Background: To facilitate informed consent, consent forms should use language below the grade eight level. Research Ethics Boards (REBs) provide consent form templates to facilitate this goal. Templates with inappropriate language could promote consent forms that participants find difficult to understand. However, a linguistic analysis of templates is lacking. Methods: We reviewed the websites of 124 REBs for their templates. These included English language medical school REBs in Australia/New Zealand (n=23), Canada (n=14), South Africa (n=8), the United Kingdom (n=34), and a geographically-stratified sample from the United States (n=45). Template language was analyzed using Coh-Metrix linguistic software (v.3.0, Memphis, USA). We evaluate...
Informed consent is crucial in research, but potential participants may not all speak the same langu...
As English is the predominant language of research protocols in the United States, non-English speak...
The scope of this project is to gauge the clinical researchers’ obtained knowledge of the consent fo...
Background: To facilitate informed consent, consent forms should use language below the grade eight ...
BACKGROUND:To facilitate informed consent, consent forms should use language below the grade eight l...
<div><p>Background</p><p>To facilitate informed consent, consent forms should use language below the...
Background: Understanding of informed consent forms (ICFs) for clinical research remains insufficien...
To conduct research ethically, informed consent must be obtained from each subject or a representati...
Background: Informed consent forms are required in all clinical trials which are approved by an inde...
National audienceOBJECTIVE: We compared informed consent forms of subjects participating in biomedic...
Obtaining informed consent (IC) is an ethical imperative, signifying participants’ understanding of ...
Advances in technology are increasing the risks of participating in educational technology research....
Informed choice is fundamentally a process of communication, reliant entirely on the tools of langua...
This data collection consists of 27 participant information sheets and 23 consent forms freely avail...
Writing an informed consent form (ICF) for biomedical research is a difficult task. We conducted a m...
Informed consent is crucial in research, but potential participants may not all speak the same langu...
As English is the predominant language of research protocols in the United States, non-English speak...
The scope of this project is to gauge the clinical researchers’ obtained knowledge of the consent fo...
Background: To facilitate informed consent, consent forms should use language below the grade eight ...
BACKGROUND:To facilitate informed consent, consent forms should use language below the grade eight l...
<div><p>Background</p><p>To facilitate informed consent, consent forms should use language below the...
Background: Understanding of informed consent forms (ICFs) for clinical research remains insufficien...
To conduct research ethically, informed consent must be obtained from each subject or a representati...
Background: Informed consent forms are required in all clinical trials which are approved by an inde...
National audienceOBJECTIVE: We compared informed consent forms of subjects participating in biomedic...
Obtaining informed consent (IC) is an ethical imperative, signifying participants’ understanding of ...
Advances in technology are increasing the risks of participating in educational technology research....
Informed choice is fundamentally a process of communication, reliant entirely on the tools of langua...
This data collection consists of 27 participant information sheets and 23 consent forms freely avail...
Writing an informed consent form (ICF) for biomedical research is a difficult task. We conducted a m...
Informed consent is crucial in research, but potential participants may not all speak the same langu...
As English is the predominant language of research protocols in the United States, non-English speak...
The scope of this project is to gauge the clinical researchers’ obtained knowledge of the consent fo...