Cocreating the Visualization of Digital Mobility Outcomes: Delphi-Type Process With Patients

Recent technological advances in wearable devices offer new potential for measuring mobility in real-world contexts. Mobilise-D has validated digital mobility outcomes to provide novel outcomes and end points in clinical research of 4 different long-term health conditions (Parkinson disease, multipl...

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Published inJMIR formative research Vol. 9; p. e68782
Main Authors Lumsdon, Jack, Wilson, Cameron, Alcock, Lisa, Becker, Clemens, Benvenuti, Francesco, Bonci, Tecla, van den Brande, Koen, Brittain, Gavin, Brown, Philip, Buckley, Ellen, Caruso, Marco, Caulfield, Brian, Cereatti, Andrea, Delgado-Ortiz, Laura, Del Din, Silvia, Evers, Jordi, Garcia-Aymerich, Judith, Gaßner, Heiko, Gur Arieh, Tova, Hansen, Clint, Hausdorff, Jeffrey M, Hiden, Hugo, Hume, Emily, Kirk, Cameron, Maetzler, Walter, Megaritis, Dimitrios, Rochester, Lynn, Scott, Kirsty, Sharrack, Basil, Sutton, Norman, Vereijken, Beatrix, Vogiatzis, Ioannis, Yarnall, Alison, Keogh, Alison, Cantu, Alma
Format Journal Article
LanguageEnglish
Published Canada JMIR Publications 09.05.2025
Subjects
Online AccessGet full text
ISSN2561-326X
2561-326X
DOI10.2196/68782

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Abstract Recent technological advances in wearable devices offer new potential for measuring mobility in real-world contexts. Mobilise-D has validated digital mobility outcomes to provide novel outcomes and end points in clinical research of 4 different long-term health conditions (Parkinson disease, multiple sclerosis, chronic obstructive pulmonary disease, and proximal femoral fracture). These outcomes also provide unique information that is important to patients; however, there is limited literature that explores the optimal methods to achieve this, such as the best way to visualize patients' data. This study aimed to identify meaningful outcomes for each condition and how to best visualize them from the perspective of end users. Using a Delphi-type protocol with patients as subject matter experts, we gathered iterative feedback on the cocreation of visualizations through 3 rounds of questionnaires. An open-ended questionnaire was used in round 1 to understand what aspects of mobility were most influenced by their health condition. These responses were mapped onto relevant digital mobility outcomes and walking experiences and then prioritized for visualization. Using patient responses, we worked alongside researchers, clinicians, and a patient advisory group to develop visualizations that depicted a week of mobility data. During rounds 2 and 3, participants rated usefulness and ease of understanding on a 5-point Likert scale and provided unstructured feedback in comment boxes for each visualization. Visualizations were refined using the feedback from round 2 before receiving further feedback in round 3. Participation varied across rounds 1 to 3 (n=48, n=79, and n=78, respectively). Round 1 identified important outcomes and contexts for each health condition, such as walking speed and stride length for people with Parkinson disease or multiple sclerosis and number of steps for people with chronic obstructive pulmonary disease or proximal femoral fracture. The consensus was not reached for any visualization reviewed in round 2 or 3. Feedback was generally positive, and some participants reported that they were able to understand the visualization and interpret what the visualization represented. Through the feedback provided and existing data visualization principles, we developed recommendations for future visualizations of mobility- and health-related data. Visualizations should be readable by ensuring that large and clear fonts are used and should be friendly for people with vision impairments, such as color blindness. Patients have a strong understanding of their own condition and its variability; hence, adding additional factors into visualizations is recommended to better reflect the nuances of a condition. Ensuring that outcomes and visualizations are meaningful requires close collaboration with patients throughout the development process.
