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Dutch juvenile idiopathic arthritis patients, carers and clinicians create a research agenda together following the James Lind Alliance method: A study protocol

Dutch juvenile idiopathic arthritis patients, carers and clinicians create a research agenda together following the James Lind Alliance method: A study protocol
Dutch juvenile idiopathic arthritis patients, carers and clinicians create a research agenda together following the James Lind Alliance method: A study protocol

Background: Research on Juvenile Idiopathic Arthritis (JIA) should support patients, caregivers/parents (carers) and clinicians to make important decisions in the consulting room and eventually to improve the lives of patients with JIA. Thus far these end-users of JIA-research have rarely been involved in the prioritisation of future research. Main body: Dutch organisations of patients, carers and clinicians will collaboratively develop a research agenda for JIA, following the James Lind Alliance (JLA) methodology. In a 'Priority Setting Partnership' (PSP), they will gradually establish a top 10 list of the most important unanswered research questions for JIA. In this process the input from clinicians, patients and their carers will be equally valued. Additionally, focus groups will be organised to involve young people with JIA. The involvement of all contributors will be monitored and evaluated. In this manner, the project will contribute to the growing body of literature on how to involve young people in agenda setting in a meaningful way. Conclusion: A JIA research agenda established through the JLA method and thus co-created by patients, carers and clinicians will inform researchers and research funders about the most important research questions for JIA. This will lead to research that really matters.

James Lind Alliance, Juvenile Idiopathic Arthritis (JIA), Patient involvement, Research agenda
Schoemaker, Casper G.
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Armbrust, Wineke
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Swart, Joost F.
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Vastert, Sebastiaan J.
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Van Loosdregt, Jorg
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Verwoerd, Anouk
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Whiting, Caroline
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Cowan, Katherine
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Olsder, Wendy
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Versluis, Els
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Van Vliet, Rens
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Fernhout, Marlous J.
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Bookelman, Sanne L.
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Cappon, Jeannette
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Van Den Berg, J. Merlijn
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Schatorjé, Ellen
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Muller, Petra C.E.Hissink
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Kamphuis, Sylvia
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De Boer, Joke
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Lelieveld, Otto T.H.M.
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Van Der Net, Janjaap
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Jongsma, Karin R.
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Van Rensen, Annemiek
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Dedding, Christine
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Wulffraat, Nico M.
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Schoemaker, Casper G.
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Armbrust, Wineke
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Swart, Joost F.
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Vastert, Sebastiaan J.
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Van Loosdregt, Jorg
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Verwoerd, Anouk
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Whiting, Caroline
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Cowan, Katherine
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Olsder, Wendy
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Versluis, Els
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Van Vliet, Rens
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Fernhout, Marlous J.
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Bookelman, Sanne L.
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Cappon, Jeannette
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Van Den Berg, J. Merlijn
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Schatorjé, Ellen
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Muller, Petra C.E.Hissink
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Kamphuis, Sylvia
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De Boer, Joke
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Lelieveld, Otto T.H.M.
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Van Der Net, Janjaap
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Jongsma, Karin R.
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Van Rensen, Annemiek
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Dedding, Christine
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Wulffraat, Nico M.
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Schoemaker, Casper G., Armbrust, Wineke, Swart, Joost F., Vastert, Sebastiaan J., Van Loosdregt, Jorg, Verwoerd, Anouk, Whiting, Caroline, Cowan, Katherine, Olsder, Wendy, Versluis, Els, Van Vliet, Rens, Fernhout, Marlous J., Bookelman, Sanne L., Cappon, Jeannette, Van Den Berg, J. Merlijn, Schatorjé, Ellen, Muller, Petra C.E.Hissink, Kamphuis, Sylvia, De Boer, Joke, Lelieveld, Otto T.H.M., Van Der Net, Janjaap, Jongsma, Karin R., Van Rensen, Annemiek, Dedding, Christine and Wulffraat, Nico M. (2018) Dutch juvenile idiopathic arthritis patients, carers and clinicians create a research agenda together following the James Lind Alliance method: A study protocol. Pediatric Rheumatology, 16 (1), [57]. (doi:10.1186/s12969-018-0276-3).

Record type: Review

Abstract

Background: Research on Juvenile Idiopathic Arthritis (JIA) should support patients, caregivers/parents (carers) and clinicians to make important decisions in the consulting room and eventually to improve the lives of patients with JIA. Thus far these end-users of JIA-research have rarely been involved in the prioritisation of future research. Main body: Dutch organisations of patients, carers and clinicians will collaboratively develop a research agenda for JIA, following the James Lind Alliance (JLA) methodology. In a 'Priority Setting Partnership' (PSP), they will gradually establish a top 10 list of the most important unanswered research questions for JIA. In this process the input from clinicians, patients and their carers will be equally valued. Additionally, focus groups will be organised to involve young people with JIA. The involvement of all contributors will be monitored and evaluated. In this manner, the project will contribute to the growing body of literature on how to involve young people in agenda setting in a meaningful way. Conclusion: A JIA research agenda established through the JLA method and thus co-created by patients, carers and clinicians will inform researchers and research funders about the most important research questions for JIA. This will lead to research that really matters.

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Accepted/In Press date: 10 September 2018
e-pub ahead of print date: 15 September 2018
Published date: 15 September 2018
Keywords: James Lind Alliance, Juvenile Idiopathic Arthritis (JIA), Patient involvement, Research agenda

Identifiers

Local EPrints ID: 424109
URI: http://eprints.soton.ac.uk/id/eprint/424109
PURE UUID: e1c37a23-8558-439e-a246-ae0c172b5122

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Date deposited: 04 Oct 2018 16:30
Last modified: 15 Apr 2024 17:06

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Contributors

Author: Casper G. Schoemaker
Author: Wineke Armbrust
Author: Joost F. Swart
Author: Sebastiaan J. Vastert
Author: Jorg Van Loosdregt
Author: Anouk Verwoerd
Author: Caroline Whiting
Author: Katherine Cowan
Author: Wendy Olsder
Author: Els Versluis
Author: Rens Van Vliet
Author: Marlous J. Fernhout
Author: Sanne L. Bookelman
Author: Jeannette Cappon
Author: J. Merlijn Van Den Berg
Author: Ellen Schatorjé
Author: Petra C.E.Hissink Muller
Author: Sylvia Kamphuis
Author: Joke De Boer
Author: Otto T.H.M. Lelieveld
Author: Janjaap Van Der Net
Author: Karin R. Jongsma
Author: Annemiek Van Rensen
Author: Christine Dedding
Author: Nico M. Wulffraat

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