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Ethics in Research
Source:
https://www.slideshare.net/PennVilla
nueva/chapter-2-ethical-principles-of-
research
Ethics
Politics of Research
Ethics
 What are ethics?
 What are common
ethical issues that
seem to surface in
research?
 When should ethical
issues be considered?
Ethics
 Ethics: principles for guiding decision
making and reconciling conflicting values
 People may disagree on ‘ethics’ because it is
based on people's personal value systems
 What one person considers to be good or
right may be considered bad or wrong by
another person
Major approaches to ethics
 Deontological Approach
 This approach states that we should
identify and use a Universal code when
making ethical decisions. An action is
either ethical or not ethical, without
exception.
 Ethical skepticism
 This is the relativist viewpoint, stating
that ethical standards are not universal
but are relative to one's particular
culture and time.
 Utilitarianism
 This is a very practical viewpoint, stating
that decisions about the ethics of a
study should depend on the balance of
the consequences and benefits for the
research participants and the larger
society.
 The utilitarian approach is used by most
people in academia (such as Institutional
Review Boards).
 "Do the potential benefits outweigh the
risks associated with this research?"
Ethical Concerns to the Research Community
1. The relationship between society
and science.
 Many research ideas come from areas
considered important in society.
 The federal government and other
funding agencies use grants to affect
the areas researchers choose to
examine.
2. Professional issues.
 The primary ethical concern here is fraudulent activity by scientists.
Cheating or lying are never defensible.
 Two related issues are partial publication(publishing several articles
from the data collected in one large study) and duplicate publication
(publishing the same results in more than one publication).
 Partial publication is usually not unethical for large research studies
where partial reports of data are likely.
 Duplicate publication is sometimes acceptable when the results are
being reported to different audiences in publications tailored to
those particular audiences.
3. Treatment of research participants.
 This is probably the most fundamental
ethical issue.
 It involves insuring that research
participants are not harmed physically
or psychologically.
Ethical Guidelines for Research with Humans
 One set of guidelines specifically developed
to guide research conducted by educational
researchers is the AERA Guidelines.
 The AERA is the largest professional
association in the field of education, and is
also known as the American Educational
Research Association.
Informed Consent
 This is the process of providing the research
participants with information enables them to make
an informed decision as to whether they want to
participate in the research study.
 State the purpose of the research and describe the procedures to be followed.
 Describe any potential risks or discomforts the participant may encounter.
 Describe any potential benefits from participation.
 Describe extant to which results will be kept confidential.
 Give a list of names the participants may contact with any questions they have.
 State that participant is voluntary and that they are free to withdraw from the
study at any time.
Informed Consent with Minors as
Research Participants
 Consent must be obtained from parents
or guardians.
 Assent must also be obtained from
minors who are old enough or have
enough intellectual capacity to say they
are willing to participate.
Deception
 Providing false information to the participant about the nature
and/or purpose of the study
 It is discouraged by the AERA, but not disallowed in all cases.
 Sometimes deception is required in order to conduct a valid research study. The
researcher must justify the use of deception.
 If deception is used the following are very important:
 Debriefing is an interview with the research participant providing an opportunity
for the experimenter to reveal deceptive aspects of the study and for the
participant to have any questions about the study answered.
 Dehoaxing: informing the participant about deceptive aspects of the
research study
 Desensitizing: eliminating any stress or other undesirable feelings the
study may have created
Freedom to Withdraw
 Participants must be informed that they are
free to withdraw from the study at any time
without penalty.
 If you have a power relationship with the
participants you must be extra careful to make
sure that they really do feel free to withdraw.
Protection from Mental and Physical Harm
 This is the most fundamental ethical issue
confronting the researcher.
 Educational research generally poses
minimal risk to participants.
Economic Regulation of Research
 Economic regulation is the issue of who
sponsors your research as well as how much
money you get.
 It's the ethical duty of a researcher to get their
results published somewhere. This is called
dissemination of your research, and it requires
that you find the most appropriate and scholarly
outlet that you can.
Political Regulation of Research
 Historically, governments have had to put serious
restrictions on researchers. In fact, the origin of codes of
research ethics can be traced to the NUREMBERG CODE,
a list of rules established by a military tribunal on Nazi
war crimes during World War II. The principles outlined
in the Nuremberg Code include:
 Voluntary consent
 Avoidance of unnecessary suffering
 Avoidance of accidental death or disability
 Termination of research if harm is likely
 Experiments should be conducted by highly qualified people
 Results should be for the good of society and unattainable by
any other means
 The Nuremberg Code was followed by the 1948 U.N. Declaration of
Human Rights and the 1964 Helsinki accord.
