An online pain management program for people with hypermobile Ehlers-Danlos Syndrome or hypermobility spectrum disorder : A three-staged development process

Journal article


Chew, Min Tze, Ilhan, Emre, Nicholson, Leslie L., Kobayashi, Sarah and Chan, Cliffton. (2025). An online pain management program for people with hypermobile Ehlers-Danlos Syndrome or hypermobility spectrum disorder : A three-staged development process. Disability and Rehabilitation. 47(2), pp. 414-424. https://doi.org/10.1080/09638288.2024.2351180
AuthorsChew, Min Tze, Ilhan, Emre, Nicholson, Leslie L., Kobayashi, Sarah and Chan, Cliffton
Abstract

Purpose
Hypermobile Ehlers-Danlos Syndrome (hEDS) and hypermobility spectrum disorder (HSD) are painful, chronic and multi-systemic conditions. No online pain management programs for hEDS/HSD currently exist. We aimed to develop one by exploring what people with hEDS/HSD want in such programs.

Materials and methods
A Delphi was conducted via online surveys of stakeholders: participants with hEDS/HSD and healthcare professionals (HCP). In survey 1, participants were asked if a hEDS/HSD-specific online pain management program was important, listing up to 20 topics important to know about pain. In survey 2, participants rated the importance of those topics. Consensus was set as ≥75% rating of at least “important”. Using topics that reached consensus, the online program was developed. Usability testing was performed using the Systems Usability Scale (SUS).

Results
396 hEDS/HSD and 29 HCP completed survey 1; 151 hEDS/HSD and 12 HCP completed survey 2. 81% of hEDS/HSD and 69% of HCP rated a hEDS/HSD-specific program as at least “important”. Thirty-five topics reached consensus to guide content for the HOPE program (Hypermobile Online Pain managemEnt). SUS score was 82.5, corresponding to “high acceptability”.

Conclusions
A hEDS/HSD-specific online pain management program is important to stakeholders. Utilising a Delphi approach to incorporate stakeholder input, an evidence-informed and user appropriate program was developed.

IMPLICATIONS FOR REHABILITATION
• Pain is one of the most common and impactful symptom affecting those with Hypermobile Ehlers-Danlos Syndrome (hEDS) and hypermobility spectrum disorder (HSD).

• Online pain management programs are effective in other chronic conditions such as Fibromyalgia and Rheumatoid Arthritis, but there are no programs specific for hEDS/HSD.

• People with hEDS or HSD and healthcare professionals with experience in these conditions feel that an online pain management program specific to their condition is important; consensus revealed thirty-five key topics important to these stakeholders.

• The first hEDS/HSD-specific online pain management program, called HOPE, was developed with stakeholder input and usability tested, ready for clinical trial testing.

KeywordsDelphi; chronic pain; biopsychosocial; usability; connective tissue disorders
Year2025
JournalDisability and Rehabilitation
Journal citation47 (2), pp. 414-424
PublisherTaylor & Francis
ISSN0963-8288
Digital Object Identifier (DOI)https://doi.org/10.1080/09638288.2024.2351180
PubMed ID38738812
Scopus EID2-s2.0-85192834496
Open accessPublished as ‘gold’ (paid) open access
Page range414-424
FunderResearch Training Program Scholarship (RTP), Australian Government
Publisher's version
License
File Access Level
Open
Output statusPublished
Publication dates
Online13 May 2024
Publication process dates
Accepted26 Apr 2024
Deposited29 May 2025
Additional information

© 2024 The Author(s). Published by Informa UK Limtied, trading as Taylor & Francis Group.

This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent.

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