Literature DB >> 21257615

European League Against Rheumatism recommendations for the inclusion of patient representatives in scientific projects.

M P T de Wit1, S E Berlo, G J Aanerud, D Aletaha, J W Bijlsma, L Croucher, J A P Da Silva, B Glüsing, L Gossec, S Hewlett, M Jongkees, D Magnusson, M Scholte-Voshaar, P Richards, C Ziegler, T A Abma.   

Abstract

OBJECTIVE: To develop recommendations to enable successful inclusion of the patient perspective in European League Against Rheumatism (EULAR)-funded scientific research projects.
METHODS: The EULAR standardised operational procedures for guideline development were followed. A systematic literature review was presented during a first task force meeting, including 3 rheumatologists, 1 rheumatologist/epidemiologist, 2 allied health professionals, 2 representatives of arthritis research organisations and 7 patient representatives, resulting in 38 statements. A Delphi method was carried out to reduce and refine the statements and agree on a set of eight. Next, a survey among a wider group of experts, professionals and patient representatives (n=42), was completed. Feedback from this wider group was discussed at the second meeting and integrated in the final wording of the recommendations. Subsequently, the level of agreement of the group of experts (n=81) was re-evaluated.
RESULTS: The project resulted in a definition of patient research partner and agreement on a set of eight recommendations for their involvement in research projects. These recommendations provide practical guidance for organising patient participation, capturing (1) the role of patient research partners, (2) phase of involvement, (3) the recommended number, (4) recruitment, (5) selection, (6) support, (7) training and (8) acknowledgement.
CONCLUSION: Collaboration between patients and professionals in research is relatively new. Trials or effectiveness studies are not yet available. Nevertheless, it is possible to define recommendations for the inclusion of patients in research following a solid expert opinion based consensus process.

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Year:  2011        PMID: 21257615     DOI: 10.1136/ard.2010.135129

Source DB:  PubMed          Journal:  Ann Rheum Dis        ISSN: 0003-4967            Impact factor:   19.103


  93 in total

Review 1.  Framework for Advancing the Reporting of Patient Engagement in Rheumatology Research Projects.

Authors:  Clayon B Hamilton; Jenny C Leese; Alison M Hoens; Linda C Li
Journal:  Curr Rheumatol Rep       Date:  2017-07       Impact factor: 4.592

Review 2.  Patient reported outcomes in rheumatoid arthritis clinical trials.

Authors:  Ana-Maria Orbai; Clifton O Bingham
Journal:  Curr Rheumatol Rep       Date:  2015-04       Impact factor: 4.592

3.  The feasibility of an exercise intervention to improve sleep (time, quality and disturbance) in people with rheumatoid arthritis: a pilot RCT.

Authors:  Sean G McKenna; Alan Donnelly; Bente Appel Esbensen; Laura Comber; Wan Lin Ng; Aqeel Maqsoon Anjum; Alexander Fraser; Norelee M Kennedy
Journal:  Rheumatol Int       Date:  2021-01-02       Impact factor: 2.631

Review 4.  Practical Considerations for Using Online Methods to Engage Patients in Guideline Development.

Authors:  Sean Grant; Glen S Hazlewood; Holly L Peay; Ann Lucas; Ian Coulter; Arlene Fink; Dmitry Khodyakov
Journal:  Patient       Date:  2018-04       Impact factor: 3.883

Review 5.  Management of psoriatic arthritis in 2016: a comparison of EULAR and GRAPPA recommendations.

Authors:  Laure Gossec; Laura C Coates; Maarten de Wit; Arthur Kavanaugh; Sofia Ramiro; Philip J Mease; Christopher T Ritchlin; Désirée van der Heijde; Josef S Smolen
Journal:  Nat Rev Rheumatol       Date:  2016-11-10       Impact factor: 20.543

Review 6.  Patient-reported outcomes in core domain sets for rheumatic diseases.

Authors:  Lilian H D van Tuyl; Maarten Boers
Journal:  Nat Rev Rheumatol       Date:  2015-09-01       Impact factor: 20.543

7.  The impact of exercise on sleep (time, quality, and disturbance) in patients with rheumatoid arthritis: a study protocol for a pilot randomised controlled trial.

Authors:  Sean G McKenna; Alan E Donnelly; Bente A Esbensen; Alexander D Fraser; Norelee M Kennedy
Journal:  Rheumatol Int       Date:  2018-05-15       Impact factor: 2.631

8.  "Stiffness has different meanings, I think, to everyone": examining stiffness from the perspective of people living with rheumatoid arthritis.

Authors:  Ana-Maria Orbai; Katherine C Smith; Susan J Bartlett; Elaine De Leon; Clifton O Bingham
Journal:  Arthritis Care Res (Hoboken)       Date:  2014-11       Impact factor: 4.794

9.  "If i wasn't this robust": patients' expectations and experiences at the Outcome Measures in Rheumatology Conference 2010.

Authors:  Maarten P T de Wit; Marije S Koelewijn-van Loon; Sarah Collins; Tineke A Abma; John Kirwan
Journal:  Patient       Date:  2013       Impact factor: 3.883

10.  Do not forget the professional--the value of the FIRST model for guiding the structural involvement of patients in rheumatology research.

Authors:  Maarten P T de Wit; Janneke E Elberse; Jacqueline E W Broerse; Tineke A Abma
Journal:  Health Expect       Date:  2013-01-31       Impact factor: 3.377

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