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一项关于在低收入环境中使用快速伦理评估来改善健康研究知情同意程序的认知的混合方法研究。

A mixed-methods study on perceptions towards use of Rapid Ethical Assessment to improve informed consent processes for health research in a low-income setting.

作者信息

Addissie Adamu, Davey Gail, Newport Melanie J, Addissie Thomas, MacGregor Hayley, Feleke Yeweyenhareg, Farsides Bobbie

机构信息

Brighton and Sussex Medical School, Falmer, UK.

出版信息

BMC Med Ethics. 2014 May 2;15:35. doi: 10.1186/1472-6939-15-35.

Abstract

BACKGROUND

Rapid Ethical Assessment (REA) is a form of rapid ethnographic assessment conducted at the beginning of research project to guide the consent process with the objective of reconciling universal ethical guidance with specific research contexts. The current study is conducted to assess the perceived relevance of introducing REA as a mainstream tool in Ethiopia.

METHODS

Mixed methods research using a sequential explanatory approach was conducted from July to September 2012, including 241 cross-sectional, self-administered and 19 qualitative, in-depth interviews among health researchers and regulators including ethics committee members in Ethiopian health research institutions and universities.

RESULTS

In their evaluation of the consent process, only 40.2% thought that the consent process and information given were adequately understood by study participants; 84.6% claimed they were not satisfied with the current consent process and 85.5% thought the best interests of study participants were not adequately considered. Commonly mentioned consent-related problems included lack of clarity (48.1%), inadequate information (34%), language barriers (28.2%), cultural differences (27.4%), undue expectations (26.6%) and power imbalances (20.7%). About 95.4% believed that consent should be contextualized to the study setting and 39.4% thought REA would be an appropriate approach to improve the perceived problems. Qualitative findings helped to further explore the gaps identified in the quantitative findings and to map-out concerns related to the current research consent process in Ethiopia. Suggestions included, conducting REA during the pre-test (pilot) phase of studies when applicable. The need for clear guidance for researchers on issues such as when and how to apply the REA tools was stressed.

CONCLUSION

The study findings clearly indicated that there are perceived to be correctable gaps in the consent process of medical research in Ethiopia. REA is considered relevant by researchers and stakeholders to address these gaps. Exploring further the feasibility and applicability of REA is recommended.

摘要

背景

快速伦理评估(REA)是在研究项目开始时进行的一种快速人种学评估形式,旨在指导知情同意过程,目的是使普遍的伦理指导与特定的研究背景相协调。本研究旨在评估在埃塞俄比亚引入REA作为一种主流工具的感知相关性。

方法

2012年7月至9月采用顺序解释性方法进行了混合方法研究,包括对埃塞俄比亚卫生研究机构和大学的卫生研究人员、监管人员(包括伦理委员会成员)进行241次横断面自填式调查和19次定性深入访谈。

结果

在对知情同意过程的评估中,只有40.2%的人认为研究参与者充分理解了知情同意过程和所提供的信息;84.6%的人声称他们对当前的知情同意过程不满意,85.5%的人认为没有充分考虑研究参与者的最大利益。常见的与知情同意相关的问题包括缺乏清晰度(48.1%)、信息不足(34%)、语言障碍(28.2%)、文化差异(27.4%)、过高期望(26.6%)和权力不平衡(20.7%)。约95.4%的人认为知情同意应根据研究背景进行调整,39.4%的人认为REA是改善所发现问题的合适方法。定性研究结果有助于进一步探索定量研究结果中发现的差距,并梳理出与埃塞俄比亚当前研究知情同意过程相关的问题。建议包括在适用时在研究的预试验(试点)阶段进行REA。强调了为研究人员提供关于何时以及如何应用REA工具等问题的明确指导的必要性。

结论

研究结果清楚地表明,埃塞俄比亚医学研究的知情同意过程中存在可纠正的差距。研究人员和利益相关者认为REA与解决这些差距相关。建议进一步探索REA的可行性和适用性。

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