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Social and psychological impact of the COVID-19 pandemic on people with Parkinson's disease: a scoping review

OBJECTIVES: The COVID-19 pandemic caused countries across the globe to impose restrictions to slow the spread of the virus, with people instructed to stay at home and reduce contact with others. This reduction in social contact has the potential to negatively impact mental health and well-being. The...

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Autores principales: Brooks, S.K., Weston, D., Greenberg, N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society for Public Health. Published by Elsevier Ltd. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8407946/
https://www.ncbi.nlm.nih.gov/pubmed/34571441
http://dx.doi.org/10.1016/j.puhe.2021.08.014
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author Brooks, S.K.
Weston, D.
Greenberg, N.
author_facet Brooks, S.K.
Weston, D.
Greenberg, N.
author_sort Brooks, S.K.
collection PubMed
description OBJECTIVES: The COVID-19 pandemic caused countries across the globe to impose restrictions to slow the spread of the virus, with people instructed to stay at home and reduce contact with others. This reduction in social contact has the potential to negatively impact mental health and well-being. The restrictions are particularly concerning for people with existing chronic illnesses such as Parkinson's disease, who may be especially affected by concerns about the pandemic and associated reduction of social contact. The aim of this review was to synthesise published literature on the impact of the COVID-19 pandemic on the social and psychological well-being of people with Parkinson's disease. STUDY DESIGN: The design of this study is a scoping review. METHODS: We searched five electronic databases for English language articles containing primary data on this topic. RESULTS: Thirty-one relevant studies were found and included in the review. Six main themes were identified: impact of the pandemic on physical and mental health; COVID-19 concerns; access to health care; impact on daily and social activities; impact on physical activity and impact on caregivers. Levels of perceived risk of COVID-19 differed across studies, but most participants had adopted preventive measures such as staying at home and reducing social contacts. Participants in many studies reported a discontinuation of regular healthcare appointments and physiotherapy, as well as concerns about being able to obtain medication. Loss of daily activities and social support was noted by many participants. There was mixed evidence on the impact of the pandemic on physical exercise, with some studies finding no change in physical activity and others reporting a reduction; generally, participants with reduced physical activity had poorer mental health and greater worsening of symptoms. Caregivers of people with Parkinson's disease were more likely to be negatively affected by the pandemic if they cared for people with complex needs such as additional mental health problems. CONCLUSIONS: The COVID-19 pandemic has had negative effects on the physical and mental health of people with Parkinson's disease, perhaps due to disruption of healthcare services, loss of usual activities and supports and reduction in physical activity. We make recommendations for policy, practice and future research.
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spelling pubmed-84079462021-09-01 Social and psychological impact of the COVID-19 pandemic on people with Parkinson's disease: a scoping review Brooks, S.K. Weston, D. Greenberg, N. Public Health Review Paper OBJECTIVES: The COVID-19 pandemic caused countries across the globe to impose restrictions to slow the spread of the virus, with people instructed to stay at home and reduce contact with others. This reduction in social contact has the potential to negatively impact mental health and well-being. The restrictions are particularly concerning for people with existing chronic illnesses such as Parkinson's disease, who may be especially affected by concerns about the pandemic and associated reduction of social contact. The aim of this review was to synthesise published literature on the impact of the COVID-19 pandemic on the social and psychological well-being of people with Parkinson's disease. STUDY DESIGN: The design of this study is a scoping review. METHODS: We searched five electronic databases for English language articles containing primary data on this topic. RESULTS: Thirty-one relevant studies were found and included in the review. Six main themes were identified: impact of the pandemic on physical and mental health; COVID-19 concerns; access to health care; impact on daily and social activities; impact on physical activity and impact on caregivers. Levels of perceived risk of COVID-19 differed across studies, but most participants had adopted preventive measures such as staying at home and reducing social contacts. Participants in many studies reported a discontinuation of regular healthcare appointments and physiotherapy, as well as concerns about being able to obtain medication. Loss of daily activities and social support was noted by many participants. There was mixed evidence on the impact of the pandemic on physical exercise, with some studies finding no change in physical activity and others reporting a reduction; generally, participants with reduced physical activity had poorer mental health and greater worsening of symptoms. Caregivers of people with Parkinson's disease were more likely to be negatively affected by the pandemic if they cared for people with complex needs such as additional mental health problems. CONCLUSIONS: The COVID-19 pandemic has had negative effects on the physical and mental health of people with Parkinson's disease, perhaps due to disruption of healthcare services, loss of usual activities and supports and reduction in physical activity. We make recommendations for policy, practice and future research. The Royal Society for Public Health. Published by Elsevier Ltd. 2021-10 2021-09-01 /pmc/articles/PMC8407946/ /pubmed/34571441 http://dx.doi.org/10.1016/j.puhe.2021.08.014 Text en © 2021 The Royal Society for Public Health. Published by Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Review Paper
Brooks, S.K.
Weston, D.
Greenberg, N.
Social and psychological impact of the COVID-19 pandemic on people with Parkinson's disease: a scoping review
title Social and psychological impact of the COVID-19 pandemic on people with Parkinson's disease: a scoping review
title_full Social and psychological impact of the COVID-19 pandemic on people with Parkinson's disease: a scoping review
title_fullStr Social and psychological impact of the COVID-19 pandemic on people with Parkinson's disease: a scoping review
title_full_unstemmed Social and psychological impact of the COVID-19 pandemic on people with Parkinson's disease: a scoping review
title_short Social and psychological impact of the COVID-19 pandemic on people with Parkinson's disease: a scoping review
title_sort social and psychological impact of the covid-19 pandemic on people with parkinson's disease: a scoping review
topic Review Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8407946/
https://www.ncbi.nlm.nih.gov/pubmed/34571441
http://dx.doi.org/10.1016/j.puhe.2021.08.014
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