 In 1971 (and revised in 1981), the U.S. government initiated guidelines
for all federally funded research. Most federal agencies followed the lead
of HEW (now HHS) because this list of rules could be applied generically
to both medical and nonmedical research. The HEW GUIDELINES were:
 Subjects should be given a fair explanation of the purpose and procedures of the research
 Subjects should be given a description of any reasonable risks or discomforts expected
 Subjects should be told of any possible benefits to be obtained by participating
 Researchers should disclose any alternative procedures that might be advantageous to the
subject
 Researchers should offer to answer any questions subjects may have during the research
 Subjects should be told they are free to withdraw and discontinue participation at any time
 One of the outcomes of the HEW guidelines was the
establishment of INSTITUTIONAL REVIEW BOARDS
(IRBs) at colleges and universities across America. At
first, IRBs were seen as a hindrance on academic
freedom by faculty researchers, but they came to be
accepted, especially after 1981 when the revised HHS
guidelines exempted most social science and criminal
justice research from full review by creating a category
of "expedited" review.
Institutional Review Board
 This is a board consisting of professionals and lay people who review
research proposals to insure that the researcher will adhere to ethical
standards in the conduct of the research.
 Researchers must submit a Research Protocol to the IRB for review
 Three of the most important categories of review are exempt studies,
expedited review, and full board review
 Much educational research falls in the exempt category: being exempt
from certain requirements and full committee review because the study
involves no or minimal risk
 Studies with children, prisoners, and fetal participants are never exempt
 Even if your study ultimately falls in the exempt category, it is still
essential that you follow the ethical guidelines
There are three ways, and three ways only, to
encourage participation ethically (Senese 1997):
 Anonymity: Promise and keep your promises of anonymity. After
identifying your sampling frame, try to forget about taking names or
any other unique identifiers. Reassure people that you won't go to the
media. Fill them in on what journal outlet you have planned.
 Confidentiality: This is what you should promise if you can't keep
anonymity. In other words, use confidentiality if you can't guarantee
anonymity. It requires that you guarantee that no one will be
individually identifiable in any way by you, that all your tables,
reports, and publications will only discuss findings in the aggregate.
 Informed Consent: Be honest and fair with your subjects. Tell them
everything they want to know about your research. Be aware of any
hidden power differentials that might be pressuring them to
participate.
CASE: TEAROOM TRADE
 was the name of a book published by a sociologist
named Laud Humphreys in 1970 who posed as a
"watchqueen" in public restrooms to observe
homosexual behavior
 After every liaison where an old man would seduce
some "chicken hawk" with money for an oral sex
experience, Humphreys would jot down the license
plate number of each old man's vehicle. Then, he
had a friend in the police department trace the
addresses. He would then visit the old men at
home and pressure them into giving him an
interview.
 The case stands as a classic example of invasion of
privacy.
CASE: TUSKEGEE SYPHILIS STUDY
 was conducted from 1932 to 1974 and
involved the withholding of penicillin from
black male sharecroppers so the
government could find out the long term
effects of syphilis
 Similar experiments went on with the U.S.
military involving nerve gas and nuclear
radiation. The CIA also performed bizarre
mind control experiments involving LSD,
ESP, hypnosis, and surgery.
 The moral of all this is not to conduct secret
testing on unsuspecting subjects.
CASE: ZIMBARDO'S PRISON SIMULATION
 was a study by psychologist Philip Zimbardo in
1972 that took Stanford University undergrads and
made some of them guards and some of them
prisoners in a mock underground dungeon for a
planned two week stay.
 The experiment had to be cancelled after six days
because by then, the student-guards became quite
sadistic, really getting into their roles. The prisoners
were also becoming quite mental.
 The experiment tells a story about psychological
harm and informed consent, since the subjects did
not know what they were getting into.
Discussion Scenario (s)
 After a field study of deviant behavior during
a riot, law enforcement officials demand that
the researcher identify those people who were
observed looting. Rather than risk arrest as
an accomplice after the fact, the researcher
complies.
 Ethical issues?
