Chapter 4_ Ethical Guidelines for Psychology Research
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Chapter 4: Ethical Guidelines for
Psychology Research
What is Ethics?
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Derived from the Greek word “ethos” meaning “ways of living”
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Concerns moral principles of human conduct
The Milgram Obedience Studies
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Told that participants were being split between “teachers” and “learners” (learners being confederates)
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Teachers were instructed to punish learners for mistakes; through shocks which would increase in voltage
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Voltage would eventually be as high as 450-volt shocks (which after 300-volts you wouldn’t hear screams anymore ●
The simple requirement of “continue”, “the experiment requires you to continue” ●
65% of the participants obeyed - delivering 450-volt shocks to the learner
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Only 2-3 participants (out of hundreds) would refuse to administer the first 15-volt shock
Illustrate a Difficult Ethical Balance
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Ethical questions
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Was it ethical to put teacher participants through such a stressful experience?
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Were there lasting effects of study after participants had been debriefed
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Balancing risk to participants with the benefit of society
Core Ethical Principles
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Nuremberg Code (not a formal law)
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Declaration of helsinki
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The Belmont Report (USA)
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APA Code of Ethics
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Tri-Council Policy Statement: Ethical Conduct for Research Involving Humans (Canada)
Nuremberg Code
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Following WWII, the Nuremberg trials revealed the horrors of medical experiments conducted on concentration camp victims in Nazi-occupied Europe and this results in the Nuremberg Code
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It is a point statement delimiting the permissible medical experimentation on human subjects
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It is not a formal law in any nation; but it influences the ethical research laws of many countries
Declaration of Helsinki
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A set of ethical principles in regards to human experimentation
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Developed originally in 1964 for the medical community by the World Medical Association
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It is widely regarded as the cornerstone of human research ethics
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Many national leaders have signed the declaration
The Belmont Report
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US based guidelines for researchers to follow
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In 1976, a commission of physicians, ethicists, philosophers, scientists and other citizens gathered in Maryland and intensively discussed basic ethical principles researchers should follow
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Principle of respect for persons
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Principle of beneficence
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Principle of justice Guidelines for Psychologists: APA Ethical Principles ●
Governs psychologists in their role as a scientist, educator and practitioner
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Covers a wide range of issues:
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Clinical/counseling issues
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E.g., fees, competence, relations with clients
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Organizational issues ■
E.g., advertising, org conflicts, consulting
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Academic issues
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E.g., teaching, supervision, relationships
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Research issues
APA Code of Ethics - Research
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E.g., publication credit, honesty in reporting, REB/IRB approval, sharing data, plagiarism, reviewing manuscripts prior to publication
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Doing research
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E.g., informed consent, integrity, respect for person’s rights and dignity, debriefing, deception
Belmont Plus Two: APA Code of Ethics
1.
Beneficence and nonmaleficence ○
Treat people in ways that benefit them
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Don’t cause suffering
2.
Fidelity and responsibility
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Establish trust
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Responsibility professional behaviour (in research, teaching and clinical practice)
3.
Integrity
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Strive to be accurate, truthful and honest in roles as researcher, clinician and teacher
4.
Justice
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Strive to treat all groups of people fairly
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Those who are in the study will benefit from the research
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Recognize that people are autonomous agents
5.
Respect for people’s rights and dignity ○
Rights to privacy, giving consent, and participate confidentially
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Understand that some populations may be less able to give autonomous consent Belmont Report
APA Ethical Principles
Description
Beneficence
a)
Beneficence and nonmaleficence Treat people in ways that benefit them. Do not cause suffering. Conduct research that will benefit society.
b)
Fidelity and responsibility
Establish relationships of trust; accept responsibility for professional behavior (in research, teaching, and clinical practice).
c)
Integrity
Strive to be accurate, truthful, and honest in one’s role as researcher, teacher, or practitioner.
