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Assessment of Length and Readability of Informed Consent Documents for COVID-19 Vaccine Trials
IMPORTANCE: Informed consent is a fundamental element of research ethics. The COVID-19 vaccine trials are high profile trials that have enrolled more than 100 000 participants. Consent documents must be succinct and understandable to ensure informed voluntary participation. OBJECTIVE: To assess how...
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| Publicado no: | JAMA Netw Open |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Medical Association
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8082317/ https://ncbi.nlm.nih.gov/pubmed/33909052 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/jamanetworkopen.2021.10843 |
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