Giving participants info about the study (aim, procedure etc.)
so they can make an informed decision
Can tell aims at end of study if it would ruin research
Participants are told they can leave any time- right to withdraw
Deception
Participants should not be misled or lied to about the aims of the study without justification
Acceptable to mildlydeceive (withhold some info)
Major deception can be acceptable only if the benefitsoutweigh the ethical costs of research
Protection from Harm
Participants should not be at risk
psychological/physical health should be protected at all times
Stress and embarrassment are included in this
Reminding participants they can leave at any time
Confidentiality
Personal data and identity should be protected and respected- kept anonymous
Privacy
Participants should have the right to control their data and how it is used
This is not always possible – field experiments.
It is acceptable to observe people in public places but a public place can be quite private e.g a conversation in a restaurant
Dealing with Informed Consent
Researchers should produce a letter explaining what the study will involve – consent form.
Participants should then sign consent form
U16s – parents give consent
If it isn't possible at the start, they sign a form at the end of the study- RETROSPECTIVE CIONSENT
If consent can't be obtained, researcher must have very good reason.
Dealing with Deception
Can decide to withdraw during study and right to withdraw data at the end
Participants should be debriefed at the end to explain the trueaims and reduce any distress
Dealing with Protection from Harm
If participants feel any discomfort from completing the study, psychologist is responsible for "fixing" it.
May be offered counselling
Told they can withdraw at any time during the study
FULL debrief
Dealing with Privacy/Confidentiality
Keep datasafe
Participants should remain anonymous e.g. can be reffered to by a number or initials
Can also decide to keep location of study anonymous
What are ethical issues?
An ethical issue is when there is a conflict between the rights of participants to remain safe and protected and the need for researchers to gain valuable data
The well being of participants must be protected at all times
The BPS guidelines
a code of conduct that every professional psychologist in the UK must follow in order to deal with ethical issues in their research