AbstractList BackgroundRecent technological advances in wearable devices offer new potential for measuring mobility in real-world contexts. Mobilise-D has validated digital mobility outcomes to provide novel outcomes and end points in clinical research of 4 different long-term health conditions (Parkinson disease, multiple sclerosis, chronic obstructive pulmonary disease, and proximal femoral fracture). These outcomes also provide unique information that is important to patients; however, there is limited literature that explores the optimal methods to achieve this, such as the best way to visualize patients’ data. ObjectiveThis study aimed to identify meaningful outcomes for each condition and how to best visualize them from the perspective of end users. MethodsUsing a Delphi-type protocol with patients as subject matter experts, we gathered iterative feedback on the cocreation of visualizations through 3 rounds of questionnaires. An open-ended questionnaire was used in round 1 to understand what aspects of mobility were most influenced by their health condition. These responses were mapped onto relevant digital mobility outcomes and walking experiences and then prioritized for visualization. Using patient responses, we worked alongside researchers, clinicians, and a patient advisory group to develop visualizations that depicted a week of mobility data. During rounds 2 and 3, participants rated usefulness and ease of understanding on a 5-point Likert scale and provided unstructured feedback in comment boxes for each visualization. Visualizations were refined using the feedback from round 2 before receiving further feedback in round 3. ResultsParticipation varied across rounds 1 to 3 (n=48, n=79, and n=78, respectively). Round 1 identified important outcomes and contexts for each health condition, such as walking speed and stride length for people with Parkinson disease or multiple sclerosis and number of steps for people with chronic obstructive pulmonary disease or proximal femoral fracture. The consensus was not reached for any visualization reviewed in round 2 or 3. Feedback was generally positive, and some participants reported that they were able to understand the visualization and interpret what the visualization represented. ConclusionsThrough the feedback provided and existing data visualization principles, we developed recommendations for future visualizations of mobility- and health-related data. Visualizations should be readable by ensuring that large and clear fonts are used and should be friendly for people with vision impairments, such as color blindness. Patients have a strong understanding of their own condition and its variability; hence, adding additional factors into visualizations is recommended to better reflect the nuances of a condition. Ensuring that outcomes and visualizations are meaningful requires close collaboration with patients throughout the development process.
Recent technological advances in wearable devices offer new potential for measuring mobility in real-world contexts. Mobilise-D has validated digital mobility outcomes to provide novel outcomes and end points in clinical research of 4 different long-term health conditions (Parkinson disease, multiple sclerosis, chronic obstructive pulmonary disease, and proximal femoral fracture). These outcomes also provide unique information that is important to patients; however, there is limited literature that explores the optimal methods to achieve this, such as the best way to visualize patients' data.BACKGROUNDRecent technological advances in wearable devices offer new potential for measuring mobility in real-world contexts. Mobilise-D has validated digital mobility outcomes to provide novel outcomes and end points in clinical research of 4 different long-term health conditions (Parkinson disease, multiple sclerosis, chronic obstructive pulmonary disease, and proximal femoral fracture). These outcomes also provide unique information that is important to patients; however, there is limited literature that explores the optimal methods to achieve this, such as the best way to visualize patients' data.This study aimed to identify meaningful outcomes for each condition and how to best visualize them from the perspective of end users.OBJECTIVEThis study aimed to identify meaningful outcomes for each condition and how to best visualize them from the perspective of end users.Using a Delphi-type protocol with patients as subject matter experts, we gathered iterative feedback on the cocreation of visualizations through 3 rounds of questionnaires. An open-ended questionnaire was used in round 1 to understand what aspects of mobility were most influenced by their health condition. These responses were mapped onto relevant digital mobility outcomes and walking experiences and then prioritized for visualization. Using patient responses, we worked alongside researchers, clinicians, and a patient advisory group to develop visualizations that depicted a week of mobility data. During rounds 2 and 3, participants rated usefulness and ease of understanding on a 5-point Likert scale and provided unstructured feedback in comment boxes for each visualization. Visualizations were refined using the feedback from round 2 before receiving further feedback in round 3.METHODSUsing a Delphi-type protocol with patients as subject matter experts, we gathered iterative feedback on the cocreation of visualizations through 3 rounds of questionnaires. An open-ended questionnaire was used in round 1 to understand what aspects of mobility were most influenced by their health condition. These responses were mapped onto relevant digital mobility outcomes and walking experiences and then prioritized for visualization. Using patient responses, we worked alongside researchers, clinicians, and a patient