Readability and Content Assessment of Informed Consent Forms for Phase II-IV Clinical Trials in China

PURPOSE: To explore the readability and content integrity of informed consent forms (ICFs) used in China and to compare the quality of Chinese local ICFs with that of international ICFs. METHODS: The length, readability and content of 155 consent documents from phase II-IV drug clinical trials from...

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Gepubliceerd in:PLoS One
Hoofdauteurs: Wen, Gaiyan, Liu, Xinchun, Huang, Lihua, Shu, Jingxian, Xu, Nana, Chen, Ruifang, Huang, Zhijun, Yang, Guoping, Wang, Xiaomin, Xiang, Yuxia, Lu, Yao, Yuan, Hong
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Public Library of Science 2016
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Research Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5049790/
https://ncbi.nlm.nih.gov/pubmed/27701471
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0164251
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