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. 2020 Jul 8;18(1):76.
doi: 10.1186/s12961-020-00589-7.

Developing pathways for community-led research with big data: a content analysis of stakeholder interviews

Affiliations

Developing pathways for community-led research with big data: a content analysis of stakeholder interviews

Shira Grayson et al. Health Res Policy Syst. .

Abstract

Background: Big data (BD) informs nearly every aspect of our lives and, in health research, is the foundation for basic discovery and its tailored translation into healthcare. Yet, as new data resources and citizen/patient-led science movements offer sites of innovation, segments of the population with the lowest health status are least likely to engage in BD research either as intentional data contributors or as 'citizen/community scientists'. Progress is being made to include a more diverse spectrum of research participants in datasets and to encourage inclusive and collaborative engagement in research through community-based participatory research approaches, citizen/patient-led research pilots and incremental research policy changes. However, additional evidence-based policies are needed at the organisational, community and national levels to strengthen capacity-building and widespread adoption of these approaches to ensure that the translation of research is effectively used to improve health and health equity. The aims of this study are to capture uses of BD ('use cases') from the perspectives of community leaders and to identify needs and barriers for enabling community-led BD science.

Methods: We conducted a qualitative content analysis of semi-structured key informant interviews with 16 community leaders.

Results: Based on our analysis findings, we developed a BD Engagement Model illustrating the pathways and various forces for and against community engagement in BD research.

Conclusions: The goal of our Model is to promote concrete, transparent dialogue between communities and researchers about barriers and facilitators of authentic community-engaged BD research. Findings from this study will inform the subsequent phases of a multi-phased project with the ultimate aims of organising fundable frameworks and identifying policy options to support BD projects within community settings.

Keywords: Big Data; community engagement; community-led research; patient-led research; public health; qualitative analysis.

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Conflict of interest statement

MD is a co-inventor of the Cleveland Clinic’s MyLegacy intellectual property portfolio, now licensed to Family Care Path, Inc. As part of this license, she is entitled to a share in both royalties and returns on equity. JHY is a member of Sage Bionetworks Scientific Advisory Board.

Figures

Fig. 1
Fig. 1
Big Data (BD) Community Engagement Model. The model illustrates the various pathways by which communities engage in BD research, according to analysis findings from 16 key informant interviews. The factors that positively and negatively reinforce actions along a pathway are depicted in green and red, respectively

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