 A research questionnaire is circulated among
students as part of their university registration
packet. Although students are not told they
must complete the questionnaire, the hope is
that they will believe they must – thus
ensuring a higher completion rate.
 Ethical Issues?

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ethic in research.pptx

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  • 24. Ethics  What are ethics?  What are common ethical issues that seem to surface in research?  When should ethical issues be considered?
  • 25. Ethics  Ethics: principles for guiding decision making and reconciling conflicting values  People may disagree on ‘ethics’ because it is based on people's personal value systems  What one person considers to be good or right may be considered bad or wrong by another person
  • 26. Major approaches to ethics  Deontological Approach  This approach states that we should identify and use a Universal code when making ethical decisions. An action is either ethical or not ethical, without exception.
  • 27.  Ethical skepticism  This is the relativist viewpoint, stating that ethical standards are not universal but are relative to one's particular culture and time.
  • 28.  Utilitarianism  This is a very practical viewpoint, stating that decisions about the ethics of a study should depend on the balance of the consequences and benefits for the research participants and the larger society.
  • 29.  The utilitarian approach is used by most people in academia (such as Institutional Review Boards).  "Do the potential benefits outweigh the risks associated with this research?"
  • 30. Ethical Concerns to the Research Community 1. The relationship between society and science.  Many research ideas come from areas considered important in society.  The federal government and other funding agencies use grants to affect the areas researchers choose to examine.
  • 31. 2. Professional issues.  The primary ethical concern here is fraudulent activity by scientists. Cheating or lying are never defensible.  Two related issues are partial publication(publishing several articles from the data collected in one large study) and duplicate publication (publishing the same results in more than one publication).  Partial publication is usually not unethical for large research studies where partial reports of data are likely.  Duplicate publication is sometimes acceptable when the results are being reported to different audiences in publications tailored to those particular audiences.
  • 32. 3. Treatment of research participants.  This is probably the most fundamental ethical issue.  It involves insuring that research participants are not harmed physically or psychologically.
  • 33. Ethical Guidelines for Research with Humans  One set of guidelines specifically developed to guide research conducted by educational researchers is the AERA Guidelines.  The AERA is the largest professional association in the field of education, and is also known as the American Educational Research Association.
  • 34. Informed Consent  This is the process of providing the research participants with information enables them to make an informed decision as to whether they want to participate in the research study.  State the purpose of the research and describe the procedures to be followed.  Describe any potential risks or discomforts the participant may encounter.  Describe any potential benefits from participation.  Describe extant to which results will be kept confidential.  Give a list of names the participants may contact with any questions they have.  State that participant is voluntary and that they are free to withdraw from the study at any time.
  • 35. Informed Consent with Minors as Research Participants  Consent must be obtained from parents or guardians.  Assent must also be obtained from minors who are old enough or have enough intellectual capacity to say they are willing to participate.
  • 36. Deception  Providing false information to the participant about the nature and/or purpose of the study  It is discouraged by the AERA, but not disallowed in all cases.  Sometimes deception is required in order to conduct a valid research study. The researcher must justify the use of deception.  If deception is used the following are very important:  Debriefing is an interview with the research participant providing an opportunity for the experimenter to reveal deceptive aspects of the study and for the participant to have any questions about the study answered.  Dehoaxing: informing the participant about deceptive aspects of the research study  Desensitizing: eliminating any stress or other undesirable feelings the study may have created
  • 37. Freedom to Withdraw  Participants must be informed that they are free to withdraw from the study at any time without penalty.  If you have a power relationship with the participants you must be extra careful to make sure that they really do feel free to withdraw.
  • 38. Protection from Mental and Physical Harm  This is the most fundamental ethical issue confronting the researcher.  Educational research generally poses minimal risk to participants.
  • 39. Economic Regulation of Research  Economic regulation is the issue of who sponsors your research as well as how much money you get.  It's the ethical duty of a researcher to get their results published somewhere. This is called dissemination of your research, and it requires that you find the most appropriate and scholarly outlet that you can.
