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“You have to know why you're doing this”: a mixed methods study of the benefits and burdens of self-tracking in Parkinson's disease
BACKGROUND: This study explores opinions and experiences of people with Parkinson’s disease (PwP) in Sweden of using self-tracking. Parkinson’s disease (PD) is a neurodegenerative condition entailing varied and changing symptoms and side effects that can be a challenge to manage optimally. Patients’...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6716928/ https://www.ncbi.nlm.nih.gov/pubmed/31470832 http://dx.doi.org/10.1186/s12911-019-0896-7 |
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author | Riggare, Sara Scott Duncan, Therese Hvitfeldt, Helena Hägglund, Maria |
author_facet | Riggare, Sara Scott Duncan, Therese Hvitfeldt, Helena Hägglund, Maria |
author_sort | Riggare, Sara |
collection | PubMed |
description | BACKGROUND: This study explores opinions and experiences of people with Parkinson’s disease (PwP) in Sweden of using self-tracking. Parkinson’s disease (PD) is a neurodegenerative condition entailing varied and changing symptoms and side effects that can be a challenge to manage optimally. Patients’ self-tracking has demonstrated potential in other diseases, but we know little about PD self-tracking. The aim of this study was therefore to explore the opinions and experiences of PwP in Sweden of using self-tracking for PD. METHOD: A mixed methods approach was used, combining qualitative data from seven interviews with quantitative data from a survey to formulate a model for self-tracking in PD. In total 280 PwP responded to the survey, 64% (n = 180) of which had experience from self-tracking. RESULT: We propose a model for self-tracking in PD which share distinctive characteristics with the Plan-Do-Study-Act (PDSA) cycle for healthcare improvement. PwP think that tracking takes a lot of work and the right individual balance between burdens and benefits needs to be found. Some strategies have here been identified; to focus on positive aspects rather than negative, to find better solutions for their selfcare, and to increase the benefits through improved tools and increased use of self-tracking results in the dialogue with healthcare. CONCLUSION: The main identified benefits are that self-tracking gives PwP a deeper understanding of their own specific manifestations of PD and contributes to a more effective decision making regarding their own selfcare. The process of self-tracking also enables PwP to be more active in communicating with healthcare. Tracking takes a lot of work and there is a need to find the right balance between burdens and benefits. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12911-019-0896-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6716928 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-67169282019-09-04 “You have to know why you're doing this”: a mixed methods study of the benefits and burdens of self-tracking in Parkinson's disease Riggare, Sara Scott Duncan, Therese Hvitfeldt, Helena Hägglund, Maria BMC Med Inform Decis Mak Research Article BACKGROUND: This study explores opinions and experiences of people with Parkinson’s disease (PwP) in Sweden of using self-tracking. Parkinson’s disease (PD) is a neurodegenerative condition entailing varied and changing symptoms and side effects that can be a challenge to manage optimally. Patients’ self-tracking has demonstrated potential in other diseases, but we know little about PD self-tracking. The aim of this study was therefore to explore the opinions and experiences of PwP in Sweden of using self-tracking for PD. METHOD: A mixed methods approach was used, combining qualitative data from seven interviews with quantitative data from a survey to formulate a model for self-tracking in PD. In total 280 PwP responded to the survey, 64% (n = 180) of which had experience from self-tracking. RESULT: We propose a model for self-tracking in PD which share distinctive characteristics with the Plan-Do-Study-Act (PDSA) cycle for healthcare improvement. PwP think that tracking takes a lot of work and the right individual balance between burdens and benefits needs to be found. Some strategies have here been identified; to focus on positive aspects rather than negative, to find better solutions for their selfcare, and to increase the benefits through improved tools and increased use of self-tracking results in the dialogue with healthcare. CONCLUSION: The main identified benefits are that self-tracking gives PwP a deeper understanding of their own specific manifestations of PD and contributes to a more effective decision making regarding their own selfcare. The process of self-tracking also enables PwP to be more active in communicating with healthcare. Tracking takes a lot of work and there is a need to find the right balance between burdens and benefits. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12911-019-0896-7) contains supplementary material, which is available to authorized users. BioMed Central 2019-08-30 /pmc/articles/PMC6716928/ /pubmed/31470832 http://dx.doi.org/10.1186/s12911-019-0896-7 Text en © The Author(s). 2019 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Riggare, Sara Scott Duncan, Therese Hvitfeldt, Helena Hägglund, Maria “You have to know why you're doing this”: a mixed methods study of the benefits and burdens of self-tracking in Parkinson's disease |
title | “You have to know why you're doing this”: a mixed methods study of the benefits and burdens of self-tracking in Parkinson's disease |
title_full | “You have to know why you're doing this”: a mixed methods study of the benefits and burdens of self-tracking in Parkinson's disease |
title_fullStr | “You have to know why you're doing this”: a mixed methods study of the benefits and burdens of self-tracking in Parkinson's disease |
title_full_unstemmed | “You have to know why you're doing this”: a mixed methods study of the benefits and burdens of self-tracking in Parkinson's disease |
title_short | “You have to know why you're doing this”: a mixed methods study of the benefits and burdens of self-tracking in Parkinson's disease |
title_sort | “you have to know why you're doing this”: a mixed methods study of the benefits and burdens of self-tracking in parkinson's disease |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6716928/ https://www.ncbi.nlm.nih.gov/pubmed/31470832 http://dx.doi.org/10.1186/s12911-019-0896-7 |
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