Kelly R. Tan, is PhD Student, School of Nursing, University of North Carolina at Chapel Hill. Mary K. Killela, is PhD Student, School of Nursing, University of North Carolina at Chapel Hill. Jill Leckey, is PhD Student, School of Nursing, University of North Carolina at Chapel Hill.
Nurs Res. 2021 Jan/Feb;70(1):67-71. doi: 10.1097/NNR.0000000000000473.
Social media platforms are useful for recruiting hard-to-reach populations, such as caregivers of children with cancer, for research. However, there are unique ethical considerations in using social media.
The aim of the study was to describe the methods used to recruit hard-to-reach caregivers (parents of children with cancer) for research and related ethical considerations.
We used The Belmont Report tenets (respect for persons, beneficence, and justice) as a guiding framework to identify issues relevant to social media recruitment of hard-to-reach populations and to describe how we addressed these issues in our study.
We engaged leaders of two online communities that offer peer support for caregivers of children with cancer to help with recruitment to our study on financial effect of pediatric cancer. We identified issues in using social media for recruiting hard-to-reach populations in alignment with The Belmont Report, including risk for subject selection bias, privacy rights, protecting identity of participants, data security issues, and access to research. We addressed issues by deliberate study design decisions and engagement with online community advocates.
Using social media to recruit hard-to-reach populations may be a successful way to engage them in research. Although researchers may remain compliant with the institutional review board of their facilities and are faithful to the tenets of The Belmont Report, unanticipated ethical issues may arise directly or indirectly as a result of using social media. This article identifies these issues and provides suggestions for dealing with them.
社交媒体平台对于招募难以接触到的人群(如癌症患儿的照顾者)参与研究非常有用。然而,在使用社交媒体时,存在着独特的伦理考虑因素。
本研究旨在描述招募难以接触到的照顾者(癌症患儿的父母)参与研究的方法以及相关的伦理考虑。
我们以《贝尔蒙报告》的原则(尊重个人、善行和公正)为指导框架,确定与社交媒体招募难以接触到的人群相关的问题,并描述我们在研究中如何解决这些问题。
我们与两个为癌症患儿照顾者提供同行支持的在线社区的领导者合作,以帮助我们招募参加我们关于儿科癌症经济影响的研究。我们确定了在使用社交媒体招募难以接触到的人群时与《贝尔蒙报告》一致的问题,包括受试者选择偏差的风险、隐私权、参与者身份的保护、数据安全问题以及对研究的访问。我们通过精心设计的研究决策和与在线社区倡导者的合作来解决这些问题。
使用社交媒体招募难以接触到的人群可能是一种成功的方式,可以使他们参与研究。尽管研究人员可能仍然遵守其机构审查委员会的规定,并忠实于《贝尔蒙报告》的原则,但由于使用社交媒体,可能会直接或间接地出现意想不到的伦理问题。本文确定了这些问题,并提出了处理这些问题的建议。