Informed consent is an important ethical factor for medicine, psychology, and other needed disciplines. It is necessary for participants to understand an intended research project or procedure in which they plan to take part. This study examined the usefulness of informed consent by administering such a form prior to an irrelevant questionnaire. A simple task was inserted into the reading, which allowed assessment of whether participants actually read the form. Results obtained through the experiment supported the hypothesis that the majority of the participants would not read the consent form. While less than half of each sex actually read the form, more women tended to read it than their male counterparts. Theoretical implications for the...
Abstract The informed consent form (ICF) is a document which explicitly confirms the consent of a pa...
Using a generic consent form is desirable in the informed-consent process, but such forms may not gi...
Background: Informed consent, a critical enabler of clinical research, depends on the provision of r...
Informed consent is an important ethical factor for medicine, psychology, and other needed disciplin...
This study examined the readability of 13 randomly selected informed consent forms used by researche...
Informed consent requires that potential clinical trial subjects be fully-informed and capable of ma...
Researchers typically attempt to fulfill disclosure and informed consent requirements by having part...
To conduct research ethically, informed consent must be obtained from each subject or a representati...
Background: Ethical problems most often arise in research. One of the most important ethical rules g...
Medical progress depends largely on experimentation involving human subjects. The informed consent d...
Background: The validity of the informed consent process rests in part on whether potential study pa...
Although many people choose to sign consent forms and participate in research, how many thoroughly r...
U.S. federal regulations, ICH guidelines, and good ethics require informed consent forms that potent...
Informed consent is important: in research, it allows subjects to make an informed and voluntary cho...
The aim of this study was to investigate the comprehension of Phase I healthy subjects after they ei...
Abstract The informed consent form (ICF) is a document which explicitly confirms the consent of a pa...
Using a generic consent form is desirable in the informed-consent process, but such forms may not gi...
Background: Informed consent, a critical enabler of clinical research, depends on the provision of r...
Informed consent is an important ethical factor for medicine, psychology, and other needed disciplin...
This study examined the readability of 13 randomly selected informed consent forms used by researche...
Informed consent requires that potential clinical trial subjects be fully-informed and capable of ma...
Researchers typically attempt to fulfill disclosure and informed consent requirements by having part...
To conduct research ethically, informed consent must be obtained from each subject or a representati...
Background: Ethical problems most often arise in research. One of the most important ethical rules g...
Medical progress depends largely on experimentation involving human subjects. The informed consent d...
Background: The validity of the informed consent process rests in part on whether potential study pa...
Although many people choose to sign consent forms and participate in research, how many thoroughly r...
U.S. federal regulations, ICH guidelines, and good ethics require informed consent forms that potent...
Informed consent is important: in research, it allows subjects to make an informed and voluntary cho...
The aim of this study was to investigate the comprehension of Phase I healthy subjects after they ei...
Abstract The informed consent form (ICF) is a document which explicitly confirms the consent of a pa...
Using a generic consent form is desirable in the informed-consent process, but such forms may not gi...
Background: Informed consent, a critical enabler of clinical research, depends on the provision of r...