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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...
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| 出版年: | PLoS One |
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| 主要な著者: | , , , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Public Library of Science
2016
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| 主題: | |
| オンライン･アクセス: | 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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