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Ethics and Honesty in Conducting and Reporting Educational Research

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Title: Ethics and Honesty in Conducting and Reporting Educational Research


1
  • Ethics and Honesty in Conducting and Reporting
    Educational Research

2
Two Major Issues
  • Conducting the Research
  • Reporting the Research

3
The Nuremberg Trials
  • The public was outraged to learn of the
    scientific experiments conducted by Nazi
    physicians and scientists during WWII. As a
    result 10 principles to guide research were
    formulated The Nuremberg Code

4
Tuskegee Syphilis Study
  • Poor Black men in the South were not told they
    had syphilis and the available treatment was
    withheld to see what would happen. This went from
    1932-1972. The public was outraged. President
    Clinton issued an apology.

5
The Belmont Report
  • Because of the public outcry, the federal
    government organized the National Commission for
    Protection of Human Subjects of Behavioral and
    Biomedical Research to develop guidelines for
    research with human subjects. This group issued a
    report in 1979 known as The Belmont Report.

6
The Belmont Report
  • Beneficence Do no harm (risks to subjects must
    be balanced against the benefits to them and to
    others)
  • This is not a major problem in agricultural and
    extension education research.

7
The Belmont Report
  • Justice really should be labeled as equality.
    Protects one part of the population from bearing
    the brunt of the research.
  • Are death row inmates involved in potentially
    risky research?
  • Where are garbage dumps located?

8
The Belmont Report
  • Respect for persons allow people to make their
    own decisions about whether or not to participate
    in the research.

9
Federal Regulations
  • In 1991 the Federal Government established Title
    45 Code of Federal Regulations (part 46) to
    govern federally funded research activities.
  • The regulations are administered by the Office
    for Human Research Protections (OHRP)
  • Since NCSU receives federal research money, we
    must abide by these guidelines.

10
Federal Regulations
  • Institutions like NCSU must have an Institutional
    Review Board (IRB) that reviews and approves any
    research involving humans (and animals).
  • This board makes sure our research is in
    accordance with federal guidelines.

11
The IRB
  • The IRB has the authority to
  • approve
  • approve with modifications
  • table, or
  • disapprove any research proposal involving human
    subjects.
  • They also have the authority to suspend or stop
    any research project involving human subjects.

12
The IRB
  • If an investigator conducts human subject
    research without obtaining appropriate IRB review
    and approval, a number of consequences may arise.
    The investigator may be unable to publish his/her
    findings, study data may be confiscated, sources
    of funding may be lost, and ultimately, an
    institution could lose its assurance, thereby
    losing its privilege to conduct research with
    human subjects.

13
IRB Levels of Approval
  • Exempt Determined by the IRB Administrator. At
    NCSU we call this Administrative Review instead
    of exempt.
  • Even if the researcher knows the study is exempt,
    IRB review is required.
  • The IRB must determine it is exempt.

14
So What is Exempt?
  • 1. Research conducted in established or commonly
    accepted educational settings, involving normal
    educational practices, such as (i) research on
    regular and special education instructional
    strategies, or (ii) research on the effectiveness
    of or the comparison among instructional
    techniques, curricula, or classroom management
    methods.

15
So What is Exempt?
  • 2. Research involving the use of educational
    tests (cognitive, diagnostic, aptitude,
    achievement), survey procedures, interview
    procedures or observation of public behavior,
    unless (i) information obtained is recorded in
    such a manner that human subjects can be
    identified, directly or through identifiers
    linked to the subjects and (ii) any disclosure
    of the human subjects' responses outside the
    research could reasonably place the subjects at
    risk of criminal or civil liability, or be
    damaging to the subjects' financial standing,
    employability, or reputation.

16
So What is Exempt?
  • 3. Research involving the use of educational
    tests (cognitive, diagnostic, aptitude,
    achievement), survey procedures, interview
    procedures, or observation of public behavior
    that is not exempt under paragraph (b)(2) of this
    section, if (i) the human subjects are elected
    or appointed public officials or candidates for
    public office or (ii) federal statute(s)
    require(s) without exception that the
    confidentiality of the personally identifiable
    information will be maintained throughout the
    research and thereafter.

17
So What is Exempt?
  • 4. Research, involving the collection or study of
    existing data, documents, records, pathological
    specimens, or diagnostic specimens, if these
    sources are publicly available, or if the
    information is recorded by the investigator in
    such a manner that subjects cannot be identified,
    directly or through identifiers linked to the
    subjects.

18
So What is Exempt?
  • 5. Research and demonstration projects, which are
    conducted by or subject to the approval of
    department or agency heads, and which are
    designed to study, evaluate, or otherwise
    examine (i) public benefit or service programs
    (ii) procedures for obtaining benefits or
    services under those programs (iii) possible
    changes in or alternatives to those programs or
    procedures or (iv) possible changes in methods
    or levels of payment for benefits or services
    under those programs.

