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Examining the Needs of Patient Stakeholders as Research Partners in Health Data Networks for Translational Research

机译:检查患者利益相关者作为健康数据网络中的研究合作伙伴以进行转化研究的需求

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摘要

Patient stakeholders are getting increasingly involved in research health data networks, particularly as research partners. However, tools do not exist to help effectively orient, educate, and engage patient stakeholders as they take on these roles. Using a human centered design approach, we conducted a patient stakeholder needs assessment qualitative study to identify key user needs to drive design recommendations for development of an online education and engagement tool for research health data networks. We found three key needs related to multiple role identities, motivations and expectations for participation on research teams, and patient journeys. Design recommendations derived from the needs assessment are discussed that can support future tool design and testing.
机译:患者利益相关者越来越多地参与研究健康数据网络,尤其是作为研究合作伙伴。但是,没有工具可以帮助患者利益相关者在担任这些角色时有效地定向,教育和吸引他们。使用以人为本的设计方法,我们进行了患者利益相关者需求评估定性研究,以识别关键用户需求,从而推动设计建议,以开发用于研究健康数据网络的在线教育和参与工具。我们发现了与多个角色身份,参与研究团队的动机和期望以及患者旅程有关的三个关键需求。讨论了从需求评估中得出的设计建议,这些建议可以支持将来的工具设计和测试。

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