Ethics Flashcards
What does socially sensitive research mean?
Studies where there are potential social consequences or implications for participants or class of individual in research.
What research process did Joan Sieber and Eve Stanley come up with where social consequences occur? (first two steps)
1) The research question: ‘racial differences in IQ’ may be damaging to members of specific groups. Adds scientific credibility to existing prejudices
2) Conduct of research and treatment of participants: ‘if a participant confesses to a crime’ with confidentiality of info being central.
What research process did Joan Sieber and Eve Stanley come up with where social consequences occur? (last two steps)
3) The institutional context: research maybe funded by private organisations which may misunderstand or misuse data. The media may obtain reports and misreport findings (ALL trials campaign):
- drug therapies rely on research to treat mental disorders and most likely are funded by pharmaceutical companies
- selective publication of data = not publish anything that could be harmful to sales
- pre-registration for trials so it can’t be manipulated
-researchers have sponsors who censor data produced
4) Interpretation and application of findings: some research can be applied in unintended ways. IQ tests were created to match individuals to roles but later used to show certain groups inferiority.
Privacy
1) Privacy - skilled researchers may gather unintended info from ppts. E.g. AIDS led to social policies invading people’s private life.
Confidentiality
2) confidentiality: ppts may not share info if confidentiality is breached. Future research could be compromised.
Valid methodology
3) Valid methodology: where poor methodology or invalid results are found. Scientists are aware of this problem, but public may not be aware of this issue and base social policy in a detrimental way.
Deception
Research can create false sterotypes affecting performance.
Equitable treatment
ALL ppts must be treated equally. Essential resources should be available to everyone.
Informed consent
Ppts may not always understand what is involved.
Scientific freedom
Scientists have the duty to engage in research while being obliged to not harm ppts and institutions.
Ownership of Data
Determining ownership is difficult as they include sponsorship: commercial/university. Public access to data is important.
Values
Psychologists differ in their approaches (IV’s and N) and objectiveness. A clash within such values between scientists and recipients of research give rise to sensitive issues.
Risk/benefit ratio
Risks or costs should be minimised but there are problems that arise in determining these risks and benefits.