advisory group to develop visualizations that depicted a week of mobility data. During rounds 2 and 3, participants rated usefulness and ease of understanding on a 5-point Likert scale and provided unstructured feedback in comment boxes for each visualization. Visualizations were refined using the feedback from round 2 before receiving further feedback in round 3.Participation varied across rounds 1 to 3 (n=48, n=79, and n=78, respectively). Round 1 identified important outcomes and contexts for each health condition, such as walking speed and stride length for people with Parkinson disease or multiple sclerosis and number of steps for people with chronic obstructive pulmonary disease or proximal femoral fracture. The consensus was not reached for any visualization reviewed in round 2 or 3. Feedback was generally positive, and some participants reported that they were able to understand the visualization and interpret what the visualization represented.RESULTSParticipation varied across rounds 1 to 3 (n=48, n=79, and n=78, respectively). Round 1 identified important outcomes and contexts for each health condition, such as walking speed and stride length for people with Parkinson disease or multiple sclerosis and number of steps for people with chronic obstructive pulmonary disease or proximal femoral fracture. The consensus was not reached for any visualization reviewed in round 2 or 3. Feedback was generally positive, and some participants reported that they were able to understand the visualization and interpret what the visualization represented.Through the feedback provided and existing data visualization principles, we developed recommendations for future visualizations of mobility- and health-related data. Visualizations should be readable by ensuring that large and clear fonts are used and should be friendly for people with vision impairments, such as color blindness. Patients have a strong understanding of their own condition and its variability; hence, adding additional factors into visualizations is recommended to better reflect the nuances of a condition. Ensuring that outcomes and visualizations are meaningful requires close collaboration with patients throughout the development process.CONCLUSIONSThrough the feedback provided and existing data visualization principles, we developed recommendations for future visualizations of mobility- and health-related data. Visualizations should be readable by ensuring that large and clear fonts are used and should be friendly for people with vision impairments, such as color blindness. Patients have a strong understanding of their own condition and its variability; hence, adding additional factors into visualizations is recommended to better reflect the nuances of a condition. Ensuring that outcomes and visualizations are meaningful requires close collaboration with patients throughout the development process.
Background:Recent technological advances in wearable devices offer new potential for measuring mobility in real-world contexts. Mobilise-D has validated digital mobility outcomes to provide novel outcomes and end points in clinical research of 4 different long-term health conditions (Parkinson disease, multiple sclerosis, chronic obstructive pulmonary disease, and proximal femoral fracture). These outcomes also provide unique information that is important to patients; however, there is limited literature that explores the optimal methods to achieve this, such as the best way to visualize patients’ data.Objective:This study aimed to identify meaningful outcomes for each condition and how to best visualize them from the perspective of end users.Methods:Using a Delphi-type protocol with patients as subject matter experts, we gathered iterative feedback on the cocreation of visualizations through 3 rounds of questionnaires. An open-ended questionnaire was used in round 1 to understand what aspects of mobility were most influenced by their health condition. These responses were mapped onto relevant digital mobility outcomes and walking experiences and then prioritized for visualization. Using patient responses, we worked alongside researchers, clinicians, and a patient advisory group to develop visualizations that depicted a week of mobility data. During rounds 2 and 3, participants rated usefulness and ease of understanding on a 5-point Likert scale and provided unstructured feedback in comment boxes for each visualization. Visualizations were refined using the feedback from round 2 before receiving further feedback in round 3.Results:Participation varied across rounds 1 to 3 (n=48, n=79, and n=78, respectively). Round 1 identified important outcomes and contexts for each health condition, such as walking speed and stride length for people with Parkinson disease or multiple sclerosis and number of steps for people with chronic obstructive pulmonary disease or proximal femoral fracture. The consensus was not reached for any visualization reviewed in round 2 or 3. Feedback was generally positive, and some participants reported that they were able to understand the visualization and interpret what the visualization represented.Conclusions:Through the feedback provided and existing data visualization principles, we developed recommendations for future visualizations of mobility- and health-related data. Visualizations should be readable by ensuring that large and clear fonts are used and should be friendly for people with vision impairments, such as color blindness. Patients have a strong understanding of their own condition and its variability; hence, adding additional factors into visualizations is recommended to better reflect the nuances of a condition. Ensuring that outcomes and visualizations are meaningful requires close collaboration with patients throughout the development process.
