联合健康研究中的知情同意文件是否遵循国家指南?对提交给某三级保健医院机构伦理委员会的建议进行回顾性分析

Shilpshree Palsule, J. Shetye, M. Lad
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摘要

背景:知情同意过程是研究过程的重要组成部分。它保护参与者自由决定是否参与研究的自主权。预计知情同意文件(ICD)应以简单的术语和参与者理解的语言向参与者解释研究的性质和内容。研究者的责任是在每位参与者参与研究前获得其知情同意。目的:目的是评价一家三级保健医院的联合保健分院提交初步审查的研究的知情同意程序文件是否符合印度医学研究委员会(ICMR)的指导方针,以及它们是否与提交初步审查的方案有关。研究设计:这是一项回顾性研究。方法:经机构伦理委员会(IEC)批准,对2018年11月1日至2019年10月31日期间由联合医疗分支机构向Seth GS医学院和孟买三级医院KEM医院伦理委员会提交的所有研究进行审查。35个方案符合纳入标准。评估这些研究的icd是否符合ICMR 2017指南。注意并分析了伦理委员会对icd的评论。结果:根据ICMR 2017的生物医学健康研究规范,提交的35项研究中有34项包含了知情同意过程的所有10个强制性要点。7个方案没有完成审查过程,也没有收到许可信。IEC的询问主要涉及技术语言的使用、医学术语的简短形式、不恰当地提及风险和不适以及样本量。结论:本研究得出结论,根据ICMR 2017指南推荐的章节,所审查的icd是完整的。但是,调查人员和独立选举委员会都有某些失误,其中提交的国际分类报告没有传达研究的真实性质,独立选举委员会在审查时没有正确指出所有这些失误。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Does the informed consent document in allied health research follow the national guidelines? A retrospective analysis of proposals submitted to an institutional ethics committee of a tertiary care hospital
Background: Informed consent process forms an essential component of the research process. It protects participants' autonomy to decide whether or not to participate in the research freely. It is expected that the informed consent document (ICD) should explain the nature and content of the research to a participant in simple terminology and in the language that the participant understands. The researcher's responsibility is to obtain informed consent from every participant before his/her participation in the research. Objectives: The objective is to evaluate whether the informed consent process documents of research studies submitted for initial review by allied health branches of a tertiary care hospital follow the Indian Council of Medical Research (ICMR) guidelines and whether they relate to the protocol submitted for initial review. Study Design: This was a retrospective study. Methods: After institutional ethics committee (IEC) approval, all research studies submitted by allied health branches to the ethics committee of Seth GS Medical College and KEM Hospital, a tertiary care hospital in Mumbai, from November 1, 2018, to October 31, 2019, were reviewed. Thirty-five protocols were found to meet the inclusion criteria. The ICDs of these studies were evaluated for adherence to the ICMR 2017 guidelines. Ethics committee comments related to the ICDs were noted and analyzed. Results: 34 out of 35 research studies submitted had included all the ten mandatory points of the informed consent process, as per the Biomedical Health Research norms of the ICMR 2017. Seven protocols did not complete the review process and did not receive a letter of permission. IEC queries were mostly related to use of technical language, short forms of medical terms, improper mention of risks and discomforts, and sample size. Conclusion: This study concluded that the ICDs reviewed were complete in terms of sections recommended by the ICMR 2017 guidelines. However, there were certain lapses on the part of both the investigators and IEC, wherein the submitted ICDs did not convey the true nature of the study and the IEC did not correctly point out all these lapses at the time of the review.
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