Content and Readability of Informed Consent Documents Approved by Research Ethics Committees of Health Institutions in South-East Nigeria.

Onyinye Chime, Emmanuel Ezeome
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Abstract

Variability and inadequacies in the contents of informed consent documents (ICDs) affect the quality of the informed consent (IC) process. This study assessed the content and readability of the 241 ICDs approved for biomedical research in South-East Nigeria from 2019 to 2021. The presence of basic elements for IC in the revised Common Rule and National Code was assessed, and the Flesh readability scores measured. Only 2 (0.8%) of the ICDs had all basic elements required by the Common Rule. Most ICDs fall below recommended readability indices. To improve the quality of the IC process, HRECs are to ensure that, while upholding research validity and credibility, ICDs are easy-to-read yet contain the basic information needed for decision-making by participants.

尼日利亚东南部卫生机构研究伦理委员会批准的知情同意文件的内容和可读性。
知情同意文件(ICDs)内容的多变性和不足影响了知情同意(IC)过程的质量。本研究评估了2019年至2021年尼日利亚东南部批准用于生物医学研究的241份icd的内容和可读性。对修订后的通用规则和国家代码中IC基本元素的存在进行了评估,并测量了Flesh可读性分数。只有2个(0.8%)icd具有共同规则要求的所有基本元素。大多数icd低于推荐的可读性指标。为了提高IC过程的质量,HRECs应确保icd在保持研究有效性和可信度的同时易于阅读,并包含参与者决策所需的基本信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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