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Peer support meeting of people with dementia: a qualitative descriptive analysis of the discussions
BACKGROUND: Dementia cafés for people with dementia and their caregivers are promoted in national dementia policies. The effect of dementia cafés on people with dementia has been reported through narratives of caregivers who participated the dementia cafés. However, evidence derived from the data, w...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10563253/ https://www.ncbi.nlm.nih.gov/pubmed/37814249 http://dx.doi.org/10.1186/s12877-023-04329-8 |
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author | Miyamae, Fumiko Sugiyama, Mika Taga, Tsutomu Okamura, Tsuyoshi |
author_facet | Miyamae, Fumiko Sugiyama, Mika Taga, Tsutomu Okamura, Tsuyoshi |
author_sort | Miyamae, Fumiko |
collection | PubMed |
description | BACKGROUND: Dementia cafés for people with dementia and their caregivers are promoted in national dementia policies. The effect of dementia cafés on people with dementia has been reported through narratives of caregivers who participated the dementia cafés. However, evidence derived from the data, which included only people with dementia, is sparse. The aim of this study is to analyze the narratives of people with dementia in peer support meetings in Tokyo where only people with dementia participate, i.e., caregivers were not present. METHODS: People with dementia and older people with subjective cognitive impairment were recruited in our community-based participatory research centre. Based on the qualitative descriptive approach, we conducted a thematic analysis of the field notes, which was made through ethnographical observation of the meetings. RESULTS: Twenty-five meetings were held from November 2018 to March 2020. The cumulative total number of participants was 196. First, the symptomatic problems related to living with dementia were mentioned, which were collectively named under the overarching category of ‘Experience of living with dementia.’ Second, questions and solutions to the various symptoms were discussed, which were named the ‘Quest of Symptoms.’ Third, we noted the narrative that reflected on daily life, feelings, and the life that one has led, which were named ‘Life story.’ Fourth, we noted narratives of how symptoms have improved and their world has expanded, which were named ‘Hope.’ Fifth and most importantly, narratives about compassion for people with dementia in the past and future, as well as for people of the same generation, were discussed, which were named ‘Compassion.’ CONCLUSIONS: The lived experiences of people with dementia were revealed. Participants noted they were not just being cared for but exchanging information and exploring the symptoms; in other words, they were resilient. Furthermore, more positive aspects concerning living with dementia were discussed, such as ‘Hope’ and ‘Compassion.’ Further research concerning the discourse of people around the participants is necessary to evaluate the situation from multiple perspectives. |
format | Online Article Text |
id | pubmed-10563253 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-105632532023-10-11 Peer support meeting of people with dementia: a qualitative descriptive analysis of the discussions Miyamae, Fumiko Sugiyama, Mika Taga, Tsutomu Okamura, Tsuyoshi BMC Geriatr Research BACKGROUND: Dementia cafés for people with dementia and their caregivers are promoted in national dementia policies. The effect of dementia cafés on people with dementia has been reported through narratives of caregivers who participated the dementia cafés. However, evidence derived from the data, which included only people with dementia, is sparse. The aim of this study is to analyze the narratives of people with dementia in peer support meetings in Tokyo where only people with dementia participate, i.e., caregivers were not present. METHODS: People with dementia and older people with subjective cognitive impairment were recruited in our community-based participatory research centre. Based on the qualitative descriptive approach, we conducted a thematic analysis of the field notes, which was made through ethnographical observation of the meetings. RESULTS: Twenty-five meetings were held from November 2018 to March 2020. The cumulative total number of participants was 196. First, the symptomatic problems related to living with dementia were mentioned, which were collectively named under the overarching category of ‘Experience of living with dementia.’ Second, questions and solutions to the various symptoms were discussed, which were named the ‘Quest of Symptoms.’ Third, we noted the narrative that reflected on daily life, feelings, and the life that one has led, which were named ‘Life story.’ Fourth, we noted narratives of how symptoms have improved and their world has expanded, which were named ‘Hope.’ Fifth and most importantly, narratives about compassion for people with dementia in the past and future, as well as for people of the same generation, were discussed, which were named ‘Compassion.’ CONCLUSIONS: The lived experiences of people with dementia were revealed. Participants noted they were not just being cared for but exchanging information and exploring the symptoms; in other words, they were resilient. Furthermore, more positive aspects concerning living with dementia were discussed, such as ‘Hope’ and ‘Compassion.’ Further research concerning the discourse of people around the participants is necessary to evaluate the situation from multiple perspectives. BioMed Central 2023-10-09 /pmc/articles/PMC10563253/ /pubmed/37814249 http://dx.doi.org/10.1186/s12877-023-04329-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Miyamae, Fumiko Sugiyama, Mika Taga, Tsutomu Okamura, Tsuyoshi Peer support meeting of people with dementia: a qualitative descriptive analysis of the discussions |
title | Peer support meeting of people with dementia: a qualitative descriptive analysis of the discussions |
title_full | Peer support meeting of people with dementia: a qualitative descriptive analysis of the discussions |
title_fullStr | Peer support meeting of people with dementia: a qualitative descriptive analysis of the discussions |
title_full_unstemmed | Peer support meeting of people with dementia: a qualitative descriptive analysis of the discussions |
title_short | Peer support meeting of people with dementia: a qualitative descriptive analysis of the discussions |
title_sort | peer support meeting of people with dementia: a qualitative descriptive analysis of the discussions |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10563253/ https://www.ncbi.nlm.nih.gov/pubmed/37814249 http://dx.doi.org/10.1186/s12877-023-04329-8 |
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