Abstract The informed consent form (ICF) is a document which explicitly confirms the consent of a participant in a research project, and should contain all necessary information clarifying the study in which the subject intends to participate. This study evaluates the level of comprehension of an ICF signed by 146 volunteers using a self-administered instrument. The average age of the sample was 47.29 years, and there was a prevalence of women (67.2%), incomplete primary education (53.4%) and no private health care (93.2%). The mean score of correct answers of 146 respondents was 53.1%. There was no association between the percentage of correct answers and the variables of gender, age, education and time of response. There was a significant...
Background: Informed consent forms are required in all clinical trials which are approved by an inde...
Informed consent is an important ethical factor for medicine, psychology, and other needed disciplin...
Medical progress depends largely on experimentation involving human subjects. The informed consent d...
The signed informed consent form provides documentary evidence that the patient has given informed c...
To conduct research ethically, informed consent must be obtained from each subject or a representati...
The aim of this study was to investigate the comprehension of Phase I healthy subjects after they ei...
The process of informed consent remains a constant challenge in clinical research. The aim of the pr...
U.S. federal regulations, ICH guidelines, and good ethics require informed consent forms that potent...
ABSTRACT – Background: The written informed consent form (WICF) provides information that must be wr...
Informed consent requires that potential clinical trial subjects be fully-informed and capable of ma...
Information on the rights of subjects in clinical trials has become increasingly complex and difficu...
OBJECTIVE: Information on the rights of subjects in clinical trials has become increasingly complex ...
Background: Informed consent, a critical enabler of clinical research, depends on the provision of r...
Objective: Information on the rights of subjects in clinical trials has become increasingly complex ...
Writing an informed consent form (ICF) for biomedical research is a difficult task. We conducted a m...
Background: Informed consent forms are required in all clinical trials which are approved by an inde...
Informed consent is an important ethical factor for medicine, psychology, and other needed disciplin...
Medical progress depends largely on experimentation involving human subjects. The informed consent d...
The signed informed consent form provides documentary evidence that the patient has given informed c...
To conduct research ethically, informed consent must be obtained from each subject or a representati...
The aim of this study was to investigate the comprehension of Phase I healthy subjects after they ei...
The process of informed consent remains a constant challenge in clinical research. The aim of the pr...
U.S. federal regulations, ICH guidelines, and good ethics require informed consent forms that potent...
ABSTRACT – Background: The written informed consent form (WICF) provides information that must be wr...
Informed consent requires that potential clinical trial subjects be fully-informed and capable of ma...
Information on the rights of subjects in clinical trials has become increasingly complex and difficu...
OBJECTIVE: Information on the rights of subjects in clinical trials has become increasingly complex ...
Background: Informed consent, a critical enabler of clinical research, depends on the provision of r...
Objective: Information on the rights of subjects in clinical trials has become increasingly complex ...
Writing an informed consent form (ICF) for biomedical research is a difficult task. We conducted a m...
Background: Informed consent forms are required in all clinical trials which are approved by an inde...
Informed consent is an important ethical factor for medicine, psychology, and other needed disciplin...
Medical progress depends largely on experimentation involving human subjects. The informed consent d...