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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5049790/ https://www.ncbi.nlm.nih.gov/pubmed/27701471 http://dx.doi.org/10.1371/journal.pone.0164251 |