Readability of health research informed consent forms: case of the National Health Research Ethics Committee in Tanzania.

IF 3 1区 哲学 Q1 ETHICS
Renatha Kato, Renatha Joseph, Lazaro Haule, Mwanaidi Kafuye
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引用次数: 0

Abstract

Background: Obtaining informed consent is the practice of respect for persons that gives the right to participants to make autonomous decisions about research participation. The difficult-to-read research informed consent forms (RICFs) hinder comprehension and can expose participants to harm. This study aims to assess the readability of health RICFs for studies approved by the National Health Research Ethics Committee (NatHREC) in Tanzania.

Methods: We used a retrospective cross-sectional study design. A total of 266 RICFs were sampled from the NatHREC database using stratified and systematic random sampling strategies. The readability of RICFs was assessed using the Flesch Reading Ease (FRE) and Flesch-Kincaid Readability Grade Level (FKRGL) formulas available in Microsoft Word Office and by manual check. Data were collected using the assessment checklist, analyzed, and presented with SPSS and MS Excel software.

Results: Out of 266 RICFs assessed, 65.4% had the recommended page numbers, 81.6% had longer sentences, and 80.5% were difficult to read, necessitating a person to acquire a US grade 10 (Form Four educational level in Tanzania) to understand the presented information. Pearson's correlation coefficient with p-values of < 0.001 and 95% confidence level disclosed that sentence lengths in the RICFs had a statistical association with the difficult reading levels obtained.

Conclusion: Findings from this study showed that most of the RICFs were concise in terms of page numbers and word count but had long and difficult sentences. Researchers should assess the readability of RICFs before submitting them for ethical approval. Research Ethics Committees (RECs) should consider inclusion of RICFs readability measurements in the Ethics Guidelines for Health Research. The study recommends further studies to assess the Kiswahili versions of RICFs to determine if the results obtained in this study apply to Kiswahili texts.

Clinical trial number: Not applicable.

卫生研究知情同意书的可读性:坦桑尼亚国家卫生研究伦理委员会的案例。
背景:获得知情同意是一种尊重人的做法,它赋予参与者自主决定参与研究的权利。难以阅读的研究知情同意书(RICFs)阻碍了理解,并可能使参与者受到伤害。本研究旨在评估坦桑尼亚国家卫生研究伦理委员会(NatHREC)批准的卫生ricf研究的可读性。方法:采用回顾性横断面研究设计。采用分层和系统随机抽样策略从NatHREC数据库中抽取266个ricf。使用Microsoft Word Office中提供的Flesch Reading Ease (FRE)和Flesch- kincaid readability Grade Level (FKRGL)公式和人工检查来评估RICFs的可读性。采用评估表收集数据,用SPSS和MS Excel软件进行分析和呈现。结果:在评估的266个ricf中,65.4%具有推荐页码,81.6%具有较长的句子,80.5%难以阅读,需要一个人获得美国10级(坦桑尼亚的四年级教育水平)才能理解所呈现的信息。结论的p值与Pearson的相关系数:本研究发现,大多数RICFs在页数和字数方面简洁,但句子长而难。研究人员应该在提交RICFs以获得伦理批准之前评估其可读性。研究伦理委员会(rec)应考虑将RICFs的可读性测量纳入卫生研究伦理准则。该研究建议进一步研究评估斯瓦希里语版本的RICFs,以确定本研究获得的结果是否适用于斯瓦希里语文本。临床试验号:不适用。
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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来源期刊
BMC Medical Ethics
BMC Medical Ethics MEDICAL ETHICS-
CiteScore
5.20
自引率
7.40%
发文量
108
审稿时长
>12 weeks
期刊介绍: BMC Medical Ethics is an open access journal publishing original peer-reviewed research articles in relation to the ethical aspects of biomedical research and clinical practice, including professional choices and conduct, medical technologies, healthcare systems and health policies.
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