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A randomized trial comparing concise and standard consent forms in the START trial

BACKGROUND: Improving the effectiveness and efficiency of research informed consent is a high priority. Some express concern about longer, more complex, written consent forms creating barriers to participant understanding. A recent meta-analysis concluded that randomized comparisons were needed. MET...

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Veröffentlicht in:PLoS One
Hauptverfasser: Grady, Christine, Touloumi, Giota, Walker, A. Sarah, Smolskis, Mary, Sharma, Shweta, Babiker, Abdel G., Pantazis, Nikos, Tavel, Jorge, Florence, Eric, Sanchez, Adriana, Hudson, Fleur, Papadopoulos, Antonios, Emanuel, Ezekiel, Clewett, Megan, Munroe, David, Denning, Eileen
Format: Artigo
Sprache:Inglês
Veröffentlicht: Public Library of Science 2017
Schlagworte:
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5406127/
https://ncbi.nlm.nih.gov/pubmed/28445471
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0172607
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