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患者协会与临床肿瘤学研究:患者的声音到底有多重要?

Patient associations and clinical oncology research: how much does a patient's voice really matter?

机构信息

Medical Oncology Unit, A.O. Papardo Messina, Messina, Italy.

Unità Di Ricerca E Sviluppo Clinico S.C. Oncoematologia Pediatrica, AOU Città Della Salute E Della Scienza Presidio Ospedaliero Infantile Regina Margherita, Turin, Italy.

出版信息

Expert Rev Pharmacoecon Outcomes Res. 2021 Jun;21(3):433-440. doi: 10.1080/14737167.2021.1850274. Epub 2020 Nov 26.

Abstract

: New trends are emerging in clinical research, such as patient empowerment and an active role in influencing health and research ethics. Patients' involvement is considered pivotal by stakeholders and institutions because they can channel the voice of those they represent, empowering their starring role in the different research activities.: To obtain an overview of the real involvement of Italian patient associations in clinical research.: In January 2019, the Working Group 'Clinical Research Coordinators' of the Italian Association of Medical Oncology spread an online questionnaire consisting of 16 questions on the active involvement of patient associations in clinical research.: The involvement in clinical research working groups, in the organization and implementation of specific activities and training initiatives is very limited (21.7% in both cases), as well as the active involvement in the conduct and/or definition of clinical trials (0.3%). Moreover, few associations (15.2%) have joined projects on patient involvement in clinical research in collaboration with other associations.: Although the current involvement of the associations may have been somewhat underestimated, there is no doubt that much more can be done in terms of training and identification of common objectives between patients and professionals.

摘要

: 临床研究中出现了一些新趋势,例如患者赋权以及在影响健康和研究伦理方面发挥积极作用。利益相关者和机构认为患者的参与至关重要,因为他们可以为代表的人群发声,增强他们在不同研究活动中的主角地位。: 为了了解意大利患者协会在临床研究中的实际参与情况。: 2019 年 1 月,意大利肿瘤医学协会“临床研究协调员”工作组发布了一份在线问卷,共包含 16 个问题,涉及患者协会在临床研究中的积极参与情况。: 在临床研究工作组中的参与、组织和实施特定活动以及培训举措非常有限(两种情况均为 21.7%),而在临床试验的开展和/或定义中的积极参与则更少(0.3%)。此外,只有少数协会(15.2%)与其他协会合作参与了关于患者在临床研究中参与的项目。: 尽管目前协会的参与可能有些被低估,但在培训和确定患者与专业人员之间的共同目标方面,无疑还有很多工作要做。

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