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利用帕金森病患者代言人:一种用于患者参与的拟议框架,以及可确定其成功的现代衡量标准。

Utilizing patient advocates in Parkinson's disease: A proposed framework for patient engagement and the modern metrics that can determine its success.

机构信息

Parkinson's Foundation, New York, New York.

Section of Movement Disorders, Department of Neurological Sciences, Rush University Medical Center, Chicago, Illinois.

出版信息

Health Expect. 2020 Aug;23(4):722-730. doi: 10.1111/hex.13064. Epub 2020 May 3.

Abstract

The wide application of patient engagement and its associated benefits has increased across government, academic and pharmaceutical research. However, neither an identified standard practice for the process of engagement, nor utilization of common metrics to assess associated outcomes, exists. Parkinson's Foundation developed a patient engagement framework and metrics to assess engagement within the academic research and drug development sectors. This approach was developed over the course of several years through assessing the literature, acquiring feedback from researchers and people with Parkinson's disease and adapting practices to be relevant and generalizable across patient engagement projects. This framework includes the: 1) creation of a scope of work, 2) establishment of guiding principles, 3) selection and training of participants, 4) co-determination of project metrics, 5) execution of the project and 6) dissemination of project findings. Parkinson's Foundation has also worked with academic, government and pharmaceutical stakeholders to identify metrics that assess both the quality of patient engagement and outcomes associated with patient engagement on projects. By improving patient engagement project methodologies and metrics, global clinical trials can have access to evidence-based patient engagement practices to more efficiently capture the needs of, and potentially benefit, the patient community.

摘要

患者参与及其相关益处已经在政府、学术和制药研究领域得到广泛应用。然而,既没有确定的参与流程标准实践,也没有使用通用指标来评估相关结果。帕金森基金会开发了一个患者参与框架和指标,用于评估学术研究和药物开发领域的参与度。这种方法是通过多年来评估文献、从研究人员和帕金森病患者那里获得反馈以及调整实践以使其在患者参与项目中具有相关性和普遍性来制定的。该框架包括:1)制定工作范围,2)确立指导原则,3)选择和培训参与者,4)共同确定项目指标,5)执行项目,6)传播项目发现。帕金森基金会还与学术、政府和制药利益相关者合作,确定了评估项目中患者参与质量和与患者参与相关结果的指标。通过改进患者参与项目的方法和指标,全球临床试验可以采用基于证据的患者参与实践,更有效地了解患者群体的需求,并有可能使他们受益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fee7/7495075/fab9857a9bb1/HEX-23-722-g001.jpg

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