These arise when conflict exists between the rights of ppts in research and the goals of the research to produce valid data
Define the ‘BPS code of ethics‘
A quasi-legal document produced by the British Psychological Society that instructs psychologists in the UK about what behaviour is/is not acceptable when dealing with ppts
What are the 4 major principles of the ‘BPS code of ethics’
1.Respect
2.Competence
3.Responsibility
4.Integrity
Define ‘informed consent’
Involves making ppts aware of the aims of research, the procedure, their rights and what the data will be used for then making a decision on whether to take part or not
How to deal with ‘informed consent‘
1.Consent letter
2.Presumptive consent = ask a similar group
3.Prior general consent = give permission to numerous different studies (inc. one that involves deception)
4.Retrospective consent = asked post study
Define ‘deception’
Means deliberately misleading or withholding information from ppts
How to deal with ‘deception’
Give full debrief
Define ‘protection from harm‘
Ppts should not be at any more risk as they would be in their daily lives (physically and psychologically)
How to deal with ‘protection from harm’
Counselling
Define ‘privacy‘
Refers to ppts having the right to control info about them
Define ’confidentiality‘
Refers to our right by law (Data Protection Act) any personal data should be protected
How to deal with ‘privacy and confidentiality‘
1.Maintain anonymity (use fake names)
2.Mention in briefing/debriefing that personal data will not be shared