2018
DOI: 10.1186/s40900-018-0099-x
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The prevalence of patient engagement in published trials: a systematic review

Abstract: Plain English summaryWith the growing movement to engage patients in research, questions are being asked about who is engaging patients and how they are being engaged. Internationally, research groups are supporting and funding patient-oriented research studies that engage patients in the identification of research priorities and the design, conduct and uptake of research. As we move forward, we need to know what meaningful patient engagement looks like, how it benefits research and clinical practice, and what… Show more

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Cited by 120 publications
(132 citation statements)
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“…In addition, CBPR principles and methods can inform PCOR designs. 6 Indeed, it is worth noting that, in the year after we began this study, a number of publications appeared that describe the scope, benefits, and challenges of patient engagement in health research. 7 This suggests that more health researchers are moving away from a "participants as subjects" standpoint to the practice of approaching participants as key stakeholders in clinical and health systems research, and these approaches may be informed by both PCOR and CBPR.…”
Section: E R H E R Hmentioning
confidence: 99%
See 1 more Smart Citation
“…In addition, CBPR principles and methods can inform PCOR designs. 6 Indeed, it is worth noting that, in the year after we began this study, a number of publications appeared that describe the scope, benefits, and challenges of patient engagement in health research. 7 This suggests that more health researchers are moving away from a "participants as subjects" standpoint to the practice of approaching participants as key stakeholders in clinical and health systems research, and these approaches may be informed by both PCOR and CBPR.…”
Section: E R H E R Hmentioning
confidence: 99%
“…The CBPR model involves researchers working with members of the relevant communities to identify research questions and develop the research design and also involves practices that treat research participants as experts and partners. In addition, CBPR principles and methods can inform PCOR designs 6 . Indeed, it is worth noting that, in the year after we began this study, a number of publications appeared that describe the scope, benefits, and challenges of patient engagement in health research 7 .…”
mentioning
confidence: 99%
“…Thus, there are many agencies and organizations created to support patient engagement with research. However, a recent systematic review on patient engagement with research found only 23 studies in all medical specialities in which the authors have reported patient engagement occurring at some stage in their research . This highlights the gap between aspiration and reality for patient engagement in research.…”
Section: Quotes From E‐mail Responses Of Bjd Editorial Board Membersmentioning
confidence: 99%
“…Much of the literature to date has focused on stakeholder engagement in specific tasks such as the development of research agendas or on the involvement of patients and other stakeholders across the phases of discreet CER and PCOR studies . However, effectively engaging stakeholders in the development and oversight of research infrastructure, as required for PCORnet, brings both distinct challenges and corresponding opportunities.…”
Section: Introductionmentioning
confidence: 99%
“…[6][7][8] Much of the literature to date has focused on stakeholder engagement in specific tasks such as the development of research agendas [9][10][11][12][13] or on the involvement of patients and other stakeholders across the phases of discreet CER and PCOR studies. [14][15][16][17] However, effectively engaging stakeholders in the development and oversight of research infrastructure, as required for PCORnet, brings both distinct challenges and corresponding opportunities. In this paper, we describe the process of establishing a Patient and Community Advisory Committee that ensure strict adherence to standards of data security, patient privacy, and research ethics.…”
mentioning
confidence: 99%