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      Compound impact of cognitive and physical decline: A qualitative interview study of people with Parkinson's and cognitive impairment, caregivers and professionals

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          Abstract

          Background

          Cognitive impairment is common in Parkinson's disease and is associated with poorer quality of life and increased caregiver distress, but little qualitative information is available on lived experiences of people with Parkinson's who also have cognitive impairment.

          Objectives

          The aim of this study was to explore the challenges of cognitive impairment in Parkinson's, triangulating the perspectives of people with Parkinson's, caregivers and healthcare professionals.

          Methods

          Semistructured interviews were conducted with 11 people with Parkinson's and cognitive impairment, 10 family caregivers and 27 healthcare professionals, using purposive sampling in the United Kingdom (2019–2021). Cognitive impairment was identified by healthcare professionals and required subjective symptoms. Relevant cognitive diagnoses were recorded. Interviews were audio‐recorded, transcribed and analysed using reflexive thematic analysis.

          Results

          An overarching concept of the compound impact of cognitive and physical decline was developed, with six themes. Four themes describe the experience of living with cognitive impairment in Parkinson's: (1) Challenges in Daily Activities, (2) Psychological Impact and (3) Evolving Communication Difficulties together contributing to (4) Social Shift, encompassing a reduction in wider social activities but intensification of close relationships with increased dependence. A fifth theme (5) Living Well describes positive influences on these experiences, encompassing intrinsic motivation, self‐management strategies and supportive relationships. Furthermore, underlying and shaping the whole experience was the sixth theme: (6) Preconceptions about Cognitive Impairment, describing fear and denial of symptoms and poor understanding of the nature of cognitive impairment in Parkinson's, with differences to other dementia pathologies.

          Conclusions

          Cognitive impairment superimposed on the existing challenges of Parkinson's has a multifaceted impact and makes living with the condition arduous. Increased understanding of the experiences of this group and employing the identified facilitators for living well may be able to improve patient and caregiver experiences.

          Patient or Public Contribution

          Two people with Parkinson's and cognitive impairment and three caregivers contributed to the study. Between them they contributed throughout the entirety of the project, giving input at conceptualisation as well as advice and review of interview questions, participant information leaflets, recruitment, interpretation of findings and summaries of the project.

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          Most cited references72

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          Standards for reporting qualitative research: a synthesis of recommendations.

          Standards for reporting exist for many types of quantitative research, but currently none exist for the broad spectrum of qualitative research. The purpose of the present study was to formulate and define standards for reporting qualitative research while preserving the requisite flexibility to accommodate various paradigms, approaches, and methods.
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            Sample Size in Qualitative Interview Studies: Guided by Information Power

            Sample sizes must be ascertained in qualitative studies like in quantitative studies but not by the same means. The prevailing concept for sample size in qualitative studies is "saturation." Saturation is closely tied to a specific methodology, and the term is inconsistently applied. We propose the concept "information power" to guide adequate sample size for qualitative studies. Information power indicates that the more information the sample holds, relevant for the actual study, the lower amount of participants is needed. We suggest that the size of a sample with sufficient information power depends on (a) the aim of the study, (b) sample specificity, (c) use of established theory, (d) quality of dialogue, and (e) analysis strategy. We present a model where these elements of information and their relevant dimensions are related to information power. Application of this model in the planning and during data collection of a qualitative study is discussed.
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              One size fits all? What counts as quality practice in (reflexive) thematic analysis?

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                Author and article information

                Contributors
                Role: Clinical Research Fellow
                Role: Associate Professor
                Role: Dementia Nurse Specialist
                Role: Research Co‐ordinator
                Role: Clinical Doctoral Research Fellow
                Role: Professor
                Role: Lecturer
                Role: Professora.schrag@ucl.ac.uk
                Journal
                Health Expect
                Health Expect
                10.1111/(ISSN)1369-7625
                HEX
                Health Expectations : An International Journal of Public Participation in Health Care and Health Policy
                John Wiley and Sons Inc. (Hoboken )
                1369-6513
                1369-7625
                12 January 2024
                February 2024
                : 27
                : 1 ( doiID: 10.1111/hex.v27.1 )
                : e13950
                Affiliations
                [ 1 ] Department of Clinical Neurosciences, Queen Square Institute of Neurology, University College London Royal Free Hospital London UK
                [ 2 ] Research Department of Primary Care and Population Health, Centre for Ageing Population Studies University College London London UK
                Author notes
                [*] [* ] Correspondence Anette Schrag, MD, PhD, Professor, Department of Clinical Neurosciences, Queen Square Institute of Neurology, University College London, Royal Free Hospital, Rowland Hill St, London NW3 2PF, UK.

                Email: a.schrag@ 123456ucl.ac.uk

                Author information
                http://orcid.org/0000-0002-0951-7941
                http://orcid.org/0000-0001-7757-5353
                http://orcid.org/0000-0002-8918-0436
                http://orcid.org/0000-0002-3028-3975
                http://orcid.org/0000-0002-1239-3417
                http://orcid.org/0000-0003-2173-2430
                http://orcid.org/0000-0001-6773-9393
                http://orcid.org/0000-0002-9872-6680
                Article
                HEX13950
                10.1111/hex.13950
                10785559
                80909105-5a4b-4523-b029-84c9d79890d7
                © 2024 The Authors. Health Expectations published by John Wiley & Sons Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 23 November 2023
                : 15 May 2023
                : 14 December 2023
                Page count
                Figures: 1, Tables: 6, Pages: 14, Words: 8981
                Funding
                Funded by: NIHR School of Primary Care Research
                Award ID: SPCR‐2014‐10043
                Funded by: National Institute for Health and Care Research
                Award ID: RP‐PG‐1016‐20001
                Funded by: Rosetrees Trust and Royal College of Physicians , doi 10.13039/501100000395;
                Award ID: RCP‐2020\11
                Categories
                Original Article
                Original Articles
                Custom metadata
                2.0
                February 2024
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.3.6 mode:remove_FC converted:12.01.2024

                Health & Social care
                cognitive impairment,lived experience,parkinson's disease,parkinson's disease dementia,qualitative

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