Recent technological advances in wearable devices offer new potential for measuring mobility in real-world contexts. Mobilise-D has validated digital mobility outcomes to provide novel outcomes and end points in clinical research of 4 different long-term health conditions (Parkinson disease, multiple sclerosis, chronic obstructive pulmonary disease, and proximal femoral fracture). These outcomes also provide unique information that is important to patients; however, there is limited literature that explores the optimal methods to achieve this, such as the best way to visualize patients' data. This study aimed to identify meaningful outcomes for each condition and how to best visualize them from the perspective of end users. Using a Delphi-type protocol with patients as subject matter experts, we gathered iterative feedback on the cocreation of visualizations through 3 rounds of questionnaires. An open-ended questionnaire was used in round 1 to understand what aspects of mobility were most influenced by their health condition. These responses were mapped onto relevant digital mobility outcomes and walking experiences and then prioritized for visualization. Using patient responses, we worked alongside researchers, clinicians, and a patient advisory group to develop visualizations that depicted a week of mobility data. During rounds 2 and 3, participants rated usefulness and ease of understanding on a 5-point Likert scale and provided unstructured feedback in comment boxes for each visualization. Visualizations were refined using the feedback from round 2 before receiving further feedback in round 3. Participation varied across rounds 1 to 3 (n=48, n=79, and n=78, respectively). Round 1 identified important outcomes and contexts for each health condition, such as walking speed and stride length for people with Parkinson disease or multiple sclerosis and number of steps for people with chronic obstructive pulmonary disease or proximal femoral fracture. The consensus was not reached for any visualization reviewed in round 2 or 3. Feedback was generally positive, and some participants reported that they were able to understand the visualization and interpret what the visualization represented. Through the feedback provided and existing data visualization principles, we developed recommendations for future visualizations of mobility- and health-related data. Visualizations should be readable by ensuring that large and clear fonts are used and should be friendly for people with vision impairments, such as color blindness. Patients have a strong understanding of their own condition and its variability; hence, adding additional factors into visualizations is recommended to better reflect the nuances of a condition. Ensuring that outcomes and visualizations are meaningful requires close collaboration with patients throughout the development process.
