نتایج جستجو برای: nocebo effect of informed consent
تعداد نتایج: 21212810 فیلتر نتایج به سال:
The problematic nature of informed consent to medical treatment and research, and its relation to autonomy, trust and clinical practice, has been addressed on many occasions and from a variety of ethical perspectives in the pages of the Journal of Medical Ethics. This paper gives an account of how discussion of these issues has developed and changed, by describing a number of significant contri...
Objectives Research has tended to focus on the information that researchers and ethicists deem important for informed consent to clinical trial participation and on the deficits in patients’ understanding of this information. Drawing on an alternative ‘capabilities’ approach we explored what information parents prioritised when making a decision about their child’s participation in a clinical t...
abstract background: gastroenterologists are required to obtain consent before undertaking any endoscopic examination. published data indicate that in practice there are many deficiencies in this process. the aim of this survey was to determine the quality of information given to patients before the endoscopic procedures in iran . methods: a structured questionnaire about patient's informed con...
Background: "Informed consent" is one of the most important issues in the medical ethics . Different points of view have proposed different opinions about it. In this Paper, we have reviewed different opinions and explained "Informed consent" based on Islamic view in Iran. In this article , we offered a review of the history, past studies and the components of the Informed consent an...
Researchers designing a clinical trial may be aware of disputed evidence of serious risks from previous studies. These researchers must decide whether and how to describe these risks in their model informed consent document. They have an ethical obligation to provide fully informed consent, but does this obligation include notice of controversial evidence? With ACCORD as an example, we describe...
Typically, a consent document in the United States is a printed form with blank spaces in which the operative procedure is filled in. The form is signed by the patient, and placed into the medical record. At first glance, it would seem that the patient was told of the operative procedure and gave his or her consent. Yet informed consent, or, more accurately, lack of informed consent, is a frequ...
Providing an informed consent has an important role in promotion of medical treatments and reduction of judiciary litigations in this process. Today with cultural changes and wide propagation that is usually charming, the request for aesthetic surgery has an increasing trend. These problems with complexity of cosmetic surgeries lead to deeper differences of information between plastic surgeons ...
نمودار تعداد نتایج جستجو در هر سال
با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید