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Consent, Informed Consent and the Consent Form

New England Journal of Medicine, 1978
The unpermitted, unprivileged touching of the person of another is a legal wrong or, technically, a battery. The defense to a charge of battery is consent. In the nonemergency medical encounter, however, such consent is ineffective as a defense1 without a full understanding of what it is that is being consented to.
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Broad Consent Is Consent for Governance

The American Journal of Bioethics, 2015
In recent years, novel types of consent have been proposed for research with biological samples, one of these being broad consent.
Sarah N, Boers   +2 more
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Consent, Informed Consent

2021
Informed consent refers to patients and research participants genuinely consenting to undergo treatments and tests and to participate in research.
Henk ten Have   +1 more
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Informed consent

Progress in Transplantation, 2005
In the last half century, informed consent has become a central tenet of all research involving human subjects. However, even after the worldwide adoption of regulations aimed at ensuring the protection of subjects, some abuses continue. The installation of oversight bodies, such as institutional review boards, has prevented the bulk of deliberate ...
Sheldon, Zink   +2 more
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Informed Consent: The Consent Component

Orthopaedic Nursing, 1994
Individuals who participate in treatment or research protocols should perceive that their decision is a free choice and that they are acting of their own accord. However, these persons may feel as if they are being pressured to participate in the protocol being described.
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To consent or not to consent, that is the question

Journal of Data Protection & Privacy, 2019
The General Data Protection Regulation (GDPR) has introduced some significant changes to the processing of data in health and care services. The impact of these changes is now being felt on a wider basis in relation to the question of whether data is processed with consent or not, and even whether we should continue to use the word ‘consent’ when ...
Adam Horton-Tuckett   +1 more
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Broad consent is informed consent

BMJ, 2011
The authors claim that the risks associated with biobanks are minimal and greatly outweighed by the benefits.1 Some people would disagree.2 But even if we could agree about the risks and benefits, different people would weigh them differently: for some, control of personal information is very important and for others less so. For …
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Consenting to the Consent Form

Qualitative Inquiry, 2007
Grounded in the author's dissertation study, this article presents the negotiations of the formal and informal expectations arising out of interpretations of the consent form. These negotiations disrupt the structure of qualitative inquiry and its associated guidelines for academic rigor, trustworthiness, and transferability.
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Informed Consent

Muscle & Nerve, 2001
Abstract All patients have the ethical right of informed consent and refusal that requires physicians, except in emergency treatment, to seek their permission before proceeding with medical care. This right is transferred to a legally authorized surrogate decision maker to exercise on their behalf when patients lose the capacity to make ...
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CONSENT | Treatment Without Consent

2005
As the concept of informed consent to treatment has evolved, so has that of treatment without consent. Although the common law permits treatment without the patient’s explicit agreement in certain circumstances where they are incapacitated in keeping with the doctrine of necessity, the situation has become increasingly complex although statute based ...
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