Abstract

BackgroundPatient engagement in research (PEIR) is promoted to improve the relevance and quality of health research, but has little conceptualization derived from empirical data.ObjectiveTo address this issue, we sought to develop an empirically based conceptual framework for meaningful PEIR founded on a patient perspective.MethodsWe conducted a qualitative secondary analysis of in‐depth interviews with 18 patient research partners from a research centre‐affiliated patient advisory board. Data analysis involved three phases: identifying the themes, developing a framework and confirming the framework. We coded and organized the data, and abstracted, illustrated, described and explored the emergent themes using thematic analysis. Directed content analysis was conducted to derive concepts from 18 publications related to PEIR to supplement, confirm or refute, and extend the emergent conceptual framework. The framework was reviewed by four patient research partners on our research team.ResultsParticipants’ experiences of working with researchers were generally positive. Eight themes emerged: procedural requirements, convenience, contributions, support, team interaction, research environment, feel valued and benefits. These themes were interconnected and formed a conceptual framework to explain the phenomenon of meaningful PEIR from a patient perspective. This framework, the PEIR Framework, was endorsed by the patient research partners on our team.ConclusionsThe PEIR Framework provides guidance on aspects of PEIR to address for meaningful PEIR. It could be particularly useful when patient‐researcher partnerships are led by researchers with little experience of engaging patients in research.

Highlights

  • Patient engagement in research (PEIR) involves patients or their surrogates undertaking roles beyond those of traditional study participants along the continuum of the research process, including knowledge translation

  • The increased popularity of PEIR in the last 15 years coincides with a greater awareness among funding agencies that patients are key stakeholders of health research.[6,8,9,10]

  • This study aimed to develop a conceptual framework for meaningful PEIR from a patient perspective

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Summary

Introduction

Patient engagement in research (PEIR) involves patients or their surrogates undertaking roles beyond those of traditional study participants along the continuum of the research process, including knowledge translation. Eight themes emerged: procedural requirements, convenience, contributions, support, team interaction, research environment, feel valued and benefits. These themes were interconnected and formed a conceptual framework to explain the phenomenon of meaningful PEIR from a patient perspective. Conclusions: The PEIR Framework provides guidance on aspects of PEIR to address for meaningful PEIR It could be useful when patient-­researcher partnerships are led by researchers with little experience of engaging patients in research

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