...

Quality of life, burden, family emotional support: a model for older adults who are caregivers

Rev. bras. enferm; 72 (supl.2), 2019
ABSTRACT Objective: To investigate associations between quality of life, sex, age, burden, and nature of emotional support available in the family in older adults who are caregivers of older relatives. Method: Cross-sectional and correlational study on 148 caregivers gathered in public and private heal...

Caregiver burden and stress in psychiatric hospital admission

Rev. bras. enferm; 72 (6), 2019
ABSTRACT Objective: to evaluate the relation between sociodemographics factors, stress and burden of care of family caregivers of patients at a psychiatric hospital admission. Method: quantitative study, with a cross-sectional correlation design. A total of 112 family caregivers participated, older tha...

Caring for the carer: quality of life and burden of female caregivers

Rev. bras. enferm; 72 (3), 2019
ABSTRACT Objective: To assess the quality of life and the burden of female caregivers. Method: Descriptive, cross-sectional, quantitative study carried out with 224 informal caregivers from March to July 2016. Three instruments were used: a characterization form for the caregiver, the WHOQOL-Bref quest...

Illness trajectory in heart failure: narratives of family caregivers

Rev. bras. enferm; 72 (1), 2019
ABSTRACT Objective: To explore the meaning of being a family caregiver for a relative with advanced heart failure (HF) in their own home, and to gain an understanding of how dignity is upheld in family caregiving contexts. Method: We used a phenomenological-hermeneutical method inspired by the Ricoeuri...

Being caregiver of people with Parkinson's Disease: experienced situations

Rev. bras. enferm; 71 (supl.6), 2018
ABSTRACT Objective: To understand the experience of caring for a person with Parkinson's Disease. Method: We used the qualitative study and thematic analysis with family caregivers of people with Parkinson's Disease. Results: Three thematic categories were identified, being: Feelings related to Parkin...