Cargando…
Readability of Participant Informed Consent Forms and Informational Documents: From Phase 3 COVID-19 Vaccine Clinical Trials in the United States
OBJECTIVE: To assess the readability of the informed consent forms from the phase 3 COVID-19 vaccine trials conducted in the United States. PATIENTS AND METHODS: English consent forms were used for patients in phase 3 COVID-19 vaccine clinical trials. Consent forms were obtained in October 2020. Usi...
Autores principales: | Bothun, Luke S., Feeder, Scott E., Poland, Gregory A. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mayo Foundation for Medical Education and Research
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8173482/ https://www.ncbi.nlm.nih.gov/pubmed/34226027 http://dx.doi.org/10.1016/j.mayocp.2021.05.025 |
Ejemplares similares
-
Readability of COVID-19 vaccine information for the general public
por: Bothun, Luke S., et al.
Publicado: (2022) -
The informed consent form navigator: a tool for producing readable and compliant consent documents
por: Bona, Jonathan P., et al.
Publicado: (2022) -
Readability of patient information and consent documents in rheumatological studies
por: Hamnes, Bente, et al.
Publicado: (2016) -
Assessment of Length and Readability of Informed Consent Documents for COVID-19 Vaccine Trials
por: Emanuel, Ezekiel J., et al.
Publicado: (2021) -
Readability and Comprehensibility of Informed Consent Forms for Clinical Trials
por: Pandiya, Anvita
Publicado: (2010)