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- Informed_consent abstract "Informed consent is a process for getting permission before conducting a healthcare intervention on a person. A health care provider may ask a patient to consent to receive therapy before providing it, or a clinical researcher may ask a research participant before enrolling that person into a clinical trial. Informed consent is collected according to guidelines from the fields of medical ethics and research ethics.An informed consent can be said to have been given based upon a clear appreciation and understanding of the facts, implications, and future consequences of an action. In order to give informed consent, the individual concerned must have adequate reasoning faculties and be in possession of all relevant facts at the time consent is given. Impairments to reasoning and judgment which may make it impossible for someone to give informed consent include such factors as basic intellectual or emotional immaturity, high levels of stress such as PTSD or a severe intellectual disability, severe mental illness, intoxication, severe sleep deprivation, Alzheimer's disease, or being in a coma.Some acts can take place because of a lack of informed consent. In cases where an individual is considered unable to give informed consent, another person is generally authorized to give consent on his behalf, e.g., parents or legal guardians of a child (though in this circumstance the child may be required to provide informed assent) and conservators for the mentally ill.In cases where an individual is provided insufficient information to form a reasoned decision, serious ethical issues arise. Such cases in a clinical trial in medical research are anticipated and prevented by an ethics committee or Institutional Review Board.Informed Consent Form Templates can be found on the World Health Organization Website for practical use.".
- Informed_consent wikiPageExternalLink vis-facts.htm.
- Informed_consent wikiPageID "50355".
- Informed_consent wikiPageRevisionID "605611277".
- Informed_consent hasPhotoCollection Informed_consent.
- Informed_consent subject Category:Clinical_research_ethics.
- Informed_consent subject Category:Concepts_in_ethics.
- Informed_consent subject Category:Medical_ethics.
- Informed_consent comment "Informed consent is a process for getting permission before conducting a healthcare intervention on a person. A health care provider may ask a patient to consent to receive therapy before providing it, or a clinical researcher may ask a research participant before enrolling that person into a clinical trial.".
- Informed_consent label "Consenso informato".
- Informed_consent label "Consentement éclairé".
- Informed_consent label "Consentimento informado".
- Informed_consent label "Consentimiento informado".
- Informed_consent label "Informed consent".
- Informed_consent label "Informierte Einwilligung".
- Informed_consent label "Świadoma zgoda na udział w badaniu".
- Informed_consent label "Информированное добровольное согласие".
- Informed_consent label "インフォームド・コンセント".
- Informed_consent label "知情同意".
- Informed_consent sameAs Informovaný_souhlas.
- Informed_consent sameAs Informierte_Einwilligung.
- Informed_consent sameAs Consentimiento_informado.
- Informed_consent sameAs Consentement_éclairé.
- Informed_consent sameAs Consenso_informato.
- Informed_consent sameAs インフォームド・コンセント.
- Informed_consent sameAs 사전동의.
- Informed_consent sameAs Świadoma_zgoda_na_udział_w_badaniu.
- Informed_consent sameAs Consentimento_informado.
- Informed_consent sameAs m.0d9z5.
- Informed_consent sameAs Q764527.
- Informed_consent sameAs Q764527.
- Informed_consent wasDerivedFrom Informed_consent?oldid=605611277.
- Informed_consent isPrimaryTopicOf Informed_consent.