Justice
d)
Justice
Strive to treat all groups of people fairly. Sample research participants from the same populations that will benefit from the research. Be aware of biases.
Respect for persons
e)
Respect for people’s rights and dignity
Recognize that people are autonomous agents. Protect people’s rights, including the right to privacy, the right to give consent for treatment or research, and the right
to have participation treated confidentially. Understand that some populations may be less able to give autonomous consent, and take precautions against coercing such people.
Tri-Council Policy Statement
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It applies to all research involving humans, conducted in Canada or abroad, by researchers working under the auspices of one or more institution(s) eligible for funding by federal agencies:
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CIHR/IRSC: Canadian Institutes of Health Research ○
NSERC/CRSNG: Natural Sciences and Engineering Research Council of Canada
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SSHRC/CRSH: Social Sciences and Humanities Research Council
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Three complementary core principles
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Respect for persons
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Concern for welfare
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Justice 1) Respect for Persons
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Respect for free and informed consent
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Anticipated harms, risks, and benefits
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What is involved in the study?
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Simple, uncomplicated language
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Outlines: procedures, risks, and benefits of the research
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Option to decide whether to participate (right to give consent)
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Deception
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Omission
: Researchers withheld some details of the study from participants ■
E.g., Batman study
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Commission: Researchers actively lied to participants ■
E.g., Milgram study
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Debriefing
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Full disclosure of the research purpose and other important information
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Usually done at the end of the study
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Most important when you have any type of deception
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Given the option to decide not to include their data
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Respect for vulnerable persons
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Children, infirm, those unable to understand, those in distress
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Respect for privacy and confidentiality
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E.g., quoting subjects and data storage
Respect for Privacy and Confidentiality
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Anonymous Study
: Researchers don’t collect any potential identifying information (names,
birthdays, photos, etc.) ●
Confidential Study
: Researchers collect some identifying information, but prevent it from being disclosed
2) Concern for Welfare
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Includes physical, emotional, spiritual, social and economic welfare ○
E.g., not leaving study upset, in pain, embarrassed or humiliated, poorer. Etc.
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Avoiding humiliating, embarrassing or shaming participants
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Respect for autonomy of participants
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E.g., can choose to quit at any time or not include their data
3) Justice
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Treat people fairly and equitably
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Equal distribution of benefits and burdens of research
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No segment of population unfairly burdened by harms of research
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Don’t neglect/discriminate against individuals or groups who may benefit
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Don’t abuse the power imbalance in the relationship between research and participant
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Don’t undermine the respect for the participants with conflict of interest
Ethical Principles in Practice
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Research ethics boards
: committee responsible for interpreting ethical principles and ensuring research using human participants is conducted ethically.
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Not all research goes to the ethics boards; minor issues will go to peer review process; larger issues will go to ethic board
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Universities
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Hospitals
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Governments
Carleton University’s Research Ethics Board (CUREB)
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All research involving humans conducted by faculty, staff or students at carleton must be approved by CUREB
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External researchers conducting studies at carleton or with carleton faculty, staff or students
Submission Process
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Submission form (included info about the study risks, benefits, recruitment process, procedures, data storage, etc.)
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Supervisor approval form (if you’re a student)
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TCPS Core-2022 Training Certificate ●
Copies of all written communications (recruitment materials, screening forms, informed consent forms, debriefing forms, questionnaires)
Ethical Decision Making: A Thoughtful Balance
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Ethical decision making requires a balance of priorities
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We need to weigh the potential harm to human or animal participants against what the knowledge gained from the research will contribute to society
Harms Vs. Benefits
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REB has an ethical obligation to review scientific validity and design of research. If benefits deemed unlikely or exaggerated, REB can require changes to satisfy need that benefits outweigh harms
Tri-Council Policy Statement
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Three complementary core principles
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Respect for persons
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Concern for welfare
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Justice Respect for Persons ●
Are participants giving consent to participate without coercion, undue influence, or too many incentives?
