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Measuring the Process and Quality of Informed Consent for Clinical Research: Development and Testing

PURPOSE/OBJECTIVES: To develop and assess the reliability and validity of an observational instrument, the Process and Quality of Informed Consent (P-QIC). DESIGN: A pilot study of the psychometrics of a tool designed to measure the quality and process of the informed consent encounter in clinical r...

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Hlavní autoři: Cohn, Elizabeth Gross, Jia, Haomiao, Smith, Winifred Chapman, Erwin, Katherine, Larson, Elaine L.
Médium: Artigo
Jazyk:Inglês
Vydáno: 2011
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3638913/
https://ncbi.nlm.nih.gov/pubmed/21708532
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1188/11.ONF.417-422
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