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Chapter 3

Chapter 3 discusses ethical issues in psychological research, emphasizing the importance of informed consent, the management of deception, and the necessity of debriefing participants. It highlights the role of Institutional Review Boards (IRBs) in evaluating research proposals to protect participants' rights and welfare, as well as the potential risks and benefits associated with research. The chapter also addresses the ethical responsibilities of researchers and the consequences of failing to adhere to ethical standards.

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0% found this document useful (0 votes)
8 views16 pages

Chapter 3

Chapter 3 discusses ethical issues in psychological research, emphasizing the importance of informed consent, the management of deception, and the necessity of debriefing participants. It highlights the role of Institutional Review Boards (IRBs) in evaluating research proposals to protect participants' rights and welfare, as well as the potential risks and benefits associated with research. The chapter also addresses the ethical responsibilities of researchers and the consequences of failing to adhere to ethical standards.

Uploaded by

kadirefe0910
Copyright
© All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd

08/03/2026

Chapter 3: Ethical Issues


Buse Keskindag, PhD, CPsychol.

keskinda@[Link]

Outline:
ETHICAL ISSUES TO CONSIDER BEFORE BEGINNING RESEARCH

INFORMED CONSENT

DECEPTION IN PSYCHOLOGICAL RESEARCH

DEBRIEFING

REPORTING OF PSYCHOLOGICAL RESEARCH

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Good science:
Each individual scientist has an ethical responsibility to seek knowledge and
to strive to improve the quality of life.

Scientists should
— carry out research in a competent manner;

—report results accurately;

—manage research resources honestly;

— fairly acknowledge, in scientific communications, the individuals who


have contributed their ideas or their time and effort;

—consider the consequences to society of any research


endeavor;

— speak out publicly on societal concerns related to a scientist’s


knowledge and expertise.

To guide ethical decisions, the American Psychological


Association (APA) has formulated an Ethics Code.

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The Internet has changed the way many scientists do research

E.g., collaborations, collecting data ([recording “behaviour” in


chat rooms], surveys [questionnaires,
including personality tests]).

Internet offers many opportunities for the behavioural scientist,


it also raises many ethical concerns

Such as: the difficulty of obtaining adequate informed consent


and providing debriefing, and concerns about protecting
participant confidentiality

ETHICAL ISSUES TO CONSIDER BEFORE BEGINNING


RESEARCH
Prior to conducting any study, the proposed research must be
reviewed to determine if it meets ethical standards.

• Institutional Review Boards (IRBs) review psychological


research to protect the rights and welfare of human
participants.

• Institutional Animal Care and Use Committees (IACUCs)


review research conducted with animals to ensure that animals
are treated humanely.

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The failure to conduct research in an ethical manner can also


lead to significant legal and financial penalties for individuals and
institutions

Following World War II, the Nuremberg War Crimes Court


charged German doctors with crimes against humanity,

Because of performing medical experiments on human beings


without their consent.

the development of the Nuremberg Code => which set rules for
permissible experimentation with human beings.

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THE RISK/BENEFIT RATIO

“Is it worth it?”

members of an IRB rely on a subjective evaluation of the risks and


benefits both to individual participants and to society,

When the risks outweigh the potential benefits, then the IRB does
not approve the research;

When the benefits outweigh the risks, the IRB approves the research.

Quality of research?

“If because of the poor quality of the science no good can


come of a research study, how are we to justify the use of participants’
time,

attention,

and effort

and the money, space, supplies,

and other resources that have been expended on the research


project?”

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Determining Risk
We often think of risk in terms of the possibility of physical injury.

however, participants in social science research risk social or


psychological injury.

E.g. if personal information were revealed to others, a potential for


social risk such as embarrassment

Data related intelligence; personality traits; political, social, or religious


beliefs; and particular behaviours.

A research participant probably does not want this information to


shared with others

Failure to protect the confidentiality of participants’ responses may


increase the possibility of social injury.

E.g. psychological risk => if participants in the study experience


serious mental or emotional stress.

Imagine the stress a participant may experience when smoke


enters the room in which she is waiting.

The smoke may be entering the room so that the researcher can
simulate an emergency (diffusion of responsibility experiment).

Until the true nature of the smoke is revealed, participants may


experience considerable distress.

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when researchers seek to gather information about child abuse


and interpersonal violence

=> asking individuals to describe instances of child abuse or


family violence from their past can be emotionally stressful.

Yet, knowledge of such experiences can help to provide


important insights (e.g., divorce, poor school performance,
criminality).

A researcher is obligated to protect participants from emotional


or mental stress, including, when possible, stress that might arise
due to participants’ misconceptions about the psychological task.

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Minimal Risk
= the harm or discomfort participants may experience in the
research is not greater than what they might experience in their
daily lives or during routine physical or psychological tests

E.g. task: to complete the tests quickly and participant may


receive specific feedback about their performance.

