ArticleBMJ open2013
Facilitating and inhibiting factors for long-term involvement of patients at outcome conferences--lessons learnt from a decade of collaboration in OMERACT: a qualitative study.
Article in BMJ open, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
17 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Patient research partner involvement in rheumatology research: a systematic literature review informing the 2023 updated EULAR recommendations for the involvement of patient research partners.Annals of the rheumatic diseases · 2024Pooled it
- Building the future of patient-centred research: an EULAR PARE community of practice advancing patient research partner involvement in rheumatology.EULAR rheumatology open · 2026Article
- Article
- EULAR recommendations for the involvement of patient research partners in rheumatology research: 2023 update.Annals of the rheumatic diseases · 2024Article
- Patient and public involvement in research: a review of practical resources for young investigators.BMC rheumatology · 2023Review
- Making the patient voice heard in a research consortium: experiences from an EU project (IMI-APPROACH).Research involvement and engagement · 2021Article
- How the 10th ISDM Conference Got to Qualify as "Patients Included™": Insight from Inside.The patient · 2020Article
- Conducting research in psoriatic arthritis: the emerging role of patient research partners.Rheumatology (Oxford, England) · 2020Review
- 'Adding another spinning plate to an already busy lifeBMJ open · 2018Article
- Giving Voice to Patients: Developing a Discussion Method to Involve Patients in Translational Research.Nanoethics · 2018Article
- The Benefits of Patient Involvement for Translational Research.Health care analysis : HCA : journal of health philosophy and policy · 2017Review
- Patient Participation at Health Care Conferences: Engaged Patients Increase Information Flow, Expand Propagation, and Deepen Engagement in the Conversation of Tweets Compared to Physicians or Researchers.Journal of medical Internet research · 2017Article
- Establishing the values for patient engagement (PE) in health-related quality of life (HRQoL) research: an international, multiple-stakeholder perspective.Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation · 2017Article
- Successful Stepwise Development of Patient Research Partnership: 14 Years' Experience of Actions and Consequences in Outcome Measures in Rheumatology (OMERACT).The patient · 2017Article
- Patient and public engagement in health-related quality of life and patient-reported outcomes research: what is important and why should we care? Findings from the first ISOQOL patient engagement symposium.Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation · 2015Article
- Article
- Patient-centred healthcare outcome measures: towards a unified architecture.Journal of the Royal Society of Medicine · 2014Article
Corrections and comments
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
objectiveSeveral studies have provided insights into the conditions for successful patient involvement in health research. We recently demonstrated that long-term engagement with people with rheumatic conditions in international outcome research led to significant changes in the research agenda in the field of rheumatology. This article explores facilitating and inhibiting factors for long-term involvement of patients as collaborative partners at five Outcome Measures in Rheumatology (OMERACT) conferences.
designResponsive evaluation, starting with a thematic document analysis of conference proceedings and the grey literature, followed by 38 qualitative interviews. Interview transcripts were subjected to inductive content analysis.
setting5 international OMERACT conferences between 2002 and 2012.
participantsPatient delegates (n=16) and professional delegates representing researchers (n=14), pharmaceutical industry and regulators (n=2).
resultsCombined review of the document analysis and interview data revealed five main facilitators and three main barriers. Patient engagement as full participants at OMERACT conferences was enhanced by: strong leadership commitment and the presence of change agents, a clear selection procedure, an inclusive consensus-based conference design, individualised and self-organised support, an interactive and encouraging moderation style during discussion groups. Barriers were related to the intensity of the conference programme, scepticism among researchers and doubts about the representativeness of the patient group.
conclusionsThis study concludes that developing a sustainable structure for funding, selection and support of patient delegates, as well as adjusting conference design and moderation style, contributes not only towards facilitating direct dialogue between all stakeholders but also towards enhancing mutual understanding and the successful incorporation of the patient perspective in an outcome conference such as OMERACT.
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