ethical issues

Cards (24)

  • ways of dealing with ethical issues
    risk assessment and management
    consent and debriefing
    research ethics committee
  • can a high risk low benefit study go ahead?
    no
  • can a low risk low benefit study go ahead?
    no
  • can a high risk high benefit study go ahead?
    maybe
  • can a low risk high benefit study go ahead?
    yes
  • how to prevent possible risks
    identifying possible risks
    considering vulnerable groups
    balancing risk and benefit
    ethical descion making
  • reducing risks
    informed consent procedures
    monitoring and support
    debriefing
    pilot studies (test run)
    ethical reviews
    allowing withdrawal
    confidentiality measures
  • what are the 3 types of consent?
    presumptive
    prior general
    retrospective
  • presumptive consent
    a similar group of people are asked if the study is acceptable
    if the group agrees the original participant’s consent is ‘presumed’
  • prior consent
    participants give their permission to take part in several studies - including one that will involve deception
    by consenting the participants are effectively consenting to being deceived
  • retrospective consent
    participants are asked for their consent having already taken part in the study
    they may not have been aware of participation and may have been subject to deception
  • research ethics committee (REC)
    ensures research is conducted responsibly
    essential for upholding ethical standards in psychology
  • participants POV on anonymity/ confidentiality
    the general data protection regulation (GDPR) makes confidentiality a legal right
  • participants POV on deception
    this prevents being able to give truly informed consent
    however there is a difference between withholding info and falsely informing participants about the aims of the study
    both are deception but the 1st is more acceptable
  • participants POV on informed consent
    this is necessary so that participants can make a decision on whether to participate, without full info they cannot do this
    certain participants are unable to give informed consent (e.g. children)
  • participants POV on privacy
    people expect to be observed by others in a public place, so this is acceptable
    however there isn’t universal agreement on what constitutes a public place (e.g. listening to some convo on a bus - public or private?)
  • participants POV on right to withdraw
    participants often do not fully understand what is involved and / or may simply not imagine how they would feel in certain situations
    thus it is important for them to leave a study if it was not what they expected
  • participants POV on protection from harm
    people are robust and can tolerate some anxiety
    however, it is reasonable for a participant to expect at the end of the study to be in the same ‘state’ they were in the beginning (e.g. not less happy/ confident)
  • researcher POV on anonymity and confidentiality
    it may nit be possible to keep info anonymous / confidential because some details of a study may lead to an individual’s identification
  • researcher POV on deception
    if participants know the research aims this would spoil the study
    it might be argued that some deception is relatively harmless and/ or can be compensated for by adequate debriefing
  • researcher POV on informed consent
    asking for informed consent may reduce the meaningfulness of the research because the researcher has to provide info that could reveal the study’s aims
    this may affect the participants behaviour as they know the aim of the study
  • researcher POV on privacy
    researches do not wish to alert participants to the fact that they are being observed because that is likely to affect the participants behaviour
  • researcher POV on right to withdraw
    the loss of participants may bias the study’s findings because the ones that remain may be more highly motivated or less emotionally sensitive
  • researcher POV on protection from harm
    it may not be possible to estimate harm before conducting a study - however, any study should be stopped as soon as any harm is apparent