Midterm 2 (4, 7, 12, 13) Flashcards
What are the 2 basic categories of ethical responsibility
- Responsibility towards the participants/subjects (ensure their welfare/dignity)
- Responsibility towards the discipline of science to be accurate and honest in the diffusion of results
What are research ethics?
Concerns the responsibility of researchers to be honest/respectful to all individuals who are affected by their research studies or reports
What are ethical principles?
Dictate how studies should be conducted from beginning to end in an ethical way
What are the 3 principles of the Belmont report? Also the 3 politics of the Tri-Council Policy Statement (prevalent in Canada)
- Principle of Respect for persons (autonomy): Individuals should be able to consent to participate in studies. Those who cant give consent should be protected
- Principle of Beneficence: Researchers have to minimize harm/risks, while maximizing possible benefits
- Principle of Justice: Fair and non exploitative procedures for the selection of participants (represent the pop who will benefit from this study)
What is the principle of no harm (APA guideline)?
The researcher has to protect participants from (psychological/physiological) harm, all possible harm has to be identified, minimized and justified. Participants must be made aware of risks and offered post-experiment assistance.
What is clinical equipoise?
Clinicians have to give best possible treatment to their patients. In studies sometimes there are treatments perceived to be better than others (ex: placebo vs actual treatment). The No Harm principle is violated
• Solution: compare only equally preferred treatments (or honest uncertainty about which is best)
What is the principle of informed consent (APA guideline)?
Human participants should be given complete info about the study/their role in it before participating (in broad terms, not to affect the participant’s behaviour)
What is one of the possible problems regarding blind studies and informed consent?
Sometimes we cannot say everything to the participants first hand. The solution is to explain what will be done but not explain why (reveal enough for the participant to be comfortable but not too much to influence their behaviour)
What is assent?
Consent obtained directly from the participants
What is consent?
Obtained from the official guardians of the people who cannot consent to the study
What is passive deception (omission)?
Concealing the true nature of the study
What is active deception (comission)?
Deliberately present false info (confederates)
Ex: not telling participants that their memory will be tested until we test their memory
What is the type of info we cannot conceal from the participants?
Possible harm
What is debriefing? Why is it required
Because the principle of informed consent is being violated with deception, researchers must debrief the participants by telling the participants what was the study about, counteracting or minimizing any negative effects of the study, explaining nature of study, allowing any questions (not always effective)
Can we inform the participants that there will be deception?
Yes, if we use a placebo group
What is the principle of confidentiality (APA guideline)?
All info collected about participants might be deemed personal (attitudes/opinions, measures of performance, demographics), and have to be protected by confidentiality guidelines (= protection of data)
What is anonymity?
Practice of ensuring that an individual’s name/identity is not directly associated with the info/measurements obtained (= protection of identity)
What are the 2 strategies that might be used for confidentiality?
- No names/identification appears on records of data (when participants do not have to be linked with their results)
- Coding system to link participants with data (when necessary) (pseudonyms, code names)
When does research that relies exclusively on publicly available info does not require consent?
- Info is legally accessible to the public and appropriately protected by law
- The info is publicly accessible and there is no expectation of privacy
When is consent not required for the observation of people in public spaces?
- There is no intervention staged by the researchers
- There is no reasonable expectation of privacy (people know that they are in a public space)
- The dissemination of research results would not allow the identification of specific individuals
What are the 2 major problems on collecting data on internet?
• Expectation of privacy
• Persistence and traceability of quotes/info
Internet users do not expect to be subjects; they are most likely to perceive information collection as invading privacy
How can we protect anonym,ity when we took quotes from Internet?
- Do not identify name/provide website address
- Anonymise and paraphrase quotations + use search engines to ensure that they are not traceable
- Use composite instead of direct quotes
What are 3 reasons to choose animal subjects in research?
- To understand animals for their own sake
- To understand humans
- To conduct research that is impossible to conduct using human participants
What are the 2 cases in which animal research is acceptable?
- Only acceptable if it contributes to the understanding of fundamental biological principles or
- To the development of knowledge that can reasonably expected to benefit animals or humans