Author Caruso, Marco
Gaßner, Heiko
Becker, Clemens
Alcock, Lisa
Cantu, Alma
Sutton, Norman
Yarnall, Alison
Rochester, Lynn
Caulfield, Brian
Hansen, Clint
Kirk, Cameron
Buckley, Ellen
Wilson, Cameron
Keogh, Alison
Hume, Emily
Benvenuti, Francesco
Vereijken, Beatrix
Bonci, Tecla
Maetzler, Walter
Megaritis, Dimitrios
Del Din, Silvia
Gur Arieh, Tova
Scott, Kirsty
Vogiatzis, Ioannis
Cereatti, Andrea
Garcia-Aymerich, Judith
Brown, Philip
Evers, Jordi
Delgado-Ortiz, Laura
Hausdorff, Jeffrey M
Lumsdon, Jack
van den Brande, Koen
Brittain, Gavin
Sharrack, Basil
Hiden, Hugo
AuthorAffiliation 19 Network in Epidemiology and Public Health Center for Biomedical Research Madrid Spain
30 School of Medicine Trinity College Dublin Dublin Ireland
27 School of Computer Science Newcastle University Newcastle Upon Tyne United Kingdom
9 Insigneo Institute for Silico Medicine University of Sheffield Sheffield United Kingdom
1 Population Health Sciences Institute Faculty of Medical Sciences Newcastle University Newcastle Upon Tyne United Kingdom
18 Department of Medicine and Life Sciences Pompeu Fabra University Barcelona Spain
14 Department of Electronics and Telecommunications Politecnico di Torino Turin Italy
4 NIHR Newcastle Biomedical Research Centre Newcastle University and The Newcastle Upon Tyne Hospitals NHS Foundation Trust Newcastle upon Tyne United Kingdom
3 Translational and Clinical Research Institute Faculty of Medical Sciences Newcastle University Newcastle Upon Tyne United Kingdom
13 Division of Clinical Medicine University of Sheffield Sheffield United Kingdom
21 Department of Mo
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– name: 25 Rush Alzheimer’s Disease Center and Department of Orthopaedic Surgery Rush University Medical Center Chicago, IL United States
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– name: 9 Insigneo Institute for Silico Medicine University of Sheffield Sheffield United Kingdom
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– name: 22 Fraunhofer Institute for Integrated Circuits IIS Erlangen Germany
– name: 28 Department of Sport, Exercise and Rehabilitation Northumbria University Newcastle Upon Tyne United Kingdom
– name: 21 Department of Molecular Neurology University Hospital Erlangen Erlangen Germany
– name: 8 School of Mechanical, Aerospace and Civil Engineering University of Sheffield Sheffield United Kingdom
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– name: 20 McRoberts BV The Hague The Netherlands
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/40344668$$D View this record in MEDLINE/PubMed
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ContentType Journal Article
Copyright Jack Lumsdon, Cameron Wilson, Lisa Alcock, Clemens Becker, Francesco Benvenuti, Tecla Bonci, Koen van den Brande, Gavin Brittain, Philip Brown, Ellen Buckley, Marco Caruso, Brian Caulfield, Andrea Cereatti, Laura Delgado-Ortiz, Silvia Del Din, Jordi Evers, Judith Garcia-Aymerich, Heiko Gaßner, Tova Gur Arieh, Clint Hansen, Jeffrey M Hausdorff, Hugo Hiden, Emily Hume, Cameron Kirk, Walter Maetzler, Dimitrios Megaritis, Lynn Rochester, Kirsty Scott, Basil Sharrack, Norman Sutton, Beatrix Vereijken, Ioannis Vogiatzis, Alison Yarnall, Alison Keogh, Alma Cantu. Originally published in JMIR Formative Research (https://formative.jmir.org), 09.05.2025.
2025. This work is licensed under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Jack Lumsdon, Cameron Wilson, Lisa Alcock, Clemens Becker, Francesco Benvenuti, Tecla Bonci, Koen van den Brande, Gavin Brittain, Philip Brown, Ellen Buckley, Marco Caruso, Brian Caulfield, Andrea Cereatti, Laura Delgado-Ortiz, Silvia Del Din, Jordi Evers, Judith Garcia-Aymerich, Heiko Gaßner, Tova Gur Arieh, Clint Hansen, Jeffrey M Hausdorff, Hugo Hiden, Emily Hume, Cameron Kirk, Walter Maetzler, Dimitrios Megaritis, Lynn Rochester, Kirsty Scott, Basil Sharrack, Norman Sutton, Beatrix Vereijken, Ioannis Vogiatzis, Alison Yarnall, Alison Keogh, Alma Cantu. Originally published in JMIR Formative Research (https://formative.jmir.org), 09.05.2025. 2025
Copyright_xml – notice: Jack Lumsdon, Cameron Wilson, Lisa Alcock, Clemens Becker, Francesco Benvenuti, Tecla Bonci, Koen van den Brande, Gavin Brittain, Philip Brown, Ellen Buckley, Marco Caruso, Brian Caulfield, Andrea Cereatti, Laura Delgado-Ortiz, Silvia Del Din, Jordi Evers, Judith Garcia-Aymerich, Heiko Gaßner, Tova Gur Arieh, Clint Hansen, Jeffrey M Hausdorff, Hugo Hiden, Emily Hume, Cameron Kirk, Walter Maetzler, Dimitrios Megaritis, Lynn Rochester, Kirsty Scott, Basil Sharrack, Norman Sutton, Beatrix Vereijken, Ioannis Vogiatzis, Alison Yarnall, Alison Keogh, Alma Cantu. Originally published in JMIR Formative Research (https://formative.jmir.org), 09.05.2025.
