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PubMed · 8107003

The research process: informed consent.

Abstract

Informed consent is a vital part of the research proposal and study. Informed consent is based on principles of autonomy ie, individuals have a right to full disclosure of information in order to make an informed decision and to assume responsibility for the consequences of their decision. Informed consent also contains a legal element whereby failure to obtain it is considered negligence and/or battery. Conducting studies when patients are medicated, ill, or very young or very old require special steps to verify that subjects are fully informed. It is important that PACU nurses pay particular attention to the informed consent process when planning and conducting research studies.

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BibTeXRIS

S Summers. 1993. The research process: informed consent.. https://pubmed.ncbi.nlm.nih.gov/8107003/

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The wording of the informed consent in gynecology.

In many western States medical activity is characterized by legal difficulties regarding the patients' consent. In this paper we have confronted the medical and legal problems connected to the wording of the informed consent in diagnostic and therapeutic practice in gynecology and obstetrics. In this area the role of Scientific Societies seems ever more important in that they could carry-out an important task by having the possibility of acquiring and coordinating the maximum amount of knowledge in both the specialistic medical field and the judiciary field. Here, we discuss the various aspects of the preparation of appropriate forms for correct patient information and the valid acquisition of the patient's consent for medical records.

Consent Forms