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Developing a core outcome set for people living with dementia at home in their neighbourhoods and communities: study protocol for use in the evaluation of non-pharmacological community-based health and social care interventions

BACKGROUND: The key aim of the study is to establish an agreed standardised core outcome set (COS) for use when evaluating non-pharmacological health and social care interventions for people living at home with dementia. METHODS/DESIGN: Drawing on the guidance and approaches of the Core Outcome Meas...

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Autores principales: Harding, Andrew J. E., Morbey, Hazel, Ahmed, Faraz, Opdebeeck, Carol, Wang, Ying-Ying, Williamson, Paula, Swarbrick, Caroline, Leroi, Iracema, Challis, David, Davies, Linda, Reeves, David, Holland, Fiona, Hann, Mark, Hellström, Ingrid, Hydén, Lars-Christer, Burns, Alistair, Keady, John, Reilly, Siobhan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5916721/
https://www.ncbi.nlm.nih.gov/pubmed/29690920
http://dx.doi.org/10.1186/s13063-018-2584-9
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author Harding, Andrew J. E.
Morbey, Hazel
Ahmed, Faraz
Opdebeeck, Carol
Wang, Ying-Ying
Williamson, Paula
Swarbrick, Caroline
Leroi, Iracema
Challis, David
Davies, Linda
Reeves, David
Holland, Fiona
Hann, Mark
Hellström, Ingrid
Hydén, Lars-Christer
Burns, Alistair
Keady, John
Reilly, Siobhan
author_facet Harding, Andrew J. E.
Morbey, Hazel
Ahmed, Faraz
Opdebeeck, Carol
Wang, Ying-Ying
Williamson, Paula
Swarbrick, Caroline
Leroi, Iracema
Challis, David
Davies, Linda
Reeves, David
Holland, Fiona
Hann, Mark
Hellström, Ingrid
Hydén, Lars-Christer
Burns, Alistair
Keady, John
Reilly, Siobhan
author_sort Harding, Andrew J. E.
collection PubMed
description BACKGROUND: The key aim of the study is to establish an agreed standardised core outcome set (COS) for use when evaluating non-pharmacological health and social care interventions for people living at home with dementia. METHODS/DESIGN: Drawing on the guidance and approaches of the Core Outcome Measures in Effectiveness Trials (COMET), this study uses a four-phase mixed-methods design: 1. Focus groups and interviews with key stakeholder groups (people living with dementia, care partners, relevant health and social care professionals, researchers and policymakers) and a review of the literature will be undertaken to build a long list of outcomes. 2. Two rounds of Delphi surveys will be used with key stakeholder groups. Statements for the Delphi surveys and participation processes will be developed and informed through substantial member involvement with people living with dementia and care partners. A consensus meeting will be convened with key participant groups to discuss the key findings and finalise the COS. 3. A systematic literature review will be undertaken to assess the properties of tools and instruments to assess components of the COS. Measurement properties, validity and reliability will be assessed using the Consensus-based Standards for the Selection of Health Measurement (COSMIN) and COMET guidance. 4. A stated preference survey will elicit the preferences of key stakeholders for the outcomes identified as important to measure in the COS. DISCUSSION: To the best of our knowledge, this study is the first to use a modified Delphi process to involve people living with dementia as a participant group. Though the study is confined to collecting data in the United Kingdom, use of the COS by researchers will enhance the comparability of studies evaluating non-pharmacological and community-based interventions. TRIAL REGISTRATION: The study is registered on the COMET initiative, registered in 2014 at comet-initiative.org. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13063-018-2584-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-59167212018-04-30 Developing a core outcome set for people living with dementia at home in their neighbourhoods and communities: study protocol for use in the evaluation of non-pharmacological community-based health and social care interventions Harding, Andrew J. E. Morbey, Hazel Ahmed, Faraz Opdebeeck, Carol Wang, Ying-Ying Williamson, Paula Swarbrick, Caroline Leroi, Iracema Challis, David Davies, Linda Reeves, David Holland, Fiona Hann, Mark Hellström, Ingrid Hydén, Lars-Christer Burns, Alistair Keady, John Reilly, Siobhan Trials Study Protocol BACKGROUND: The key aim of the study is to establish an agreed standardised core outcome set (COS) for use when evaluating non-pharmacological health and social care interventions for people living at home with dementia. METHODS/DESIGN: Drawing on the guidance and approaches of the Core Outcome Measures in Effectiveness Trials (COMET), this study uses a four-phase mixed-methods design: 1. Focus groups and interviews with key stakeholder groups (people living with dementia, care partners, relevant health and social care professionals, researchers and policymakers) and a review of the literature will be undertaken to build a long list of outcomes. 2. Two rounds of Delphi surveys will be used with key stakeholder groups. Statements for the Delphi surveys and participation processes will be developed and informed through substantial member involvement with people living with dementia and care partners. A consensus meeting will be convened with key participant groups to discuss the key findings and finalise the COS. 3. A systematic literature review will be undertaken to assess the properties of tools and instruments to assess components of the COS. Measurement properties, validity and reliability will be assessed using the Consensus-based Standards for the Selection of Health Measurement (COSMIN) and COMET guidance. 4. A stated preference survey will elicit the preferences of key stakeholders for the outcomes identified as important to measure in the COS. DISCUSSION: To the best of our knowledge, this study is the first to use a modified Delphi process to involve people living with dementia as a participant group. Though the study is confined to collecting data in the United Kingdom, use of the COS by researchers will enhance the comparability of studies evaluating non-pharmacological and community-based interventions. TRIAL REGISTRATION: The study is registered on the COMET initiative, registered in 2014 at comet-initiative.org. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13063-018-2584-9) contains supplementary material, which is available to authorized users. BioMed Central 2018-04-24 /pmc/articles/PMC5916721/ /pubmed/29690920 http://dx.doi.org/10.1186/s13063-018-2584-9 Text en © The Author(s). 2018 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 Study Protocol
Harding, Andrew J. E.
Morbey, Hazel
Ahmed, Faraz
Opdebeeck, Carol
Wang, Ying-Ying
Williamson, Paula
Swarbrick, Caroline
Leroi, Iracema
Challis, David
Davies, Linda
Reeves, David
Holland, Fiona
Hann, Mark
Hellström, Ingrid
Hydén, Lars-Christer
Burns, Alistair
Keady, John
Reilly, Siobhan
Developing a core outcome set for people living with dementia at home in their neighbourhoods and communities: study protocol for use in the evaluation of non-pharmacological community-based health and social care interventions
title Developing a core outcome set for people living with dementia at home in their neighbourhoods and communities: study protocol for use in the evaluation of non-pharmacological community-based health and social care interventions
title_full Developing a core outcome set for people living with dementia at home in their neighbourhoods and communities: study protocol for use in the evaluation of non-pharmacological community-based health and social care interventions
title_fullStr Developing a core outcome set for people living with dementia at home in their neighbourhoods and communities: study protocol for use in the evaluation of non-pharmacological community-based health and social care interventions
title_full_unstemmed Developing a core outcome set for people living with dementia at home in their neighbourhoods and communities: study protocol for use in the evaluation of non-pharmacological community-based health and social care interventions
title_short Developing a core outcome set for people living with dementia at home in their neighbourhoods and communities: study protocol for use in the evaluation of non-pharmacological community-based health and social care interventions
title_sort developing a core outcome set for people living with dementia at home in their neighbourhoods and communities: study protocol for use in the evaluation of non-pharmacological community-based health and social care interventions
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5916721/
https://www.ncbi.nlm.nih.gov/pubmed/29690920
http://dx.doi.org/10.1186/s13063-018-2584-9
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