6544 Background: Informed consent forms (ICF) play an integral role in the consent process
for clinical trials (CT) by serving as a guide for discussion between the research team and …

Objectives: To compare the quality of informed consent forms (ICF) for different trial phases,
funding sources, oncology subspecialties, disease settings, and intervention modalities …

Purpose Efforts are underway in improving the informed consent process. The success of
these efforts to improve quality of informed consent forms (ICFs) for phase I oncology trials …

Aims: The purpose of this study was to analyze the content of informed consent forms for
clinical trials in medical oncology to assess readability, determine their completeness, and …

Background Informed consent forms (ICFs) for oncology clinical trials have grown
increasingly longer and more complex. We evaluated objective understanding of critical …

This study was conducted to assess the readability and length of informed consent
documents used in clinical trials in oncology. One hundred seven consent documents from …

Background The aim of the study was to investigate whether the length of informed consent
documents (ICDs) for oncological trials have increased from 1987 to 2007 and analyze the …

23 Background: The informed consent process is used to provide research participants
information that includes the purpose and procedures of the research study, risks, benefits …

Background Federal regulations state consent information should be understandable to
participants; concerns have been voiced about the quality of informed consent forms (ICFs) …

Background In respect of the principle of autonomy and the right of self-determination,
obtaining an informed consent of potential participants before their inclusion in a study is a …