ethical issues

    Cards (28)

    • Informed Consent
      At a basic level, prospective participants in studies
      should know what they are getting into before they
      get into it. Informed consent involves making
      participants aware of the aims of the research, the
      procedures, their rights (including the right to
      withdraw partway through the investigation should
      they so wish), and also what their data will be used
      for. Participants should then make an informed
      judgement whether or not to take part without
      being coerced (pressured) or feeling obliged.
    • Informed Consent
      From the researcher's point
      of view, asking for informed
      consent may make the
      study meaningless because
      participants' behaviour will
      not be 'natural' as they
      know the aims of the study.
    • Informed consent;
      Participants must be given
      comprehensive information
      concerning the nature and purpose of
      the research and their role in it, in
      order that they can make an informed
      decision about whether to participate.
    • Presumptive consent;
      rather than getting consent
      from the participants
      themselves, a similar group
      of people are asked if the
      study is acceptable. If this
      group agree, then consent
      of the original participants
      is 'presumed’.
    • Prior general consent;
      participants give their
      permission to take part in
      a number of different
      studies including one that
      will involve deception. By
      consenting, participants
      are effectively consenting
      to be deceived.
    • Retrospective consent;
      participants are asked for
      their consent (during
      debriefing) having already
      taken part in the study. They
      may not have been aware of
      their participation or they
      may have been subject to
      deception.
    • Presumptive consent – although the people asked may be similar, they are not the same
      as the participants and so may have views about what is acceptable in psychological
      research that do not reflect those of the participants.
    • Prior general consent – although participants may consent to a notional study, they may
      feel very differently when the actual investigation takes place.
    • Retrospective consent – participants may feel deceived by the fact that they were not
      asked for their permission at the beginning of the study. This was a feature of Milgram's
      obedience study; people felt that 'the damage was already done' by the time Milgram
      asked for consent.
    • Deception means deliberately
      misleading or withholding information
      from participants at any stage of the
      investigation. This is linked to the
      informed consent. Participants who have
      not received adequate information
      when they agreed to take part (or
      worse, have been deliberately lied to)
      cannot be said to have given informed
      consent.
    • Despite that, there are occasions
      when deception can be justified if it
      does not cause the participant undue
      distress.
    • Deception;
      A participant is not told the true
      aims of a study (e.g. what
      participation will involve) and
      thus cannot give truly informed
      consent.
    • As a result of their involvement,
      participants should not be placed at any
      more risk than they would be in their
      daily lives, and should be protected
      from physical and psychological harm.
      Psychological harm includes being made
      to feel embarrassed, inadequate or being
      placed under undue stress or pressure.
    • Protection from Harm
      An important feature of
      protection from harm, as
      mentioned before, is
      participants being reminded
      of the fact that they have
      the right to withdraw from
      the investigation at any
      point.
    • Protection from harm;
      During a research study,
      participants should not experience
      negative physical or psychological
      effects, such as physical injury,
      lowered
      self-esteem or embarrassment.
    • Privacy and Confidentiality
      Participants have the right to control information about
      themselves. This is the right of privacy. If this is invaded, then
      confidentiality should be protected.
      Confidentiality refers to
      our right, enshrined in law
      under the Data Protection
      Act, to have any personal
      data protected.
    • Privacy and Confidentiality
      The right to privacy
      extends to the area
      where the study took
      place such that
      institutions or
      geographical locations
      are not named.
    • Confidentiality;
      Concerns the communication of personal
      information from one person to another, and
      the trust that the information will be
      protected.
      Privacy;
      A person's right to control the flow of
      information about themselves.
    • BPS Code of Conduct
      The British Psychological Society (BPS), like many other professional
      bodies, has its own BPS code of ethics and this includes a set of
      ethical guidelines.
      Researchers have a professional
      duty to observe these guidelines
      when conducting research – they
      won't be sent to prison if they don't
      follow them but they may well lose
      their job.
    • BPS Code of Conduct
      The guidelines are closely matched to the ethical issues we discussed
      last lesson and attempt to ensure that all participants are treated
      with respect and consideration during each phase of research.
      Guidelines are implemented by
      ethics committees in research
      institutions who often use a
      cost-benefit approach to determine
      whether particular research
      proposals are ethically acceptable.
    • It is the responsibility of ethics committees to
      weigh up the costs and benefits of research
      proposals to decide whether the research
      study should go ahead. Benefits might
      include the value or ground-breaking nature
      of the research. Possible costs may be the
      damaging effect on individual participants or
      to the reputation of psychology as a whole.
    • Dealing with Informed Consent
      Participants should be issued with a
      consent letter or form detailing all
      relevant information that might affect
      their decision to participate. Assuming
      the participant agrees, this is then signed.
      For investigations involving children
      under 16, a signature of parental consent
      is required. There are other ways to
      obtain consent, as discussed last lesson.
    • Dealing with Deception and Protection from Harm:
      Debriefing
      At the end of a study, participants
      should be given a full debrief. Within
      this, participants should be made
      aware of the true aims of the
      investigation and any details they
      were not supplied with during the
      study, such as the existence of other
      groups or experimental conditions.
    • Dealing with Deception and Protection from Harm:
      Debriefing
      Participants should also be told
      what their data will be used for
      and must be given the right to
      withhold data if they wish. This
      is particularly important if
      retrospective consent is a
      feature of the study.
    • Dealing with Deception and Protection from Harm:
      Debriefing
      Participants may have natural
      concerns related to their performance
      within the investigation, and so should
      be reassured that their behaviour was
      typical or normal. In extreme cases, if
      participants have been subject to
      stress or embarrassment, they may
      require counselling, which the
      researcher should provide.
    • When participants arrive to take part in
      a study they are given a briefing so they
      can provide informed consent (told
      what they will be asked to do, told some
      or all of the aims of the research, etc.).
      After the research participants will be
      debriefed.
    • Dealing with Confidentiality
      If personal details are held these must be
      protected. However it is more usual to
      simply record no personal details, i.e.
      maintain anonymity. Instead, researchers
      usually refer to participants using numbers
      or initials when writing up the
      investigation. In a case study,
      psychologists often use initials when
      describing the individual or individuals
      involved.
    • Dealing with Confidentiality
      Finally, it is standard
      practice that during briefing
      and debriefing, participants
      are reminded that their
      data will be protected
      throughout the process.