Week 2 Flashcards
Protection of participants in a study such that even the researcher can- not link individuals with the information provided.
Anonymity
A fundamental ethical principle that seeks to prevent harm and exploitation of, and maximize benefits for, study participants.
Beneficiance
A written agreement signed by a study participant and a researcher concerning the terms and conditions of voluntary participation in a study.
consent form
In a qualitative study, an ongoing, transactional process of negotiating consent with study participants, allowing them to play a collaborative role in the decision making regarding their continued participation
process consent
Protection of participants in a study such that individual identities are not linked to information provided and are never publicly divulged.
confidentiality
The relative costs and benefits, to an individual subject and to society at large, of participation in a study; also, the relative costs and benefits of implementing an innovation.
risk/benefit assessment
A group established within Canadian universities, hospitals, and other institutions where research is conducted to ensure that ethical principles are applied to research involving human subjects
Research Ethics Board (REB)
was adopted in 1964 by the World Medical Assembly and most recently revised in 2000; is a set of ethical principles regarding human experimentation developed for the medical community
Declaration of Helsinki
Ex. Children, mentally or emotionally disabled people, and others who are unable to understand information or appreciate the consequences of participation.
vulnerable person
The communication of complete information to potential study participants about the nature of the study, the right to refuse participation, and the likely risks and benefits that would be incurred.
full disclosure
means that prospective participants have the right to decide voluntarily whether to participate in a study, without the risk of incurring adverse consequences. Also means that participants have the right to ask questions, to refuse to give information, and to withdraw from the study.
self-determination
Consent to participate in a study that a researcher assumes has been given based on certain actions of the participant (such as returning a completed questionnaire).
implied consent
An ethical principle that requires researchers to obtain the voluntary participation of subjects, after informing them of possible risks and benefits.
informed consent
is a set of research ethics principles for human experimentation developed in 1949 after the Nazi atrocities were made public
Nuremberg code
guidelines used to protect human subjects in all types of research. Articulates 8 guiding ethical principles on which standards of ethical conduct in research are based.
Tri-Council Policy
includes the principles of beneficence, respect for human dignity and justice.
Belmont Report
Special groups of people whose rights in research studies need special protection because of their inability to provide meaningful informed consent or because their circumstances place them at higher-than-average risk of adverse effects
vulnerable group
The fundamental ethical principles established by a discipline or institution to guide researchers’ conduct in research with human (or animal) subjects.
code of ethics