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... Mehr ...

Verfasser: Schoemaker, Casper G
Armbrust, Wineke
Swart, Joost F
Vastert, Sebastiaan J
Loosdregt, Jorg van
Verwoerd, Anouk
Whiting, Caroline
Olsder, W
Versluis, Els
Vliet, Rens van
Fernhout, Marlous J
Bookelman, Sanne L
Cappon, Jeannette
Berg, J Merlijn van den
Schatorjé, Ellen
Muller, Petra C E Hissink
Kamphuis, Sylvia
Boer, Joke de
Lelieveld, Otto T H M
Net, Janjaap van der
Jongsma, Karin R
Rensen, Annemiek van
Dedding, Christine
Wulffraat, Nico M
Dokumenttyp: article / Letter to the editor
Erscheinungsdatum: 2018
Verlag/Hrsg.: BioMed Central
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-26674943
Datenquelle: BASE; Originalkatalog
Powered By: BASE
Link(s) : http://repository.tue.nl/905789