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...

Descripción completa

Detalles Bibliográficos
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:
Original Article
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

Internet

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