  • 40. Political Regulation of Research  Historically, governments have had to put serious restrictions on researchers. In fact, the origin of codes of research ethics can be traced to the NUREMBERG CODE, a list of rules established by a military tribunal on Nazi war crimes during World War II. The principles outlined in the Nuremberg Code include:  Voluntary consent  Avoidance of unnecessary suffering  Avoidance of accidental death or disability  Termination of research if harm is likely  Experiments should be conducted by highly qualified people  Results should be for the good of society and unattainable by any other means
  • 41.  The Nuremberg Code was followed by the 1948 U.N. Declaration of Human Rights and the 1964 Helsinki accord.  In 1971 (and revised in 1981), the U.S. government initiated guidelines for all federally funded research. Most federal agencies followed the lead of HEW (now HHS) because this list of rules could be applied generically to both medical and nonmedical research. The HEW GUIDELINES were:  Subjects should be given a fair explanation of the purpose and procedures of the research  Subjects should be given a description of any reasonable risks or discomforts expected  Subjects should be told of any possible benefits to be obtained by participating  Researchers should disclose any alternative procedures that might be advantageous to the subject  Researchers should offer to answer any questions subjects may have during the research  Subjects should be told they are free to withdraw and discontinue participation at any time
  • 42.  One of the outcomes of the HEW guidelines was the establishment of INSTITUTIONAL REVIEW BOARDS (IRBs) at colleges and universities across America. At first, IRBs were seen as a hindrance on academic freedom by faculty researchers, but they came to be accepted, especially after 1981 when the revised HHS guidelines exempted most social science and criminal justice research from full review by creating a category of "expedited" review.
  • 43. Institutional Review Board  This is a board consisting of professionals and lay people who review research proposals to insure that the researcher will adhere to ethical standards in the conduct of the research.  Researchers must submit a Research Protocol to the IRB for review  Three of the most important categories of review are exempt studies, expedited review, and full board review  Much educational research falls in the exempt category: being exempt from certain requirements and full committee review because the study involves no or minimal risk  Studies with children, prisoners, and fetal participants are never exempt  Even if your study ultimately falls in the exempt category, it is still essential that you follow the ethical guidelines
  • 44. There are three ways, and three ways only, to encourage participation ethically (Senese 1997):  Anonymity: Promise and keep your promises of anonymity. After identifying your sampling frame, try to forget about taking names or any other unique identifiers. Reassure people that you won't go to the media. Fill them in on what journal outlet you have planned.  Confidentiality: This is what you should promise if you can't keep anonymity. In other words, use confidentiality if you can't guarantee anonymity. It requires that you guarantee that no one will be individually identifiable in any way by you, that all your tables, reports, and publications will only discuss findings in the aggregate.  Informed Consent: Be honest and fair with your subjects. Tell them everything they want to know about your research. Be aware of any hidden power differentials that might be pressuring them to participate.
  • 45. CASE: TEAROOM TRADE  was the name of a book published by a sociologist named Laud Humphreys in 1970 who posed as a "watchqueen" in public restrooms to observe homosexual behavior  After every liaison where an old man would seduce some "chicken hawk" with money for an oral sex experience, Humphreys would jot down the license plate number of each old man's vehicle. Then, he had a friend in the police department trace the addresses. He would then visit the old men at home and pressure them into giving him an interview.  The case stands as a classic example of invasion of privacy.
  • 46. CASE: TUSKEGEE SYPHILIS STUDY  was conducted from 1932 to 1974 and involved the withholding of penicillin from black male sharecroppers so the government could find out the long term effects of syphilis  Similar experiments went on with the U.S. military involving nerve gas and nuclear radiation. The CIA also performed bizarre mind control experiments involving LSD, ESP, hypnosis, and surgery.  The moral of all this is not to conduct secret testing on unsuspecting subjects.
  • 47. CASE: ZIMBARDO'S PRISON SIMULATION  was a study by psychologist Philip Zimbardo in 1972 that took Stanford University undergrads and made some of them guards and some of them prisoners in a mock underground dungeon for a planned two week stay.  The experiment had to be cancelled after six days because by then, the student-guards became quite sadistic, really getting into their roles. The prisoners were also becoming quite mental.  The experiment tells a story about psychological harm and informed consent, since the subjects did not know what they were getting into.
  • 48. Discussion Scenario (s)  After a field study of deviant behavior during a riot, law enforcement officials demand that the researcher identify those people who were observed looting. Rather than risk arrest as an accomplice after the fact, the researcher complies.  Ethical issues?
  • 49.  A research questionnaire is circulated among students as part of their university registration packet. Although students are not told they must complete the questionnaire, the hope is that they will believe they must – thus ensuring a higher completion rate.  Ethical Issues?