– notice: 2025. This work is licensed under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
– notice: Jack Lumsdon, Cameron Wilson, Lisa Alcock, Clemens Becker, Francesco Benvenuti, Tecla Bonci, Koen van den Brande, Gavin Brittain, Philip Brown, Ellen Buckley, Marco Caruso, Brian Caulfield, Andrea Cereatti, Laura Delgado-Ortiz, Silvia Del Din, Jordi Evers, Judith Garcia-Aymerich, Heiko Gaßner, Tova Gur Arieh, Clint Hansen, Jeffrey M Hausdorff, Hugo Hiden, Emily Hume, Cameron Kirk, Walter Maetzler, Dimitrios Megaritis, Lynn Rochester, Kirsty Scott, Basil Sharrack, Norman Sutton, Beatrix Vereijken, Ioannis Vogiatzis, Alison Yarnall, Alison Keogh, Alma Cantu. Originally published in JMIR Formative Research (https://formative.jmir.org), 09.05.2025. 2025
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License Jack Lumsdon, Cameron Wilson, Lisa Alcock, Clemens Becker, Francesco Benvenuti, Tecla Bonci, Koen van den Brande, Gavin Brittain, Philip Brown, Ellen Buckley, Marco Caruso, Brian Caulfield, Andrea Cereatti, Laura Delgado-Ortiz, Silvia Del Din, Jordi Evers, Judith Garcia-Aymerich, Heiko Gaßner, Tova Gur Arieh, Clint Hansen, Jeffrey M Hausdorff, Hugo Hiden, Emily Hume, Cameron Kirk, Walter Maetzler, Dimitrios Megaritis, Lynn Rochester, Kirsty Scott, Basil Sharrack, Norman Sutton, Beatrix Vereijken, Ioannis Vogiatzis, Alison Yarnall, Alison Keogh, Alma Cantu. Originally published in JMIR Formative Research (https://formative.jmir.org), 09.05.2025.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in JMIR Formative Research, is properly cited. The complete bibliographic information, a link to the original publication on https://formative.jmir.org, as well as this copyright and license information must be included.
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Snippet Recent technological advances in wearable devices offer new potential for measuring mobility in real-world contexts. Mobilise-D has validated digital mobility...
Background:Recent technological advances in wearable devices offer new potential for measuring mobility in real-world contexts. Mobilise-D has validated...
BackgroundRecent technological advances in wearable devices offer new potential for measuring mobility in real-world contexts. Mobilise-D has validated digital...
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SubjectTerms Adult
Aged
Chronic obstructive pulmonary disease
Collaboration
Data visualization
Delphi method
Delphi Technique
Feedback
Female
Fractures
Hip joint
Humans
Male
Middle Aged
Multiple Sclerosis - physiopathology
Original Paper
Parkinson Disease - physiopathology
Parkinson's disease
Patients
Pulmonary Disease, Chronic Obstructive - physiopathology
Questionnaires
Surveys and Questionnaires
Visualization
Walking - physiology
Wearable computers
Wearable Electronic Devices
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Title Cocreating the Visualization of Digital Mobility Outcomes: Delphi-Type Process With Patients
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