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Group Research Proposals. Change in submission and presentation dateProposals now due FRIDAY 27th APRIL at 9.30 amPresentations will now occur in Week 7i.e. AFTER THE EASTER BREAK. What are research ethics?.
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1. Research Ethics JN602
Week 05
Chapter 3, pp. 65-71
3. What are research ethics? Ethics and ethical principles extend to all spheres of human activity. They apply to our dealings with each other, with animals and the environment. They should govern our interactions not only in conducting research but also in commerce, employment and politics. Ethics serve to identify good, desirable or acceptable conduct and provide reasons for those conclusions. (NHMRC, 1999, p.13)
4. Principles of research ethics National Health and Medical Research Council (1999)
Integrity
Respect for persons: individuals should be treated as autonomous agents and that persons with diminished autonomy are entitled to protection (p.16)
Beneficience: maximise possible benefits, minimise possible harm
Justice: who ought to receive the benefits of research and bear its burdens (p.16)
5. Ethical principles (Veal, 2005) No harm should befall research subjects
Subjects should take part freely
Participation should be based on informed consent
6. Expression of ethical principles (NHMRC, 1999, p.23) Integrity: commitment to the search for knowledge, to recognised principles of research conduct and in the honest and ethical conduct of research and dissemination and communication of results
Respect for persons: regard for the welfare, rights, beliefs, perceptions, customs and cultural heritage, both individual and collective, of persons involved in research
7. Expression of ethical principles (cont.) Beneficence: researchers responsibility to minimise risks of harm or discomfort to participants in research projects. Each research protocol must be designed to ensure that respect for the dignity and well being of the participants takes precedence over the expected benefits to knowledge.
Justice: within a population, there is a fair distribution of the benefits and burdens of participation in research and, for any research participant, a balance of burdens and benefits.
8. The Research Process and Ethics
9. Enforcement of research ethics Universities, hospitals, professional bodies and government departments have codes of ethics
Ethics Committees (also known as Institutional Review Boards in the U.S.A.) must approve all research with humans and with animals
E.g. UB Human Research Ethics Committee
http://www.ballarat.edu.au/ard/ubresearch/hdrs/ethics/humanethics/hrec.shtml
Potential loss of professional indemnity if code not followed
10. Minimising Harm Ensure privacy/confidentiality/anonymity/ security of information received.
Use fictitious names when reporting results.
Seek permission to quote when identification unavoidable (eg, Mayor, Managing Director).
11. Free choice (Veal, 2005) Also known as voluntary consent
Subjects must not be coerced into participating
even in captive group situations
Free choice not possible in:
Some observational research
Some type of participant observation
12. Informed consent Participants should be fully informed about the nature and purpose of the research
Some grey areas when full information might bias results
13. The importance of informed consent The Milgram Obedience experiments
Re-creation: http://www.wernersplace.com/obedience2.htm
Original videotape: http://video.google.com.au/videoplay?docid=-1606897927982220440
The Tea Room Trade
http://www.research.uwaterloo.ca/ethics/human/resources/index.htm
14. Obtaining consent(NHMRC, 1999) (a) provision to participants, at their level of comprehension, of information about the purpose, methods, demands, risks, inconveniences, discomforts, and possible outcomes of the research (including the likelihood and form of publication of research results); and
(b) the exercise of a voluntary choice to participate.
15. Unequal or dependent relationships(NHMRC, 1999, p.42) Situations where unequal power relationships exist between participants and researchers or where participants occupy junior or subordinate positions in hierarchically structured groups.
Examples include:
persons with chronic conditions or disabilities and their carers;
patients and health care professionals;
students and teachers;
prisoners and prison authorities; and
employees and their employers or supervisors.
16. General research ethics(Veal, 2005) Researchers should be competent
Research should be informed by a literature review
Plagiarism is unethical
All contributors should be acknowledged
Falsification of results is unethical
17. Example: Ethics in survey research Interviewee issues
Interviewer issues
Sampling
Politics
18. Interviewee issues Privacy
Anonymity
Time
Comprehension
Knowledge of subject matter
19. Interviewer Issues Interviewers background
Interviewer integrity: ethics
Interviewer knowledge and preparation
Bias occurs when the interviewers opinion influences the answer
20. Sampling Who should you ask in order to get useful information?
Depends on the research question
You want your sample to be representative of the group you are interested in
Probability sampling
Non-probability sampling
21. Politics(SLT, 2003) Researcher: What if the test results are favourable?
Product Manager: Why, well launch the product nationally, of course
R: And if the results are unfavourable?
PM: They wont be. Im sure of that.
R: But just suppose they are.
PM: I dont think we should throw out a good product just because of one little market test.
R: Then why test?
PM: Listen, this is a major product introduction. Its got to have some research behind it.
22. Differences between interviewer-assisted and self-completion surveys Interview
Open
Confronting
Clarification
Assistance
Slower
Accuracy affected by:
Interviewer bias
Social acceptability Self-completion
Private
Confidential
Needs accurate qus
No assistance
Faster for respondent
Accuracy affected by:
Misunderstanding
Length of questionnaire
23. Ethics - summary The rights of respondents are always the most important.
Respondents cooperation in research is entirely voluntary at all stages.
Respondents should not be subject to negative effects from taking part in a survey.
The respondents anonymity must be strictly protected.