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The voices of family caregivers of seniors with chronic conditions: a window into their experience using a qualitative design
BACKGROUND: Family caregivers are the backbone of the healthcare system. Over time, caregiving takes a tremendous toll on the caregiver. This is particularly true for caregivers who (1) provide >21 h of care/week, and/or (2) support those experiencing depression, cognitive decline, aggressive beh...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4870523/ https://www.ncbi.nlm.nih.gov/pubmed/27330886 http://dx.doi.org/10.1186/s40064-016-2244-z |
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author | Brémault-Phillips, Suzette Parmar, Jasneet Johnson, Melissa Huhn, Arlene Mann, Anna Tian, Victoria Sacrey, Lori-Ann R. |
author_facet | Brémault-Phillips, Suzette Parmar, Jasneet Johnson, Melissa Huhn, Arlene Mann, Anna Tian, Victoria Sacrey, Lori-Ann R. |
author_sort | Brémault-Phillips, Suzette |
collection | PubMed |
description | BACKGROUND: Family caregivers are the backbone of the healthcare system. Over time, caregiving takes a tremendous toll on the caregiver. This is particularly true for caregivers who (1) provide >21 h of care/week, and/or (2) support those experiencing depression, cognitive decline, aggressive behaviours, and life-limiting conditions requiring complex care. Many caregivers face deteriorating physical and mental health, social isolation, family conflict, and job loss. Caregivers often have little energy or time to access resources and their experiences with the healthcare system, healthcare professionals and service agencies can either buoy them through challenging times, or contribute further to their distress. OBJECTIVE: This project aimed to hear the voices of family caregivers; their challenges, struggles, joys, and motivation for persevering through hardship, as well as their recommendations regarding education, resources, and supports that might enhance their resilience. METHODS: This community engagement research project utilized an ethnographic, qualitative approach involving three, 2-h focus groups that were analyzed using thematic analysis. FINDINGS: Caregivers identified barriers to resilience, including demands on their time, changing roles and responsibilities, challenges of learning about medical conditions, their own emotional responses, financial strains, changing family dynamics, and personal health. Caregivers also identified several facilitators to resilience, including motivations for caregiving, sense of purpose and validation, spirituality, emotional experiences, and coping strategies. CONCLUSION: Caregivers recommended that educational opportunities, including increasing health care providers education concerning dementias, increased access to resources, system navigators, financial supports, political advocacy, and a more responsive caregiver centered system would support family caregiving. |
format | Online Article Text |
id | pubmed-4870523 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-48705232016-06-21 The voices of family caregivers of seniors with chronic conditions: a window into their experience using a qualitative design Brémault-Phillips, Suzette Parmar, Jasneet Johnson, Melissa Huhn, Arlene Mann, Anna Tian, Victoria Sacrey, Lori-Ann R. Springerplus Research BACKGROUND: Family caregivers are the backbone of the healthcare system. Over time, caregiving takes a tremendous toll on the caregiver. This is particularly true for caregivers who (1) provide >21 h of care/week, and/or (2) support those experiencing depression, cognitive decline, aggressive behaviours, and life-limiting conditions requiring complex care. Many caregivers face deteriorating physical and mental health, social isolation, family conflict, and job loss. Caregivers often have little energy or time to access resources and their experiences with the healthcare system, healthcare professionals and service agencies can either buoy them through challenging times, or contribute further to their distress. OBJECTIVE: This project aimed to hear the voices of family caregivers; their challenges, struggles, joys, and motivation for persevering through hardship, as well as their recommendations regarding education, resources, and supports that might enhance their resilience. METHODS: This community engagement research project utilized an ethnographic, qualitative approach involving three, 2-h focus groups that were analyzed using thematic analysis. FINDINGS: Caregivers identified barriers to resilience, including demands on their time, changing roles and responsibilities, challenges of learning about medical conditions, their own emotional responses, financial strains, changing family dynamics, and personal health. Caregivers also identified several facilitators to resilience, including motivations for caregiving, sense of purpose and validation, spirituality, emotional experiences, and coping strategies. CONCLUSION: Caregivers recommended that educational opportunities, including increasing health care providers education concerning dementias, increased access to resources, system navigators, financial supports, political advocacy, and a more responsive caregiver centered system would support family caregiving. Springer International Publishing 2016-05-14 /pmc/articles/PMC4870523/ /pubmed/27330886 http://dx.doi.org/10.1186/s40064-016-2244-z Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Research Brémault-Phillips, Suzette Parmar, Jasneet Johnson, Melissa Huhn, Arlene Mann, Anna Tian, Victoria Sacrey, Lori-Ann R. The voices of family caregivers of seniors with chronic conditions: a window into their experience using a qualitative design |
title | The voices of family caregivers of seniors with chronic conditions: a window into their experience using a qualitative design |
title_full | The voices of family caregivers of seniors with chronic conditions: a window into their experience using a qualitative design |
title_fullStr | The voices of family caregivers of seniors with chronic conditions: a window into their experience using a qualitative design |
title_full_unstemmed | The voices of family caregivers of seniors with chronic conditions: a window into their experience using a qualitative design |
title_short | The voices of family caregivers of seniors with chronic conditions: a window into their experience using a qualitative design |
title_sort | voices of family caregivers of seniors with chronic conditions: a window into their experience using a qualitative design |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4870523/ https://www.ncbi.nlm.nih.gov/pubmed/27330886 http://dx.doi.org/10.1186/s40064-016-2244-z |
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