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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 |
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| Hauptverfasser: | , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Public Library of Science
2017
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| 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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