Prioritising target non-pharmacological interventions for research in Parkinson’s disease: achieving consensus from key stakeholders

Abstract Background In 2014 Parkinson’s UK conducted a research prioritisation exercise with stakeholders highlighting important clinical research questions. The exercise highlighted the need for effective interventions to be developed and tested to tackle a range of non-motor symptoms including: sl...

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Main Authors: Angeliki Bogosian, Lorna Rixon, Catherine S. Hurt
Format: Article
Language:English
Published: BMC 2020-06-01
Series:Research Involvement and Engagement
Subjects:
Online Access:http://link.springer.com/article/10.1186/s40900-020-00212-7
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spelling doaj-e6377335a2be492bbd4c30729bfc42eb2020-11-25T03:29:44ZengBMCResearch Involvement and Engagement2056-75292020-06-01611910.1186/s40900-020-00212-7Prioritising target non-pharmacological interventions for research in Parkinson’s disease: achieving consensus from key stakeholdersAngeliki Bogosian0Lorna Rixon1Catherine S. Hurt2Division of Health Services Research and Management, City, University of LondonDivision of Health Services Research and Management, City, University of LondonDivision of Health Services Research and Management, City, University of LondonAbstract Background In 2014 Parkinson’s UK conducted a research prioritisation exercise with stakeholders highlighting important clinical research questions. The exercise highlighted the need for effective interventions to be developed and tested to tackle a range of non-motor symptoms including: sleep quality, stress and anxiety, mild cognitive impairment, dementia and urinary problems. The present work set out to build on this exercise by prioritising types of non-pharmacological interventions to be tested to treat the identified non-motor symptoms. Methods A Patient and Public Involvement exercise was used to reach consensus on intervention priorities for the treatment of non-motor symptoms. A Delphi structure was used to support the feedback collected. A first-round prioritisation survey was conducted followed by a panel discussion. Nineteen panellists completed the first-round survey (9 people with Parkinson’s and 10 professionals working in Parkinson’s) and 16 participated in the panel discussion (8 people with Parkinson’s and 8 professionals working in Parkinson’s). A second-round prioritization survey was conducted after the panel discussion with 13 people with Parkinson’s. Results Physical activity, third wave cognitive therapies and cognitive training were rated as priority interventions for the treatment of a range of non-motor symptoms. There was broad agreement on intervention priorities between health care professionals and people with Parkinson’s. A consensus was reached that research should focus on therapies which could be used to treat several different non-motor symptoms. In the context of increasing digitisation, the need for human interaction as an intervention component was highlighted. Conclusion Bringing together Parkinson’s professionals and people with Parkinson’s resulted in a final treatment priority list which should be both feasible to carry out in routine clinical practice and acceptable to both professionals and people with Parkinson’s. The workshop further specified research priorities in Parkinson’s disease based on the current evidence base, stakeholder preferences, and feasibility. Research should focus on developing and testing non-pharmacological treatments which could be effective across a range of symptoms but specifically focusing on tailored physical activity interventions, cognitive therapies and cognitive training.http://link.springer.com/article/10.1186/s40900-020-00212-7Parkinson’s diseaseResearch prioritisationPublic and patient involvementResearch engagementIntervention developmentSelf-management
collection DOAJ
language English
format Article
sources DOAJ
author Angeliki Bogosian
Lorna Rixon
Catherine S. Hurt
spellingShingle Angeliki Bogosian
Lorna Rixon
Catherine S. Hurt
Prioritising target non-pharmacological interventions for research in Parkinson’s disease: achieving consensus from key stakeholders
Research Involvement and Engagement
Parkinson’s disease
Research prioritisation
Public and patient involvement
Research engagement
Intervention development
Self-management
author_facet Angeliki Bogosian
Lorna Rixon
Catherine S. Hurt
author_sort Angeliki Bogosian
title Prioritising target non-pharmacological interventions for research in Parkinson’s disease: achieving consensus from key stakeholders
title_short Prioritising target non-pharmacological interventions for research in Parkinson’s disease: achieving consensus from key stakeholders
title_full Prioritising target non-pharmacological interventions for research in Parkinson’s disease: achieving consensus from key stakeholders
title_fullStr Prioritising target non-pharmacological interventions for research in Parkinson’s disease: achieving consensus from key stakeholders
title_full_unstemmed Prioritising target non-pharmacological interventions for research in Parkinson’s disease: achieving consensus from key stakeholders
title_sort prioritising target non-pharmacological interventions for research in parkinson’s disease: achieving consensus from key stakeholders
publisher BMC
series Research Involvement and Engagement
issn 2056-7529
publishDate 2020-06-01
description Abstract Background In 2014 Parkinson’s UK conducted a research prioritisation exercise with stakeholders highlighting important clinical research questions. The exercise highlighted the need for effective interventions to be developed and tested to tackle a range of non-motor symptoms including: sleep quality, stress and anxiety, mild cognitive impairment, dementia and urinary problems. The present work set out to build on this exercise by prioritising types of non-pharmacological interventions to be tested to treat the identified non-motor symptoms. Methods A Patient and Public Involvement exercise was used to reach consensus on intervention priorities for the treatment of non-motor symptoms. A Delphi structure was used to support the feedback collected. A first-round prioritisation survey was conducted followed by a panel discussion. Nineteen panellists completed the first-round survey (9 people with Parkinson’s and 10 professionals working in Parkinson’s) and 16 participated in the panel discussion (8 people with Parkinson’s and 8 professionals working in Parkinson’s). A second-round prioritization survey was conducted after the panel discussion with 13 people with Parkinson’s. Results Physical activity, third wave cognitive therapies and cognitive training were rated as priority interventions for the treatment of a range of non-motor symptoms. There was broad agreement on intervention priorities between health care professionals and people with Parkinson’s. A consensus was reached that research should focus on therapies which could be used to treat several different non-motor symptoms. In the context of increasing digitisation, the need for human interaction as an intervention component was highlighted. Conclusion Bringing together Parkinson’s professionals and people with Parkinson’s resulted in a final treatment priority list which should be both feasible to carry out in routine clinical practice and acceptable to both professionals and people with Parkinson’s. The workshop further specified research priorities in Parkinson’s disease based on the current evidence base, stakeholder preferences, and feasibility. Research should focus on developing and testing non-pharmacological treatments which could be effective across a range of symptoms but specifically focusing on tailored physical activity interventions, cognitive therapies and cognitive training.
topic Parkinson’s disease
Research prioritisation
Public and patient involvement
Research engagement
Intervention development
Self-management
url http://link.springer.com/article/10.1186/s40900-020-00212-7
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