Informed consent from behaviourally disturbed patients.
2002
Jitschak Storosum, and
Barbara van Zwieten, and
Lieuwe de Haan
UI
MeSH Term
Description
Entries
D007258
Informed Consent
Voluntary authorization, by a patient or research subject, with full comprehension of the risks involved, for diagnostic or investigative procedures, and for medical and surgical treatment.
Consent, Informed
D002986
Clinical Trials as Topic
Works about pre-planned studies of the safety, efficacy, or optimum dosage schedule (if appropriate) of one or more diagnostic, therapeutic, or prophylactic drugs, devices, or techniques selected according to predetermined criteria of eligibility and observed for predefined evidence of favorable and unfavorable effects. This concept includes clinical trials conducted both in the U.S. and in other countries.
Clinical Trial as Topic
D004992
Ethics, Medical
The principles of professional conduct concerning the rights and duties of the physician, relations with patients and fellow practitioners, as well as actions of the physician in patient care and interpersonal relations with patient families.
Medical Ethics
D006801
Humans
Members of the species Homo sapiens.
Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D016743
Mental Competency
The ability to understand the nature and effect of the act in which the individual is engaged. (From Black's Law Dictionary, 6th ed).
The moral obligations governing the conduct of research. Used for discussions of research ethics as a general topic.
Research Ethics
D035841
Behavioral Research
Research that involves the application of the behavioral and social sciences to the study of the actions or reactions of persons or animals in response to external or internal stimuli. (from American Heritage Dictionary, 4th ed)
Research, Behavioral
Related Publications
Jitschak Storosum, and
Barbara van Zwieten, and
Lieuwe de Haan