Revised Common Rule Changes to the Consent Process and Consent Form
نویسندگان
چکیده
منابع مشابه
Informed consent readability: subject understanding of 15 common consent form phrases.
To conduct research ethically, informed consent must be obtained from each subject or a representative. This consent is documented when the patient signs an informed consent form. According to law, the requisite information for consent is to be presented in "language understandable to the subject or the representative." If consent forms are written in language that subjects do not fully underst...
متن کاملInforming the consent process.
Because the legal and ethical aspects of informed consent are often foremost in clinicians’ minds, it is easy to forget that the purpose of informed consent is to aid in decision making. Informed consent forms, for example, are often written with legal and institutional priorities in mind,1 and patients in turn assume that the primary purpose of such forms is to protect physicians and their ins...
متن کاملIeee Copyright and Consent Form
The trend in architectural designs has been towards using simple cores for building multicore chips, instead of a single complex out-of-order (OOO) cores, due to the increased complexity and energy requirements of out of order processors. Multicore chips provide better performance when compared with OOO cores while executing parallel applications. However, they are not able to exploit the paral...
متن کاملIeee Copyright and Consent Form
This paper investigates the statistical detection of Jsteg steganography. The approach is based on the statistical model of Discrete Cosine Transformation (DCT) coefficients. The hidden information detection problem is case in the framework of Hypothesis testing theory. In an ideal context where all model parameters are perfectly known, the Likelihood Ratio Test (LRT) is presented and its perfo...
متن کاملImproving the quality of consent to randomised controlled trials by using continuous consent and clinician training in the consent process.
OBJECTIVE To assess whether continuous consent, a process in which information is given to research participants at different stages in a trial, and clinician training in that process were effective when used by clinicians while gaining consent to the Total Body Hypothermia (TOBY) trial. The TOBY trial is a randomised controlled trial (RCT) investigating the use of whole-body cooling for neonat...
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ژورنال
عنوان ژورنال: Ochsner Journal
سال: 2020
ISSN: 1524-5012,1524-5012
DOI: 10.31486/toj.19.0055