Chapter 7 Flashcards
Informed Consent
A process that involves informing a participant about research and obtaining consent to participate in it
Nuremberg Code
Laid the groundwork for many of the current ethical standards for psychological and medical research
Declaration of Helsinki
Adopted by the World Medical Association. Addresses ethical codes that apply to medical research, and research in the social science.
Belmont Report
Issued in 1979 and further delineated ethical research practice with human participants
Respect for Persons
Two components
- ) Research participants must be treated as individuals who are capable of making their own decisions
- ) Persons with diminished autonomy or capacity deserve protection
Beneficence
Do no harm to participants and to maximize benefits while minimizing harm
Justice
States that both the researcher and the participant should share costs and potential benefits
Ethical Principles of Psychologists and Code of Conduct 2002
Comprehensive document specifying the ethical responsibilities of psychologists and researchers
Institutional Review Board (IRB)
Board that reviews research for ethical concerns
Institutional Animal Care and Use Committee (IACUC)
The committee that approves research using animals
Office of Research Integrity (ORI)
An office within the U.S. Department of Health and Human Services that oversees the integrity of the research process