Main Ethical Principles • Informed consent/withdrawal
• Deception
• Protection of participants
from harm
• Privacy & Confidentiality
Informed consent Participants must be given comprehensive information
concerning the nature and purpose of a study and their
role in it.
• Aim of research
• The procedures
• Their rights to withdraw
• What their data will be used for
• From the researchers point of view, asking for informed
consent may make the study meaningful.
Deception Deception mean deliberately misleading or withholding
information from participants at any stage of the
investigation.
Researchers should avoid deceiving participants where
possible. However, the BPS recognises that there is a
difference between falsely informing participants about the
aim of the study and withholding some information about
the aims of the study.
For example, in our energy study it would probably be acceptable not to tell
participants that there is another group drinking a different substance, as
knowing this may affect their behaviour.
Protection from harm Investigators have a primary importance to protect
participants from any physical/ mental harm during
the investigation.
• Participants should not be exposed to harm any
greater than would normally occur in everyday life
• Physical and psychological harm (e.g. stress, damage
to self image, under pressure)
• Participants should leave (rights to withdraw) the
study unchanged from how they entered it
(debriefing)
Privacy and confidentiality
All data should be confidential, all PPs should be anonymous and unidentifiable. (e.g. through use of numbers; not recording
names etc.)
• Confidentiality refer to our right, protected under the Data
Protection Act, to have any personal data protected.
• The rights to privacy extends to the area where the study took
place, such as institutions
• PPs’ right to privacy must be respected since invasions of privacy
may affect well-being and raise confidentiality issues
What is the primary role of ethics committees in research?
To make judgments about the costs and benefits involved in research
when a conflict occurs between participants rights and researchers aim and need to gain valuable findings
British psychological society BPS
The society that governs psychology in Britain and controls the profession. upholds high standards of professionalism promoting ethical behaviours
Informed consent
an ethical principle that research participants be told enough to enable them to choose whether they wish to participate resreachers must tell participants all aspects of the research that are likely to influence their willingness to take part in the study participants must be given the right to withdraw and fully understand the aims of the research and procedure special care is needed when dealing with chilldren and vulnerable adults the purpose of the study should be explained to them in the language they understand
Deception
misleading participants about the true purpose of a study or the events that will actually transpire with holding information from participants at any stage of the experiment researchers should avoid deceiving participants
Protection from harm
Investigators have a primary responsibility to protect participants from physical and mental
harm during the investigation.
- The risk of harm must be no greater than in ordinary life.
Privacy and confidentially
Protect the privacy of the participant, generally by keeping all responses participants should be anonymous
Ethics committee
is the body that is responsible for ensuring that medical experimentation and Human subject research is done in a ethical manner
Cost benefit analysis
costs are negative consequences on a research this may have a damaging effect on the partcipant or the reputation of psychology
Dealing with informed consent
participants should be issued with consent letter or form detailing all info that might affect their decision to participate -parental consent if under 16
Dealing with deception and protection from harm
Debriefing = made aware of true aims after study and any details not supplied during like other conditions, must be given right to withhold data (important for retrospective consent), should be reassure behaviour is normal and offer counselling
Dealing with confidentially and privacy
Dealing with confidentiality can be done by keeping the participant anonymous and keeping their personal data protected when participants are debriefed they must be reminded that their data is protected Researchers may give retrospective consent asking consent after the research
And presumptive consent asking before the research