Background: Understanding of informed consent forms (ICFs) for clinical research remains insufficient despite attempts to simplify them. Through linguistic discourse analysis, we sought to identify pitfalls within the text of ICFs that could hinder readers' understanding of participation in research. Methods: We conducted a linguistic discourse analysis on a qualitative sample of 19 ICFs approved by research ethics committees (RECs) for oncology protocols and explored whether our findings also applied to standard U.S. documents available online. Results: We identified five major categories of language patterns that were problematic with respect to ensuring informed consent. We categorized them as follows: “bypassing consent,” “seeker–suppli...
BACKGROUND:Informed consent forms (ICFs) for oncology clinical trials have grown increasingly longer...
The scope of this project is to gauge the clinical researchers’ obtained knowledge of the consent fo...
Importance. Oncology trials often entail high-stakes interventions where potential for morbidity and...
BACKGROUND:To facilitate informed consent, consent forms should use language below the grade eight l...
Background: To facilitate informed consent, consent forms should use language below the grade eight ...
<div><p>Background</p><p>To facilitate informed consent, consent forms should use language below the...
Obtaining informed consent (IC) is an ethical imperative, signifying participants’ understanding of ...
Informed consent often fails to meet the intended goals that a prospective subject should understand...
To conduct research ethically, informed consent must be obtained from each subject or a representati...
Informed consent often fails to meet the intended goals that a prospective subject should understand...
This data collection consists of 27 participant information sheets and 23 consent forms freely avail...
Informed consent documents (ICDs or “consent forms”) are a founding ethical principle of human subje...
Aims: The purpose of this study was to analyze the content of informed consent forms for clinical tr...
Informed consent forms (ICFs) for oncology clinical trials have grown increasingly longer and more c...
It is the researcher’s responsibility to provide accurate, complete, and unbiased verbal and written...
BACKGROUND:Informed consent forms (ICFs) for oncology clinical trials have grown increasingly longer...
The scope of this project is to gauge the clinical researchers’ obtained knowledge of the consent fo...
Importance. Oncology trials often entail high-stakes interventions where potential for morbidity and...
BACKGROUND:To facilitate informed consent, consent forms should use language below the grade eight l...
Background: To facilitate informed consent, consent forms should use language below the grade eight ...
<div><p>Background</p><p>To facilitate informed consent, consent forms should use language below the...
Obtaining informed consent (IC) is an ethical imperative, signifying participants’ understanding of ...
Informed consent often fails to meet the intended goals that a prospective subject should understand...
To conduct research ethically, informed consent must be obtained from each subject or a representati...
Informed consent often fails to meet the intended goals that a prospective subject should understand...
This data collection consists of 27 participant information sheets and 23 consent forms freely avail...
Informed consent documents (ICDs or “consent forms”) are a founding ethical principle of human subje...
Aims: The purpose of this study was to analyze the content of informed consent forms for clinical tr...
Informed consent forms (ICFs) for oncology clinical trials have grown increasingly longer and more c...
It is the researcher’s responsibility to provide accurate, complete, and unbiased verbal and written...
BACKGROUND:Informed consent forms (ICFs) for oncology clinical trials have grown increasingly longer...
The scope of this project is to gauge the clinical researchers’ obtained knowledge of the consent fo...
Importance. Oncology trials often entail high-stakes interventions where potential for morbidity and...