Research Methods- Ethics Flashcards
Ethics/ ethical guidelines:
Practicing psychologists are expected to design and conduct research that follows a set of guidelines published by the BPS (British psychological society) in the UK and APA (American psychological association) in the USA.
BPS
British psychological society
The role of the British Psychological Society’s code of ethics:
“designed to inform and assist our members in the practical and professional application of psychology, from research and teaching to clinical practice.” - BPS
BPS’s Ethical research ‘first principles’
Respect for the autonomy, privacy and dignity of individuals, groups and
communities.
Scientific integrity.
Social responsibility.
Maximising benefit and minimising harm.
Legality?
The guidelines are not “rules or laws”, but a set of professional advice that requires psychologists to exercise professional judgement in complex research situations.
Informed consent:
Consent is not valid if participants are not informed of what they are agreeing to. So before the research participants should be made aware of the aims, and consequences of taking part in research (e.g. risk of harm, potential benefits of research). Consent may be gained from a parent or guardian if the participant is unable to give informed consent themselves (e.g. children, mentally incapable).
Informed consent linked to…
Informed consent is linked to the principle that we shouldn’t deceive participants.
However deception is part of many studies, used to avoid demand characteristics.
Right to withdraw
Participants (as part of giving informed consent) should be told they can withdraw from the study at any stage with no adverse consequences (e.g. not being paid for their time). This incudes withdrawing data collected from them.
Protection from harm:
The researcher is responsible for designing research that does not risk the psychological well-being, physical health, personal values and dignity of the participants.
Confidentiality
Participants’ personal data should be kept securely by the researcher, and not shared. When the research is published it should not include the identity of participants or information that could reveal the identity of participants. However, there are exceptions, such as finding out the participant or others are in danger.
Debriefing
After the data collection is completed the researcher should offer a debriefing, this would reveal any information withheld, such as the existence of other groups (e.g. they received a placebo while the other group received therapy). The researcher can also check for any psychological or physical harm and offer assistance.
Ethical guidelines
5
Informed consent/ deception
Right to withdraw
Protection from harm
Confidentiality
Debriefing
Milgrams study
5
Revealing the true aims of a study when asking for informed consent can lead to…
demand characteristics, participants altering their behaviour to match what they think the researcher wants to find, and this reduces the internal validity of the research. The researcher can avoid this by using an alternative to informed consent.
Prior general consent:
Participants agree to a long list of potential features of a research study, not knowing which aspects will be part of the study they are in.