Results 11 to 20 of about 3,231,462 (251)

Ensuring that informed consent is really an informed consent: Role of videography

Perspectives in Clinical Research, 2014
The voluntary consent of a subject participating in research is fundamental to the principle of autonomy. This consent must be free from any coercion, intimidation, falsehood, physical, psychological, or economic pressure.
Ravindra B Ghooi
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The Potential Perils of Informed Consent

McGill Journal of Medicine, 2020
N ...
Elizabeth F. Loftus, James F. Fries
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Preoperative Informed Consent: Is It Truly Informed? [PDF]

Iranian Journal of Public Health, 2012
Background: Pre-operative informed consent is an important aspect of surgery, yet there has been no formal training regarding it in Pakistan. This study was done to assess the preoperative informed consent practice.
SMN Husnain, Z Masood, M Farhan, M Jawaid   +3 more
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How informed are you about informed consent?

Indian Journal of Vascular and Endovascular Surgery, 2019
The past decade has seen a rise in the awareness of patients, and their attendants have about their disease, options for treatment and their legal rights, thanks to easy access to the Internet, however accurate it may be. Surgeons need to be aware of the
Edwin Stephen
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Context-sensitive Dialogues

Etikk i Praksis: Nordic Journal of Applied Ethics
This article reflects on the central themes of Vilhjálmur Árnason's work, particularly his focus on contextualized morality and dialogical ethics.
Vilhjalmur Arnason
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Informed consent and HIV

Southern African Journal of HIV Medicine, 2001
No abstract available.
Steve Andrews
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Improving assent in health research: a rapid systematic review

BMC Medical Research Methodology, 2020
Background Enrolment in a research study requires the participant’s informed consent. In the case of minors, informed consent of the respective legal guardian is obtained in conjunction with informed assent of the underage p articipant.
Dominik Soll, Maria Magdalena Guraiib, Nigel Campbell Rollins, Andreas Alois Reis   +3 more
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Quality of informed consent in clinical trials

Journal of Pre-Clinical and Clinical Research, 2020
Introduction and objectives Obtaining consent prior to any medical intervention is currently a necessity, the omission of which may lead to litigation. Years of analyses have resulted in strict policies as to what should the patient be informed about and
Anna Zagaja
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Informed consent in clinical trials

South African Journal of Bioethics and Law, 2022
Background. Informed consent (IC) is not only a regulatory but also an ethical requirement to participate in any clinical trial. It is essential to determine that research participants understand what they consent to.
G P Kovane, V C Nikoderm, O Khondowe
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False Hopes, Informed Consent

Voices in Bioethics, 2013
In America, with our closely held values of optimism and perseverance, we are very often loath to confront death and dying; cancer patients are told to fight, to hold on to a positive attitude, to nurture faith and hope.
Jennifer Cable
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