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Is the consent they are providing informed? ●
If deception is being used, is it needed for the research project, and do they provide debriefing with the opportunity for the participants to refuse consent/withdraw their data?
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Do the participants have the decision-making capacity to provide consent? (respecting vulnerable persons) ○
Can also be done by parents or primary caregivers for informed consent ●
How is the data provided by participants stored and protected? (privacy and confidentiality of data)
Concern for Welfare
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Does the study protect the welfare of their participants (physically, emotionally, spirituality,
socially, economically)?
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If there are risks to welfare, how are the researchers minimizing this risk?
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Is consent to participate an ongoing process?
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E.g., giving the option to skip questions, or withdrawal from the study
Justice
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Why choose this group of prospective participants, and not a broader or a narrower one?
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Is there a sound rationale for who is included in and excluded from participation in the research?
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Who will be exposed to the risks, and who will experience the possible benefits?
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Is there a power imbalance that could cause problems for consent and the study procedures?
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Is there a population of people who are inappropriately excluded (sexism, racism, ageism, ableism, etc.)?
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Is there a conflict of interest?
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Is there a power imbalance?
Minimization of Harm
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Avoid, prevent or minimize harm to others
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Sample’s participation in research must be essential to achieving scientific and societally important aims that can’t be achieved without participation of human sample’s
Other Ethical Standards for Research
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Research misconduct
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○
Fabrication
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Inventing
data to fit their hypotheses instead of reporting what actually happened
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Falsification ○
Influencing
the study’s results towards the hypothesis
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Selectively deleting cases, influencing participants to respond in a certain way
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Plagiarism, including self-plagiarism
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Representing the ideas or words of others as one’s own
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APA citations
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Direct quotes: “Don’t plagiarize” (Derochers, 2024 p.1)
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Paraphrasing: It is highly recommended not to plagiarize (Derochers, 2024)
Other Ethical Standards for Research
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Animal Research
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“Carleton University is committed to ensuring that the use of animals in research and in teaching conforms to the most rigorous ethical standards while actively supporting cutting edge science.” (CUREB, no date)
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Carleton University Animal Care Committee (ACC)
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Animal care guidelines and the three R’s
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Replacement
: Alternatives to using animals when possible ■
Refinement
: How can research procedures and aspects of animal care be altered to reduce animal distress? ■
Reduction
: Adopting a research design that requires the fewest number of animals possible
Terms
Debrief
To inform participants afterward about a study’s true nature, details, and hypotheses.
Principle of Respect for Persons
An ethical principle from the Belmont report stating that research participants should be treated as autonomous agents and that certain groups deserve special protection.
Informed
Consent
The right of research participants to learn about a research project, know its risks and benefits, and decide whether to participate.
Principle of Beneficence
An ethical principle from the Belmont report stating that researchers must take precautions to protect participants from harm and to promote their well-being.
Anonymous Study
A research study in which identifying information is not collected, thereby completely protecting the identity of participants.
Principle of Justice
An ethical principle from the Belmont report calling for a fair balance between the kinds of people who participate in research and the kinds of people who benefit from it.
Confidential Study
A research study in which identifying information is collected, but protected from disclosure to people other than the researchers.
Institutional Review Board (IRB)
A committee responsible for ensuring that research using human participants is conducted ethically.
Deception
The withholding of some details of a study from participants (deception through omission) or the act of actively lying to them (deception through commission).
Data Fabrication
A form of research misconduct in which a researcher invents data that fit the hypothesis.
Data Falsification
A form of research misconduct in which a researcher influences a study’s results, perhaps by deleting observations from a data set or by influencing participants to act in the hypothesized way.
Plagiarism
Representing the ideas or words of others as one’s own; a form of research misconduct.
Self-Plagiarism
A potentially unethical practice in which researchers recycle their own previously published text, verbatim and without attribution, in a subsequent article.