week 4 - Ethics in social research Flashcards
Why be ethical
- The best preparation for ethical behavior is to eternalize a sensitivity to ethical concerns, to adopt a serious professional role, and to interact regularly with other researchers.
- The scientific community also demands ethical behavior for all researchers without exception.
Scientific misconduct
-The research community and agencies that fund research are opposed to unethical behaviour called scientific misconduct. Research fraud and plagiarism are part of scientific misconduct.
Actually, Scientific misconduct occurs whenever a researcher falsifies or distorts the data or the methods of data collection, or plagiarizes the work of others.
Research fraud
-occurs when a researcher fakes or invents data that he or she did not really collect or fails to honestly and fully report how a study has been conducted
Plagiarism
-occurs when a researcher “steals” the ideas or writings of another or uses them without citing the source. This includes stealing the work of another researcher, an assistant, or a student and misrepresenting it as one’s own work.
Power relations
- The researcher’s credentials, training, and professional role and the place of science in modern society legitimate the power and make it into a form of expert authority. Some ethical issues involve an abuse of power and trust.
- A researcher’s authority to conduct social research and to earn the trust of peers is always accompanied by an immutable ethical responsibility to guide, protect, and oversee the interests of the people being studied.
- When looking for ethical guidance, researchers can turn to a number of resources to include: professional colleagues, ethical advisory committees, institutional review boards or human subjects committees at academic institutions, codes of ethics by professional associations and writings on ethics in research.
The law and codes of ethics recognize some clear prohibitions:
-Never cause unnecessary or irreversible harm to subjects;
secure prior voluntary consent, when possible;
-Never unnecessarily humiliate and degrade subjects or release harmful information about specific individuals that was collected for research purposes.
Today, researchers widely recognize these to be violations of two fundamental ethical principles
- Avoid physical harm;
- Obtain informed consent
Physical harm
- An ethical researcher anticipates risks before beginning a study. This includes basic safety concerns such as safe buildings, furniture, and equipment;
- The researcher accepts moral and legal responsibility for injury from participation in research and terminates a project immediately if he or she can no longer guarantee the physical safety of research participants.
informed consent
- is an agreement by participants stating that they are willing to be in a study after they learn something about what the research procedure will involve.
- People need to know what they are being asked to participate in so that they can make an informed decision.
- Governments vary in the requirement for informed consent. The Canadian federal government does not require informed consent in all research involving human subjects, although there is a strong recommendation that informed consent be received
- Researchers should get written informed consent unless there are good reasons for not obtaining it (e.g., covert field research, use of secondary data) as judged by a research ethics board (REB).
- Research ethics board (REB): is an institutional body responsible for assessing whether a proposed research project involving human subjects is ethical or not.
- Informed consent statements provide specific information such as a general statement about the kinds of procedures involved and the uses of the data.
informed consent statements contain the following:
- A brief description of the purpose and procedure of the research, including the expected duration of the study
- A statement of any risks or discomfort associated with participation
- A guarantee of anonymity and the confidentiality of records
- The identification of the researcher and of where to receive information about subjects’ rights or questions about the study
- A statement that participation is completely voluntary and can be terminated at any time without penalty
- A statement of alternative procedures that may be used
- A statement of any benefits or compensation provided to subjects and the number of subjects involved 8. An offer to provide a summary of findings
Special populations
-people who lack the necessary cognitive competency to give real informed consent, people in a weak position who might compromise their freedom to refuse to participate in a study, or groups who have been historically exploited and oppressed.
The Tri-Council policy statement
-specifies that researchers must have respect for vulnerable persons. Some populations or groups of research participants are not capable of giving true voluntary informed consent
Privacy
-researchers invade a research participant’s privacy when they probe into beliefs, back-grounds, and behaviours in a way that reveals intimate private details.
Anonymity
-people remain anonymous or nameless. The subject’s identity is protected, and the individual remains unknown or anonymous.
Confidentiality
-can include information with participant names attached, but the researcher holds it in confidence or keeps it secret from public disclosure. The researcher releases data in a way that does not permit linking specific individuals to responses and presents it publicly only in an aggregate