ethical issues Flashcards

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1
Q

BPS

A

British Pyschological Society - nationally recognised professional body who have developed a set of ethical guidelines to ensure the protection of participants in pyschological research

all psychological research in the UK has to be approved by BPS ethics committees before being carried out. If psychologists break this ethical code, they can be struck off the national register of practicing psychologists, making it difficult for them to continue working in the UK

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2
Q

Physical harm

A

participants have the right to not experience any harm in research

includes any physical pain or discomfort

a study can be considered not to have caused lasting psychological or physical harm if participants leave in a frame of mind that is at least as sound as when they entered (Aronson, 1988)

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3
Q

physical and psychological harm BPS guidelines

A

researchers should protect participants from harm during any study

the risk of harm should be no greater than the risks experienced in ordinary line

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4
Q

dealing with harm

A

at the end of the study, participants should receive a full debriefing in which they are informed of the full details of the research, including discussion of their harm

a debriefing should ensure that participants have overcome their harm, leaving in a “frame of mind that is at least as sound as when they entered” Aronsonn, 1988

if not, they have the right to withdraw their data from the investigation

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5
Q

psychological harm

A

participants have the right not to experience harm in research

psychological harm includes any level of emotional distress, embarassment or the loss of self-esteem

a study can be considered not to have caused lasting psychological or physical harm if participants leave in a “frame of mind that is at least as sound as when they entered” Aronson, 1988

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6
Q

deception BPS guidelines

A

deception should be avoided if at all possible

it should only be used if there is no alternative and if the benefits outweigh the costs

should not be used if participants are likely to feel unhappy about it once they are made aware

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7
Q

deception

A

participants have the right not to experience deception in research

avoiding deception is not always possible, as giving participants the full details of research may cause a change in their natural behaviour (due to demand characteristics)

therefore, although it should be minimised, it’s acceptable when:

  • there is no alternative to deception
  • the level of dececption or its consequences are minor
  • the scientific benefit of the research outweighs the costs of deception
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8
Q

deception dealing

A

participants should receive a full debriefing in which they are informed of the full details of the research, inclduing the deception they experienced

a debriefing should ensure that participants are comfortable with their deception, leaving in a “frame of mind that is at least as sound as when they entered” Aronson, 1988

if not, they have the right to withdraw their data from the investigation

before the study, psychologists may also gain prior general consent by informing participants about the general aims, explaining that deception will be used (without explaining how this will occur).

Participants can then give their consent knowing they will experience deception.

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9
Q

Informed consent BPS

A

where possible, participants should be informed of the full details of the research before agreeing to take part

participants should never feel coerced or pressurised into taking part in research (eg bribes or rewards)

for children, who cannot give their own informed consent, consent should be given by a parent or a guardian

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10
Q

informed consent

A

participants have the right to give their informed consent before taking part in research, by being made aware of an experimenter’s aims, procedures and anticipated findings, and signing their agreement to take part

full informed consent is only given if a participant signs their agreement to take part in the investigation having been told:

  • aim of the experiment
  • the full procedure
  • the anticipated findings
  • their rights (eg right to withdraw)
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11
Q

informed consent dealing

A

before the study, psychologists gain presumtive consent from other members of the target population (who will not be taking part in the actual research)

people similar to the participants are told the full details of the study and are asked if they would give their consent to take part (based on the info provided)

if this group agrees, researches can presume that the actual participants will feel the same, gaining their presumtive consent

before the study, psychologists also gain prior general consent by informing participants about the general aims, without giving too much detail about the research. Participants can then give their consent knowing roughly what they will experience.

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12
Q

right to withdraw BPS

A

participants should be told they have the right to withdraw at the start of the experiment and at key points throughout

without question, participants can withdraw themselves and their data provided during the study

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13
Q

right to withdraw

A

participants have the right to withdraw themselves from the experiment, including any data they have provided

as they have the right to withdraw at any time during the experiment (and without question), this right should be made clear from the start of the research and at key point throughout the experiment

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14
Q

right to withdraw dealing

A

at the end of the study, participants should receive a debriefing in which they are informed of the full details of the research

if participants were not informed of their right to withdraw at the start of the research (eg due to deception), they at least have the right to withdraw their data from the investigation at this point

although the right to withdraw should be made clear from the start of the research, participants should also be reminded of this right at key points throughout the experiment

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15
Q

privacy and confidentiality BPS

A

where possible, participants should remain anonymous: they should be referred to by participant numbers rather than names

participant names should only be taken if there is a need to contact participants at a later date (eg to effectively debrief them)

participants data must not be shared with anyone unless agreed in advance

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16
Q

privacy and confidentiality

A

participants have the right to experience privacy and confidentiality

this means that their personal details (name age etc) and any information obtained during the research (eg their research data) must not be shared with others (unless they give their informed consent for this to occur)

any information that is recorded about a participant must be made anonymous, so that it is not possible to identify them in a published report

17
Q

privacy and confidentiality dealing

A

before the study, participants privacy can be respected by gaining their full informed consent, in which they are made aware of their right to privacy and confidentiality

if participants details need to be shared with other professionals, this should be made clear so participants can sign their agreeement (or not) to provide certain information