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Volunteer experiences and perceptions of the informed consent process: Lessons from two HIV clinical trials in Uganda

BACKGROUND: Informed consent as stipulated in regulatory human research guidelines requires that a volunteer is well-informed about what will happen to them in a trial. However researchers are faced with a challenge of how to ensure that a volunteer agreeing to take part in a clinical trial is truly...

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Dades bibliogràfiques
Publicat a:BMC Med Ethics
Autors principals: Ssali, Agnes, Poland, Fiona, Seeley, Janet
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2015
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4668674/
https://ncbi.nlm.nih.gov/pubmed/26630924
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12910-015-0073-1
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