19
So What is Exempt?
  • 6. Taste and food quality evaluation and consumer
    acceptance studies, (i) if wholesome foods
    without additives are consumed, or (ii) if a food
    is consumed that contains a food ingredient at or
    below the level and for a use found to be safe,
    or agricultural chemical or environmental
    contaminant at or below the level found to be
    safe.

20
IRB Levels of Approval
  • Expedited If the potential for harm of human
    subjects is neglible, a review from one or more
    committee members is all that is needed.

21
IRB Levels of Approval
  • Full Board Review by the full board with a
    quorum being present.

22
The Review
  • The IRB must see everything the subject will see
    (cover letter, survey instrument, etc.)
  • This must be done before any type of data
    collection.
  • For ongoing projects, you must get IRB approval
    every year.

23
Possible Research Risks
  • Physical Harm
  • Confidentiality (leaking information about a
    participant)
  • Intrusion on Privacy (conducting part of a study
    in a public setting)
  • Emotional/Psychological

24
How to Reduce Risks
  • Have an informed consent form
  • Use code numbers instead of names to identify
    people
  • Destroy raw data when study is over

25
The NCSU IRB
  • http//www.ncsu.edu/sparcs/irb/

26
Two Major Issues
  • Conducting the Research
  • Reporting the Research

27
Scientific Misconduct
  • Basically, there are three major types of
    scientific misconduct
  • fabrication
  • falsification
  • plagiarism or
  • other practices that seriously deviate from those
    that are commonly accepted within the research
    community for proposing, conducting, and
    reporting research.

28
Fabrication
  • Inventing or making up data
  • Did anyone see Krippendorfs Tribe?
  • An anthropologist creates a fictitious lost New
    Guinea tribe using his family members to cover-up
    for his mis-use of grant moneys.
  • This does happen in Academia, but shouldnt

29
Falsification
  • Falsification of data is the selective alteration
    of data collected in the conduct of scientific
    investigation.
  • Falsification also includes the selective
    omission/deletion/suppression of conflicting data
    without scientific or statistical justification.

30
Plagiarism
  • As a general working definition, the Office of
    Research Integrity (a federal agency) considers
    plagiarism to include both the theft or
    misappropriation of intellectual property and the
    substantial unattributed textual copying of
    another's work. It does not include authorship or
    credit disputes.

31
Examples of Plagiarism
  • Use of sources from the internet without
    proper documentation
  • Undocumented use of sources from other written
    materials, i.e. books, magazines, etc.
  • Use of other students work as ones own

32
Citations
  • Quotation marks should be used to indicate the
    exact words of another.
  • Summarizing a passage or rearranging the order of
    a sentence and changing some of the words is
    paraphrasing.
  • Each time a source is paraphrased, a credit for
    the source needs to be included in the text.
  • APA Manual

33
Scientific Misconduct
Source http//www.physicstoday.org/vol-57/iss-11/
p42.htmlcap1
34
Other Examples of Misconduct
  • False citation is the deliberate citing of a
    source for information, when the source does not
    contain that information, with intention to
    mislead.

35
Other
  • Misuses of the refereeing process
  • a) Misappropriation of ideasstealing ideas from
    papers that one referees
  • b) Misappropriation of prioritypublishing an
    idea first by delaying publication of papers that
    one referees

36
One Other Issue - Authorship
  • Conflicts often occur over authorship of research
    papers.
  • For graduate student research, it is common
    protocol to include the major professor and other
    committee members who made substantial
    contributions to the research in the list of
    authors of a paper/manuscript.
  • The graduate student name goes first.

37
What is a substantial contribution?
  • Authorship credit should be based on 1)
    substantial contributions to conception and
    design, or acquisition of data, or analysis and
    interpretation of data 2) drafting the article
    or revising it critically for important
    intellectual content and 3) final approval of
    the version to be published. Authors should meet
    conditions 1, 2, and 3.

From the International Committee of Medical
Journal Editors.
38
Authorship
  • Acquisition of funding, collection of data, or
    general supervision of the research group, alone,
    does not justify authorship.
  • All persons designated as authors should qualify
    for authorship, and all those who qualify should
    be listed.
  • Each author should have participated sufficiently
    in the work to take public responsibility for
    appropriate portions of the content.

39
Fairness
  • Since professors are expected (really required)
    to publish, and typically have a substantial time
    investment in a graduate student research
    project, then students really should make a
    concerted effort to publish their research.
  • If the student doesnt have an inclination to
    publish the research, then the professor should
    have the right to do so of course giving major
    credit to the student.
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