Informed consent procedure in a double blind randomized anthelminthic trial on Pemba Island, Tanzania: do pamphlet and information session increase caregivers knowledge?

BACKGROUND: In clinical research, obtaining informed consent from participants is an ethical and legal requirement. Conveying the information concerning the study can be done using multiple methods yet this step commonly relies exclusively on the informed consent form alone. While this is legal, it...

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Detalles Bibliográficos
Autores principales: Palmeirim, Marta S., Ross, Amanda, Obrist, Brigit, Mohammed, Ulfat A., Ame, Shaali M., Ali, Said M., Keiser, Jennifer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6945786/
https://www.ncbi.nlm.nih.gov/pubmed/31906925
http://dx.doi.org/10.1186/s12910-019-0441-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6945786/
https://www.ncbi.nlm.nih.gov/pubmed/31906925
http://dx.doi.org/10.1186/s12910-019-0441-3

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