Waters-Harvey, B. orcid.org/0000-0002-1216-0867, Kane, K. orcid.org/0000-0002-2714-8035, Griffiths, A.W. orcid.org/0000-0001-9388-9168 et al. (15 more authors) (2026) Co-designing a care coordination intervention for people with motor neuron disease: protocol for a mixed methods study. JMIR Research Protocols, 15. e96327. ISSN: 1929-0748
Abstract
Background:
Motor neuron disease (MND), also known as amyotrophic lateral sclerosis (ALS), is a rapidly progressive neurological condition that requires complex multidisciplinary care. Within the United Kingdom, specialist centers provide expert interventions, while day-to-day support often relies on local nonspecialist community health and social care professionals. This is due to the distance between people’s homes and specialist centers, as well as the availability of specialist health and social care professionals. This can lead to fragmented communication and emotional, physical, and financial burdens, and it can be time-consuming for people living with MND, their carers, and the health care professionals involved in their care. Despite the recognized need for better care coordination, it remains inadequate in practice, with a current lack of specific evidence-based interventions for achieving this.
Objective:
The MND Together project aims to address these systemic gaps by (1) developing a national picture of care coordination in England and Wales, (2) identifying barriers and facilitators to coordination within specialist and nonspecialist settings, and (3) co-designing a practical care coordination tool with key stakeholders.
Methods:
This protocol outlines the co-design of an intervention underpinned by the Behavior Change Wheel and the Socioecological Model. First, a mixed methods, multicenter study will be conducted to develop a national picture, comprising focus groups with people living with MND, carers, and health and social care professionals. Second, focused ethnography will be conducted in 5 MND specialist centers and their catchment areas, involving 25 people living with MND, to explore the barriers and facilitators to coordination in practice. Finally, a series of co-design workshops will be conducted to identify key priorities for care coordination and to develop a new intervention, the MND Together tool.
Results:
The project started in September 2025 and will run until October 2027. Workstream 1 started in December 2025, with recruitment beginning at the first site in February 2026. To date, we have recruited 23 people living with MND and carers as well as 16 health and social care professionals across 4 of the 9 sites. Workstream 1 will end in August 2026, with results published at the end of 2026. Workstream 2 began in May 2026 and will run until February 2027, with results published in the summer of 2027. Workstream 3 will begin in March 2027 and conclude with the co-design intervention developed by late 2027. This will then be piloted in practice.
Conclusions:
By combining several methodologies with meaningful patient and public involvement and engagement, MND Together seeks to bridge the gap between specialist and community-based services. The MND Together tool aims to improve the quality of care and ensure that expert MND support is accessible as close as possible to every patient’s home.
International Registered Report Identifier (IRRID): DERR1-10.2196/96327
Metadata
| Item Type: | Article |
|---|---|
| Authors/Creators: |
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| Copyright, Publisher and Additional Information: | © Bryony Waters-Harvey, Kathleen Kane, Alys Wyn Griffiths, Grahame Smith, Clare M Bartlett, Lise Sproson, Sandra Smith, Jennie Starkey, Amy Clift, Theocharis Stavroulakis, Esther Hobson, Emily Mayberry, Alicia O'Cathain, Caroline Bidder, Katherine Kennedy, Jane Gibson, Christopher McDermott, Liam Knox. Originally published in JMIR Research Protocols (https://www.researchprotocols.org), 4.Aug.2026. 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 Research Protocols, is properly cited. The complete bibliographic information, a link to the original publication on https://www.researchprotocols.org, as well as this copyright and license information must be included. |
| Keywords: | ALS; MND; amyotrophic lateral sclerosis; care coordination; co-design; health care; motor neuron disease; qualitative methods; Humans; Motor Neuron Disease; Amyotrophic Lateral Sclerosis; England; United Kingdom; Wales |
| Dates: |
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| Institution: | The University of Sheffield |
| Academic Units: | The University of Sheffield > Faculty of Medicine, Dentistry and Health (Sheffield) > School of Medicine and Population Health The University of Sheffield > Faculty of Medicine, Dentistry and Health (Sheffield) > Department of Neuroscience (Sheffield) |
| Funding Information: | Funder Grant number DEPARTMENT OF HEALTH AND SOCIAL CARE / DHSC NIHR304149 DEPARTMENT OF HEALTH AND SOCIAL CARE NIHR166956 |
| Date Deposited: | 20 Aug 2026 10:13 |
| Last Modified: | 20 Aug 2026 10:13 |
| Status: | Published |
| Publisher: | JMIR Publications Inc. |
| Refereed: | Yes |
| Identification Number: | 10.2196/96327 |
| Related URLs: | |
| Sustainable Development Goals: | |
| Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:244525 |
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Filename: resprot-2026-1-e96327.pdf
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