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An Assessment of Dementia Caregivers’ Interaction With Community-Based Services

Respite care is an important service to address caregivers' stress and fatigue when caring for a person with dementia (PWD). YouthCare is a non-medical, at-home, intergenerational respite care program that partners trained student volunteers with PWDs. The Family Caregiver Survey was created an...

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Autores principales: Saravanan, Deepika Pugalenthi, Satyadev, Nihal, Townsend, Natashia, Rose, Katherine, Ma, Harrison, Benton, Donna, Levy-Storms, Lené
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8681337/
http://dx.doi.org/10.1093/geroni/igab046.2819
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author Saravanan, Deepika Pugalenthi
Satyadev, Nihal
Townsend, Natashia
Rose, Katherine
Ma, Harrison
Benton, Donna
Levy-Storms, Lené
author_facet Saravanan, Deepika Pugalenthi
Satyadev, Nihal
Townsend, Natashia
Rose, Katherine
Ma, Harrison
Benton, Donna
Levy-Storms, Lené
author_sort Saravanan, Deepika Pugalenthi
collection PubMed
description Respite care is an important service to address caregivers' stress and fatigue when caring for a person with dementia (PWD). YouthCare is a non-medical, at-home, intergenerational respite care program that partners trained student volunteers with PWDs. The Family Caregiver Survey was created and distributed to caregivers of PWDs in Los Angeles to better understand interactions with the community and its caregiver services. The survey assesses caregivers’ demographics, daily activities, mental health, and the type of respite support needed. The survey findings (n=47) show that 53.2% of caregivers are 54 and older and 83% females. 40.4% of the caregivers listened to the radio primarily in the morning while 61.7% watched television in the afternoon to evening time. For transportation of PWDs to and from destinations, 78.3% of caregivers reported using their own vehicles. In regards to their mental health, 61.7% of the caregivers stated that they felt tired and unmotivated to complete daily activities. When asked why they sought respite services, 40% stated that they were overwhelmed by the responsibilities in addition to their own work. The groups that primarily support caregivers are family and professional respite services. Findings indicate that caregivers are most likely to trust resource recommendations from family and friends. Similar surveys should be administered in other cities and in rural locations to improve the generalizability of our findings.
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spelling pubmed-86813372021-12-17 An Assessment of Dementia Caregivers’ Interaction With Community-Based Services Saravanan, Deepika Pugalenthi Satyadev, Nihal Townsend, Natashia Rose, Katherine Ma, Harrison Benton, Donna Levy-Storms, Lené Innov Aging Abstracts Respite care is an important service to address caregivers' stress and fatigue when caring for a person with dementia (PWD). YouthCare is a non-medical, at-home, intergenerational respite care program that partners trained student volunteers with PWDs. The Family Caregiver Survey was created and distributed to caregivers of PWDs in Los Angeles to better understand interactions with the community and its caregiver services. The survey assesses caregivers’ demographics, daily activities, mental health, and the type of respite support needed. The survey findings (n=47) show that 53.2% of caregivers are 54 and older and 83% females. 40.4% of the caregivers listened to the radio primarily in the morning while 61.7% watched television in the afternoon to evening time. For transportation of PWDs to and from destinations, 78.3% of caregivers reported using their own vehicles. In regards to their mental health, 61.7% of the caregivers stated that they felt tired and unmotivated to complete daily activities. When asked why they sought respite services, 40% stated that they were overwhelmed by the responsibilities in addition to their own work. The groups that primarily support caregivers are family and professional respite services. Findings indicate that caregivers are most likely to trust resource recommendations from family and friends. Similar surveys should be administered in other cities and in rural locations to improve the generalizability of our findings. Oxford University Press 2021-12-17 /pmc/articles/PMC8681337/ http://dx.doi.org/10.1093/geroni/igab046.2819 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of The Gerontological Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstracts
Saravanan, Deepika Pugalenthi
Satyadev, Nihal
Townsend, Natashia
Rose, Katherine
Ma, Harrison
Benton, Donna
Levy-Storms, Lené
An Assessment of Dementia Caregivers’ Interaction With Community-Based Services
title An Assessment of Dementia Caregivers’ Interaction With Community-Based Services
title_full An Assessment of Dementia Caregivers’ Interaction With Community-Based Services
title_fullStr An Assessment of Dementia Caregivers’ Interaction With Community-Based Services
title_full_unstemmed An Assessment of Dementia Caregivers’ Interaction With Community-Based Services
title_short An Assessment of Dementia Caregivers’ Interaction With Community-Based Services
title_sort assessment of dementia caregivers’ interaction with community-based services
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8681337/
http://dx.doi.org/10.1093/geroni/igab046.2819
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