BPS: ethical Principles & Guidlines Flashcards

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1
Q

Why is the bps?

A

Association that supports psychologists & regulates the profession.

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2
Q

Why are each guideline in place?

A

Ensure participants are protected during research but to also ensure participants will take part in studies.

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3
Q

Ethical principle- respect- define respect in this case?

A

Being willing to explain the ethics of any study/practise & maintaining the dignity of others particularly in regards to culture, role and individual differences.

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4
Q

Define ethical principle.

A

Body which releases codes to guide psychologists.

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5
Q

Ethical principle- respect- what is the link to ethical guidelines?

A

Includes informed consent, confidentiality, privacy and right to withdraw.

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6
Q

What is the difference between privacy & confidentiality?

A

Privacy: a right to.
Confidentiality: should be respected.

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7
Q

What is a participants view on privacy?

A

Everyone has an expectation.
Have a right to decide who knows and who doesn’t.

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8
Q

What is a researches view on privacy and give an example?

A

Might be difficult.
Eg: conducting an observational study- observers don’t want them to know as it can affect their behaviour.

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9
Q

What is a participants view on confidentiality and give an example?

A

Data protection app- legal right to have their personal information protected.
Eg: no one should be able to connect what a participant does in a study to their personal details.

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10
Q

Informed consent: what does it look like?

A

Participants must be given comprehensive information concerning the nature & purpose of a study & their role in it.

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11
Q

Informed consent: what is a participants view on it?

A

Wish to know what they are letting themselves in for if they agree.

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12
Q

Informed consent: what is it necessary for?

A

In order to make informed decisions about whether to participate in a study.

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13
Q

Informed consent: how might vulnerable individuals feel?

A

Eg: children can’t give informed consent and may not be happy that a parent/ guardian gave it on their behalf.

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14
Q

Informed consent: what is a researchers view on it and give an example?

A

Providing comprehensive information may reduce meaningfulness of the research.
Eg: information could reveal study’s aims and could affect participants behaviour.

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15
Q

Deception: when does it happen and give an example?

A

When a participants is not told the true aims of a study or is deliberately misled in some way.
Eg: participants may be given some details about what they will be required to do but other information that may affect their behaviour will be withheld.

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16
Q

Deception: what is a scenario in which this would be used?

A

Might be told that they will have to answer a question bout a certain situation but not told5at their obedience is being assessed.

17
Q

Deception: what is a participants view on it?

A

Issue because it prevents participants being able to give truly informed consent as they don’t have all the necessary information to make that decision.

18
Q

Deception: what is a researchers view on it?

A

Some can be relatively harmless and can be compensatied for by an adequate debriefing.

19
Q

Deception: what is an example of where this would happen and what the effect be?

A

Eg: memory experiment participant may not be told that at the end they will be asked to rate faces for attractiveness instead of recall.
Doesn’t cause significant embarrassment or harm.

20
Q

Deception: what is the fine line between deception and give an example?

A

Withholding knowledge and telling participants a lie.
Telling them the study is bout something completely different to the true aims.

21
Q

Right to withdraw: what does it mean?

A

Participants have the right to know they can freely decide not to continue participation in a study at any time.

22
Q

Right to withdraw: what is a participants view?

A

Important if some information was withheld at the beginning of the study or if they didn’t really understand what might be involved.

23
Q

Right to withdraw: what may act as a barrier and give an example?

A

My feel they shouldn’t withdraw because it will spoil the study.
Eg: in some studies participants are paid or rewarded in some way so many may not feel able to withdraw.

24
Q

Right to withdraw: what is a researchers view on it?

A

Loss of participants may bias the study’s findings because the participants who leave e more confident or more intelligent.

25
Q

Right to withdraw: what does it ensure?

A

Feel comfortable at all times.

26
Q

Right to withdraw: what else does it ensure in terms of what is allowed to be recalled?

A

Right to withdraw data at the end of the study if they were unhappy about their participation.

27
Q

Protection/ risk from harm: what does harm include and give examples?

A

any negative physical effects, risk to participants values, beliefs, relationships, status, privacy.
Eg: injury, asking to drink alcohol, smoke, psychological effects (anxiety, humiliation or embarrassment.)

28
Q

Protection/ risk from harm: what is the participants view?

A

Have a no desire to be harmed, expect to be in the same state before and after.

29
Q

Protection/ risk from harm: what is reasonable though?

A

To expose individuals to risks equivalent to what would be experienced in their everyday life.

30
Q

Protection/ risk from harm: what is a researchers view?

A

May not be possible to estimate all possible negative effects before conducting a study.

31
Q

What is an ethical issue?

A

Conflict between what the researcher want and the rights of the participant.
What is acceptable.

32
Q

What are the different ways of dealing with ethical issues?

A

Risk assessment and management, consent and debriefing and research ethics committee.