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Patient Experience in Early-Stage Parkinson’s Disease: Using a Mixed Methods Analysis to Identify Which Concepts Are Cardinal for Clinical Trial Outcome Assessment
INTRODUCTION: Qualitative research on patient experiences in early-stage Parkinson’s disease (PD) is limited. It is increasingly acknowledged that clinical outcome assessments used in trials do not fully capture the range of symptoms/impacts that are meaningful to people with early-stage PD. We aime...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Healthcare
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9338202/ https://www.ncbi.nlm.nih.gov/pubmed/35778541 http://dx.doi.org/10.1007/s40120-022-00375-3 |
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author | Morel, Thomas Cleanthous, Sophie Andrejack, John Barker, Roger A. Blavat, Geraldine Brooks, William Burns, Paul Cano, Stefan Gallagher, Casey Gosden, Lesley Siu, Carroll Slagle, Ashley F. Trenam, Kate Boroojerdi, Babak Ratcliffe, Natasha Schroeder, Karlin |
author_facet | Morel, Thomas Cleanthous, Sophie Andrejack, John Barker, Roger A. Blavat, Geraldine Brooks, William Burns, Paul Cano, Stefan Gallagher, Casey Gosden, Lesley Siu, Carroll Slagle, Ashley F. Trenam, Kate Boroojerdi, Babak Ratcliffe, Natasha Schroeder, Karlin |
author_sort | Morel, Thomas |
collection | PubMed |
description | INTRODUCTION: Qualitative research on patient experiences in early-stage Parkinson’s disease (PD) is limited. It is increasingly acknowledged that clinical outcome assessments used in trials do not fully capture the range of symptoms/impacts that are meaningful to people with early-stage PD. We aimed to conceptualize the patient experience in early-stage PD and identify, from the patient perspective, those cardinal symptoms/impacts which might be more useful to measure in clinical trials. METHODS: In a mixed-methods analysis, 50 people with early-stage PD and nine relatives were interviewed. Study design and results interpretation were led by a multidisciplinary group of patient, clinical, regulatory, and outcome measurements experts, and patient organization representatives. Identification of the cardinal concepts was informed by the relative frequency of reported concepts combined with insights from patient experts and movement disorder specialists. RESULTS: A conceptual model of the patient experience of early-stage PD was developed. Concept elicitation generated 145 unique concepts mapped across motor and non-motor symptoms, function, and impacts. Bradykinesia/slowness (notably in the form of “functional slowness”), tremor, rigidity/stiffness, mobility (particularly fine motor dexterity and subtle gait abnormalities), fatigue, depression, sleep/dreams, and pain were identified as cardinal in early-stage PD. “Functional slowness” (related to discrete tasks involving the upper limbs, complex mobility tasks, and general activities) was deemed to be more relevant than “difficulty” to patients with early-stage PD, who report being slower at completing tasks rather than encountering significant impairment with task completion. CONCLUSION: Patient experiences in early-stage PD are complex and wide-ranging, and the currently available patient-reported outcome (PRO) instruments do not evaluate many early-stage PD concepts such as functional slowness, fine motor skills, and subtle gait abnormalities. The development of a new PRO instrument, created in conjunction with people with PD, that fully assesses symptoms and the experience of living with early-stage PD, is required. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40120-022-00375-3. |
format | Online Article Text |
id | pubmed-9338202 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Healthcare |
record_format | MEDLINE/PubMed |
