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Flashcards

Ethical research & the replication crisis

Sian Allen Psychology English 26 cards

Cards in this deck (26)

  1. 1BPS Code of Human Research Ethics (2nd edition, 2014)General principles that are applicable to all research contexts with human participants
  2. 2BPS Code of Ethics & Conduct (2018)To guide all BPS members in their day-to-day professional conduct
  3. 3BPS Guidelines for Psychologists Working with AnimalsGuidelines for all members whose work involves animals
  4. 4Which key issues do the BPS guidelines cover?- Coercion
    - Consent
    - Deception
    - Debriefing
    - Withdrawal
    - Anonymity & confidentiality
    - Protection of participants
    - Giving advice
  5. 5CoercionParticipation in research is voluntary & they can leave anytime they want > they should not incur any penalties for not participating
    Equally rewards should not be so great that they are coerced into taking part
  6. 6ConsentWhenever possible, participants should have to give informed consent before taking part in the study
  7. 7Deception- Sometimes necessary as some things cannot be studied without it
    - Also avoids demand characteristics
    - Should be used sparingly & justified
  8. 8DebriefingAllows participants to fully understand the research
    - Deception MUST be disclosed in the debrief (what it was & why it was necessary)
    - Mood repair tasks can be included if things like negative mood have been induced
    - Additional sources of information/help can also be added if sensitive topics have been covered
  9. 9Withdrawal- Participants can choose to revoke their consent at any point of the study
    - They can also request for their data to be destroyed & excluded from the analysis
  10. 10Anonymity- Wherever possible data should be collected anonymously
    - Sometimes this isn't possible (interviews) > data should be anonymised in these cases & original data should be destroyed
  11. 11Confidentiality- To do with who has access to your data
    - This need is stronger for non-anonymised data
    - Informed consent needs to include = whom you share your data with, how long you'll keep it, how you'll store it, GDPR requirements
  12. 12Protection of participants- Participants shouldn't be subject to more harm than they would encounter in their daily life
    - Contact details must be provided in order to deal with any complaints/unforeseen consequences
  13. 13Giving advice- If a participant shows signs of mental or physical illness & does not appear aware, the researcher has a duty to inform them
    - The researcher should however not give advice on serious issues unless they are specifically qualified
  14. 14Limits to anonymity & confidentialityResearchers have a duty of care towards their participants = anonymity/confidentiality can be broken when the participant is:
    - In danger (e.g., abuse)
    - Indicates to be committing a crime > in some instances, admits to past crimes
  15. 15Do you need informed consent for observational research?- In public spaces: No (people can expect to be observed anyway)
    - In privately owned spaces (e.g., shopping malls or clubs): yes, consent would be needed from the owner
  16. 16Research with vulnerable people * Which populations are considered vulnerable? *- Children younger than 16
    - Prisoners
    - People with diagnosed MHC
  17. 17Research with vulnerable people- If someone cannot give informed consent, you need additional consent from a caregiver (e.g., a parent)
    - Materials should be adjusted to fit your participants > a lack of understanding means NO informed consent
  18. 18What ethical issues are there after data collection?- Plagiarism
    - Duplication
    - Data falsification
    - Authorship violations
  19. 19PlagiarismPassing off others' work as your own
  20. 20DuplicationTrying to disguise old work as new
  21. 21Data falsificationEditing data to give it a more favourable result or making it up entirely
  22. 22Authorship violationsDenying contributors credit or inventing fake co-authors
  23. 23Examples of Questionable Research Practices (QPRs)- Dropping participants from the dataset
    - Dropping conditions from an experiment
    - HARKing
    - Running multiple studies but only reporting fewer/those you feel are favourable
  24. 24What can QPRs result in?A replication crisis
  25. 25What is a replication crisis?People can publish effects that do not exist therefore subsequent studies looking for the same effect fail to replicate the results
  26. 26Reproducibility project- Replication attempts for over 100 studies were conducted
    - 97% of original studies showed significant effects > 36% of replications did so
    - Strength of effects were about 1/2 in the replications > 47% were comparable to the originals

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Psychology (PS1813 - Research methods) Flashcards on Ethical research & the replication crisis , created by Sian Allen on 27/05/2022.
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Sian Allen
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