Ch 7: Ethics Flashcards
In response to human rights violations, various ____ of ____ have been developed.
Codes of Ethics
What is the code of ethics in the United States adopted by the National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research?
Belmont Report
What are the three broad principles articulated in the Belmont Report?
beneficence, respect for human dignity, and justice
What is beneficence?
- imposes a duty on researchers to minimize harm and maximize benefits
- harm can be considered physical, emotional, social, or financial
Obligation to avoid, prevent, and minimize harm
nonmaleficence
What are some principles under beneficence?
- the right to freedom from harm and discomfort
2. the right to protection from exploitation
What are some principles under respect for human dignity?
- the right to self-determination (prospective participants can voluntarily decide whether to take part or not without risk of prejudicial treatment)
- The right to full disclosure (researcher has fully described the nature of the study, the person’s right to refuse participation, the researchers responsibilities, and likely risks and benefits)
collection of data without participant’s knowledge and consent; researchers obtain data through concealed methods like hidden equipment or observing while pretending to be engaged in something else
covert data collection
Deliberately withholding information about the study or providing participants with false information
deception
What are the principles under Justice?
- The right to fair treatment (participant selection is based on study requirements and not on a group’s vulnerability; researchers can’t neglect nor discriminate against individuals or groups who may benefit from research (ex. women and minorities); researchers must treat people who decline to participate or who withdraw in a nonprejudicial manner)
- The right to privacy
Assessment designed to examine whether the benefits of participating in a study are in line with costs, be they financial, physical, emotional, or social
risk-benefit assessment
Risks no greater than those ordinarily encountered in daily life or during routine tests or procedures
minimal risk
Participants have adequate information about the research, comprehend that information, and have the ability to consent to or decline participation voluntarily
informed consent
What 15 pieces of information have to be communicated to participants for informed consent?
- participant status
- study goals
- type of data
- procedures
- nature of the commitment
- sponsorship
- participant selection
- potential risks
- potential benefits
- alternatives
- compensation
- confidentiality pledge
- voluntary consent
- right to withdraw and withhold information
- contact information
Most secure means of protecting confidentiality- occurs when researcher cannot link participants to their data
anonymity