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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Dades bibliogràfiques
Publicat a:BMC Med Ethics
Autors principals: Palmeirim, Marta S., Ross, Amanda, Obrist, Brigit, Mohammed, Ulfat A., Ame, Shaali M., Ali, Said M., Keiser, Jennifer
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2020
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6945786/
https://ncbi.nlm.nih.gov/pubmed/31906925
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12910-019-0441-3
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