Ch2: Research Ethics Flashcards
What is the importance of IRB (Institutional Review Board)?
- To evaluate proposed studies before they are conducted
- To Ensure the safety of participants
- To Safeguard the rights of the subjects through informed consent
What protects human participants?
Federal law
Science is immoral.
False, it’s amoral, neither moral nor immoral, facts discovered through science just happen to exist.
However, it becomes unethical depending on the procedures it was undertaken.
The foremost concern in recruiting and using subjects.
Treating them ethically and responsibly
The search for knowledge is more important than the well-being of participants.
False, research that is harmful to the participants is undesirable even if they increase wisdom.
The IRB is composed of__
- Laypeople
- Researchers
- Scientists
What is the primary duty of a review board?
To ensure the safety of research participants is adequately protected.
What is risk/benefit analysis?
The process of IRB to determine if any risks to individuals are outweighed by potential benefits or the importance of the knowledge to be gained.
(Weighing process of risks and benefits)
Enumerate the 3 important reasons why poorly design research can be unethical.
- time will be taken from potentially more beneficial educational experiences.
- It can lead to inaccurate and unwarranted conclusions that may be damaging to society
- Resources (time and money) are finite
It means that the subject agrees to participate after having been fully informed about the nature of the study.
informed consent
Consent must be given freely.
True
What are the aspects of informed consent?
- Consent must be given freely
- Subjects must be free to drop out of the experiment at any time
- Subjects must be given a full explanation of the procedures and are given answers to questions about it
- Risks must be explained in advance
- Subjects must be assured of confidentiality
- Consent should be obtained in writing and subject must receive a copy to keep
What is an assent?
It is an informed consent for minors or cognitively impaired subjects
What are the relevant information that should be disclosed in consent?
- Nature of experiment
- Overview of procedures
- Length or how long will it take
- Potential risks and benefits
- What subjects are required to do
What is the overall purpose of consent?
It is to give subjects enough info about the experiment so that they can make an informed decision on whether or not to participate.
It is the government policy statement on research involving human subjects
Belmont Report