Although there is likely to be stress in this situation, the risk of


psychological injury is likely no greater than that typically
experienced by students

Dealing with Risk


Even if the potential risk is small, researchers should try to
minimize risk and protect participants.

E.g. simply by stating at the beginning of a memory experiment


that the tasks do not measure intelligence or personality
reduces the stress that some participants experience.

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when participants may experience emotional stress in a


psychology experiment, an IRB could require that a independent
psychologist be available to counsel individuals about their
experience

E.g. online research poses difficult ethical dilemmas


in this regard.

However they encourage participants to contact with related


associated or service by providing contact details of it.

data collection should keep participants’ responses anonymous


by asking participants not to use their names or any other
identifying information.

When this is not possible, researchers should keep participants’


responses confidential by removing any identifying information
from their records during the research.

E.g. when testing people on more than one occasion, code


numbers can be randomly assigned to participants at the
beginning of a study.

Only these numbers need appear on participants’ response


sheets.

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Names are linked with the code numbers on a master list, and
access to this list is restricted by keeping it under lock and key.

Making sure participants’ responses are anonymous or


confidential can also benefit the researcher if this leads
participants to be more honest and open when responding

INFORMED CONSENT

informed consent is an essential component of the social


contract between the researcher and the participant.

Informed consent is a person’s explicitly expressed willingness


to participate in a research project based on a clear
understanding of the nature of the research, of the
consequences for not participating, and of all factors that might
be expected to influence that person’s willingness to
participate.

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The U.S. Public Health Service between 1932 and 1972 examined
the course of untreated syphilis in poor African American men
from Macon County, Alabama, who had not given informed
consent.

They were unaware they


Had syphilis and their
disease was left untreated.

Participants’ consent must be given freely, without pressure.

Participants should also know they are free to withdraw their


consent at any time without penalty or prejudice

True informed consent cannot be obtained from certain


individuals, such as the mentally impaired, and young children

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must be obtained from the participants’ parents or legal


guardians

Pressure to participants:

E.g. when university students are asked to fulfill a class


requirement by serving as participants in psychology
experiments, an alternative method of fulfilling the class
requirement must be made available to those who do not wish
to participate in psychological research

In some situations researchers are not required to obtain


informed consent.

E.g. observing individuals’ behaviour in public places without any


intervention.

=> race relations on a college campus by observing the


frequency of mixed-race versus non-mixed-race groups walking
across campus.

The investigator would not need to obtain students’ permission


before making the observations.

Informed consent would be required, if the identity, and


information of specific individuals was going to be recorded.

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DECEPTION IN PSYCHOLOGICAL RESEARCH

In the 1960s, participants in Stanley Milgram’s experiments


were not told that the purpose of the research was to observe
people’s obedience to authority, and many followed the
researcher’s instructions to give severe electric shock to
another human being.

Deception can occur either through neglect, the withholding of


information, or commission, intentionally misinforming
participants about an aspect of the research.

Despite the increased attention given to deception in research


over the last several decades, the use of deception in
psychological research has not declined

One reason: it is impossible to carry out certain kinds of research


without withholding

In other situations, it is necessary to misinform participants in


order to have them adopt certain attitudes or behaviours

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E.g., investigating helping behaviour –

Would participants’ helping behaviour change when they knew


that the study is about helping behaviour?

Although deception is sometimes justified to make it possible to


investigate important research questions, deceiving participants
for the purpose of getting them to participate in research that
involves more than minimal risk is always unethical.

the Ethics Code: “Psychologists do not deceive prospective


participants about research that is reasonably expected to cause
physical pain or severe emotional distress”

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DEBRIEFING

Participants are given this form at the end of the study

When deception has been used in research, debriefing is


necessary to explain to participants the need for deception, to
address any misconceptions participants may have about their
participation.

For all research (with/out deception), as the important goals of


educating participants about the research (rationale, method,
results)

REPORTING OF PSYCHOLOGICAL RESEARCH

Plagiarism

Don’t present substantial portions or elements of another’s


work as your own.

A substantial element can be a single word or short phrase if


that element serves to identify a key idea or concept that is the
result of another’s thinking.

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It is also important to cite the source of material you include in your


paper when you paraphrase

STEPS FOR ETHICAL COMPLIANCE:

-- Review the facts of the proposed research situation (e.g.,


participants, procedure).

—Identify the relevant ethical issues, guidelines, and law.

—Consider multiple viewpoints (e.g., participants, researchers,


institutions, society, moral values).

—Consider alternative methods or procedures and their


consequences, including the consequences of not doing the proposed
research.

To help ensure ethical compliance throughout the research


process, APA has published an Ethical Compliance Checklist

[Link]

formal institutional approval (IRB) must be obtained before


beginning to do research

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