spelling | pubmed-93382022022-07-31 Patient Experience in Early-Stage Parkinson’s Disease: Using a Mixed Methods Analysis to Identify Which Concepts Are Cardinal for Clinical Trial Outcome Assessment Morel, Thomas Cleanthous, Sophie Andrejack, John Barker, Roger A. Blavat, Geraldine Brooks, William Burns, Paul Cano, Stefan Gallagher, Casey Gosden, Lesley Siu, Carroll Slagle, Ashley F. Trenam, Kate Boroojerdi, Babak Ratcliffe, Natasha Schroeder, Karlin Neurol Ther Original Research INTRODUCTION: Qualitative research on patient experiences in early-stage Parkinson’s disease (PD) is limited. It is increasingly acknowledged that clinical outcome assessments used in trials do not fully capture the range of symptoms/impacts that are meaningful to people with early-stage PD. We aimed to conceptualize the patient experience in early-stage PD and identify, from the patient perspective, those cardinal symptoms/impacts which might be more useful to measure in clinical trials. METHODS: In a mixed-methods analysis, 50 people with early-stage PD and nine relatives were interviewed. Study design and results interpretation were led by a multidisciplinary group of patient, clinical, regulatory, and outcome measurements experts, and patient organization representatives. Identification of the cardinal concepts was informed by the relative frequency of reported concepts combined with insights from patient experts and movement disorder specialists. RESULTS: A conceptual model of the patient experience of early-stage PD was developed. Concept elicitation generated 145 unique concepts mapped across motor and non-motor symptoms, function, and impacts. Bradykinesia/slowness (notably in the form of “functional slowness”), tremor, rigidity/stiffness, mobility (particularly fine motor dexterity and subtle gait abnormalities), fatigue, depression, sleep/dreams, and pain were identified as cardinal in early-stage PD. “Functional slowness” (related to discrete tasks involving the upper limbs, complex mobility tasks, and general activities) was deemed to be more relevant than “difficulty” to patients with early-stage PD, who report being slower at completing tasks rather than encountering significant impairment with task completion. CONCLUSION: Patient experiences in early-stage PD are complex and wide-ranging, and the currently available patient-reported outcome (PRO) instruments do not evaluate many early-stage PD concepts such as functional slowness, fine motor skills, and subtle gait abnormalities. The development of a new PRO instrument, created in conjunction with people with PD, that fully assesses symptoms and the experience of living with early-stage PD, is required. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40120-022-00375-3. Springer Healthcare 2022-07-01 /pmc/articles/PMC9338202/ /pubmed/35778541 http://dx.doi.org/10.1007/s40120-022-00375-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial 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-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Original Research Morel, Thomas Cleanthous, Sophie Andrejack, John Barker, Roger A. Blavat, Geraldine Brooks, William Burns, Paul Cano, Stefan Gallagher, Casey Gosden, Lesley Siu, Carroll Slagle, Ashley F. Trenam, Kate Boroojerdi, Babak Ratcliffe, Natasha Schroeder, Karlin Patient Experience in Early-Stage Parkinson’s Disease: Using a Mixed Methods Analysis to Identify Which Concepts Are Cardinal for Clinical Trial Outcome Assessment |
title | Patient Experience in Early-Stage Parkinson’s Disease: Using a Mixed Methods Analysis to Identify Which Concepts Are Cardinal for Clinical Trial Outcome Assessment |
title_full | Patient Experience in Early-Stage Parkinson’s Disease: Using a Mixed Methods Analysis to Identify Which Concepts Are Cardinal for Clinical Trial Outcome Assessment |
title_fullStr | Patient Experience in Early-Stage Parkinson’s Disease: Using a Mixed Methods Analysis to Identify Which Concepts Are Cardinal for Clinical Trial Outcome Assessment |
title_full_unstemmed | Patient Experience in Early-Stage Parkinson’s Disease: Using a Mixed Methods Analysis to Identify Which Concepts Are Cardinal for Clinical Trial Outcome Assessment |
title_short | Patient Experience in Early-Stage Parkinson’s Disease: Using a Mixed Methods Analysis to Identify Which Concepts Are Cardinal for Clinical Trial Outcome Assessment |
title_sort | patient experience in early-stage parkinson’s disease: using a mixed methods analysis to identify which concepts are cardinal for clinical trial outcome assessment |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9338202/ https://www.ncbi.nlm.nih.gov/pubmed/35778541 http://dx.doi.org/10.1007/s40120-022-00375-3 |
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