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Patient and public involvement in a UK National Institute for Health Research Programme Grant for Applied Research : experiences from the Chronic Headache Education and Self-management Study (CHESS)
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Nichols, Vivien P., Pearce, Gemma, Ellard, David R., Evans, Simon, Haywood, Kirstie L., Norman, Chloe, Potter, Rachel, Sandhu, Harbinder, Stewart, Kimberley, Underwood, Martin and Patel, Shilpa (2021) Patient and public involvement in a UK National Institute for Health Research Programme Grant for Applied Research : experiences from the Chronic Headache Education and Self-management Study (CHESS). Primary Health Care Research & Development, 22 . e72. doi:10.1017/S1463423621000670
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Official URL: http://dx.doi.org/10.1017/S1463423621000670
Abstract
Background:
Patient and public involvement (PPI) plays a crucial role in ensuring research is carried out in conjunction with the people that it will impact upon. In this article, we present our experiences and reflections from working collaboratively with patients and public through the lifetime of an National Institute for Health Research (NIHR) programme grant; the Chronic Headache Education and Self-management Study (CHESS) which took place between 2015 and 2020.
PPI over the course of CHESS:
We worked closely with three leading UK migraine charities and a lay advisory group throughout the programme. We followed NIHR standards and used the Guidance for Reporting Involvement of Patients and the Public checklist. We consulted our PPI contacts using a variety of methods depending on the phase of the study and the nature of the request. This included emails, discussions, and face-to-face contact.
PPI members contributed throughout the study in the programme development, in the grant application, ethics documentation, and trial oversight. During the feasibility study; in supporting the development of a classification interview for chronic headache by participating in a headache classification conference, assessing the relevance, and acceptability of patient-reported outcome measures by helping to analyse cognitive interview data, and testing the smartphone application making suggestions on how best to present the summary of data collected for participants. Due to PPI contribution, the content and duration of the study intervention were adapted and a Delphi study with consensus meeting developed a core outcome set for migraine studies.
Conclusions:
The involvement of the public and patients in CHESS has allowed us to shape its overall design, intervention development, and establish a core outcome set for future migraine studies. We have reflected on many learning points for the future application of PPI.
| Item Type: | Journal Article | |||||||||
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| Subjects: | R Medicine > R Medicine (General) R Medicine > RB Pathology R Medicine > RC Internal medicine |
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| Divisions: | Faculty of Medicine > Warwick Medical School > Health Sciences > Clinical Trials Unit Faculty of Medicine > Warwick Medical School > Health Sciences Faculty of Medicine > Warwick Medical School |
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| Library of Congress Subject Headings (LCSH): | Headache -- Diagnosis, Headache -- Prognosis, Headache -- Treatment, Chronic pain, Patient participation, Head -- Diseases | |||||||||
| Journal or Publication Title: | Primary Health Care Research & Development | |||||||||
| Publisher: | Cambridge University Press | |||||||||
| ISSN: | 1463-4236 | |||||||||
| Official Date: | 2021 | |||||||||
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| Volume: | 22 | |||||||||
| Article Number: | e72 | |||||||||
| DOI: | 10.1017/S1463423621000670 | |||||||||
| Status: | Peer Reviewed | |||||||||
| Publication Status: | Published | |||||||||
| Access rights to Published version: | Open Access | |||||||||
| RIOXX Funder/Project Grant: |
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| Contributors: |
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