Children’s views on research without prior consent in emergency situations: a UK qualitative study

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منابع مشابه

Research in emergency situations: with or without relatives consent.

Patients in emergency situations with impaired consciousness are unable to give informed consent to participate in clinical trials. In this situation, some ethics committees ask that consent is obtained from a relative or a legal representative. Others however, waive the need for informed consent and allow the doctor in charge to take responsibility for entering such patients. This study used d...

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How parents and practitioners experience research without prior consent (deferred consent) for emergency research involving children with life threatening conditions: a mixed method study

OBJECTIVE Alternatives to prospective informed consent to enable children with life-threatening conditions to be entered into trials of emergency treatments are needed. Across Europe, a process called deferred consent has been developed as an alternative. Little is known about the views and experiences of those with first-hand experience of this controversial consent process. To inform how cons...

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Qualitative evaluation of a deferred consent process in paediatric emergency research: a PREDICT study

BACKGROUND A challenge of conducting research in critically ill children is that the therapeutic window for the intervention may be too short to seek informed consent prior to enrolment. In specific circumstances, most international ethical guidelines allow for children to be enrolled in research with informed consent obtained later, termed deferred consent (DC) or retrospective consent. There ...

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Clinical research without consent in adults in the emergency setting: a review of patient and public views

BACKGROUND In emergency research, obtaining informed consent can be problematic. Research to develop and improve treatments for patients admitted to hospital with life-threatening and debilitating conditions is much needed yet the issue of research without consent (RWC) raises concerns about unethical practices and the loss of individual autonomy. Consistent with the policy and practice turn to...

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A qualitative study of participants’ views on re-consent in a longitudinal biobank

BACKGROUND Biomedical research increasingly relies on long-term studies involving use and re-use of biological samples and data stored in large repositories or "biobanks" over lengthy periods, often raising questions about whether and when a re-consenting process should be activated. We sought to investigate the views on re-consent of participants in a longitudinal biobank. METHODS We conduct...

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ژورنال

عنوان ژورنال: BMJ Open

سال: 2018

ISSN: 2044-6055,2044-6055

DOI: 10.1136/bmjopen-2018-022894