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Informed consent
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display title: Informed consent
has best practice: The idea of written informed consent is not new. It first appeared in the early 20th century in Walter Reed’s research of yellow fever.'"`UNIQ--ref-00000002-QINU`"' The development of human rights after the second World War brought to life numerous declarations and rules (e.g., the Nuremberg Code) regarding human experimentation.'"`UNIQ--ref-00000003-QINU`"' In order for informed consent to be valid, four conditions need to be met'"`UNIQ--ref-00000004-QINU`"': *Voluntariness: subjects should not be coerced. This could be a tricky condition sometimes, especially when subjects have no alternative choice (e.g., when a terminally ill patient is offered to join an experiment that might save their life) *Capacity: subjects should have the capacity to understand and judge provided information. This could become a thorny issue when dealin with vulnerable subjects (e.g., children) or patients with mental problems (e.g., those suffering from illnesses such as dimensia) *Information: subjects should be provided with adequate amount of information. These may include methodology, process, duration of the experiment, but also research goals, beneficiaries, data retention schedule, others uses of extracted data (e.g., publication of research articles, use of material in tangent projects, etc.). *Comprehension: subjects should understand the provided information. Relevant considerations include using straightforward language that is understandable for the least advantaged members of the target group, and avoding the use of scientific jargon. Before accepting a manuscript for publication, editors should make sure authors have all the necessary research ethics permissions and signed informed consent forms from all participants. '"`UNIQ--references-00000005-QINU`"'
has good practice and misconduct: Informed consent
has good practice and misconduct: Vulnerable and non-competent subjects
has virtue and value: Respect
important because: In order to maintain high standards of research ethics, personal dignity and autonomy must be respected. To achieve this, before conducting research, researchers have to seek informed consent from participants.
important for: Researcher
important for: Senior Researcher
important for: Doctoral Student
important for: Early Career Researcher
important for: Research Participant
is about: Informed consent is a process of acquiring permission from potential participants, before conducting some sort of medical intervention, collection of personal data or enrollment in a study.'"`UNIQ--ref-00000000-QINU`"' '"`UNIQ--references-00000001-QINU`"'
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theme type: Good Practices
title: Informed consent
wiki page creation date: 2019-12-06T15:42:19Z
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wiki page modification date: 2026-03-03T13:42:37Z
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Consent and Assent for Research on Children
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Informed consent in psychiatry
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wiki page sort key: Display Title: Informed consentInformed consent in psychiatry

A Review of the Impact of the TeGenero Trial on the Design, Conduct, and Ethics of FIM Trials
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Anonymity Revisited
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Assessing the educational literature in the responsible conduct of research for core content.
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Banked Samples and HD Testing
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Consent and assent in research on children
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Data Practices, Data Management and FAIR Principles: An Educational Scenario by the EnTIRE project
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Ethics Framework and Guidelines for Participatory Processes in the Activities of Research Funding Organizations
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Ethics Framework and Guidelines for Participatory Processes in the Activities of Research Funding Organizations
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History, Ethics and the Presidential Commission on Research in Guatemala
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Institutional Pathology and the Death of a Mentally Ill Young Man
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Jesse's Intent
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Protection of Research Participants
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Publishing complications and patient safety
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Safeguards, Data-sharing and the Disclosure of Sensitive Results: An Educational Scenario by the EnTIRE project
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The Art and Politics of Covert Research: Doing ‘Situated Ethics’ in the Field
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The Nuremberg Code
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The Olivieri Debacle: Where Were the Heroes of Bioethics?
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The Saga of Korean Women Who Provided Eggs for Embryonic Stem Cell Research
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The Unfortunate Experiment
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The role of moral philosophy in the divide between science and non-science
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Unlicensed usage of medical devices on patients: a case of accusations
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When Sociologists Deceive Their Subjects
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Withholding Study Purpose
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Consent and assent for research on children
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wiki page sort key: Display Title: ConfidentialityConsent and assent for research on children

Conducting research in high risk locations
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Confidentiality
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Incidental research findings
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Informed assent
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Internet Research Ethics
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Privacy in research
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Research with children
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Vulnerable and non-competent subjects in clinical trials
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Consent for publication (Participant)
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Ignoring substantial safety risks of studies
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Is there an overall theme which already addresses some relevant points?
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Related Themes
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Related To Object
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