CDIS 455 Ethics in Research
Chapter 2: Ethics
WHAT ARE ETHICS?
Research ethics are defined as rules of conduct that have developed over time based on sound and logical research practices.
Key Aspects of Ethics:
Beliefs: Personal convictions that guide individuals in their moral decisions.
Conduct: The behavior exhibited by individuals or groups in their actions.
Conscience: The inner sense of what is right or wrong in one's conduct or motives.
Conventions: Established norms or practices within societies or groups.
Decency: The quality of being polite and respectful.
Values: Core principles or standards that guide behavior and decision-making.
Principles of Integrity: Adhering to moral and ethical standards in all actions.
Protection of Human Rights:
Ethics are fundamentally designed to protect human rights, ensuring that all individuals are treated fairly and justly in any research or experimental context.
Moral Conduct
Ethics can be viewed through two main lenses:
Relativism:
Holds that rules of conduct vary according to individual needs, customs, and historical evolution.
Absolutism:
Maintains that rules of conduct are consistent and should always be the same, regardless of context or individual circumstances.
What is the IRB?
IRB: Institutional Review Boards are essential groups in the research process.
Composed of no less than 5 experts as well as laypeople with diverse backgrounds to ensure thorough and adequate reviews of research proposals.
IRB Duties:
Evaluate potential risks involved in the research.
Assess safeguards to protect participants.
Recommend modifications to the study design as needed.
Code of Ethics
Code of Ethics: A formalized and written set of principles that guide the conduct of experimentation.
ASHA Code of Ethics: A specific ethical framework within the field of audiology and speech-language pathology.
Belmont Report Ethical Principles:
Identified three basic ethical principles relevant to research involving human subjects:
Respect for Persons: Acknowledging autonomy, informed consent, and the obligation to protect individuals with diminished autonomy.
Beneficence: Obligation to minimize harm and maximize benefits to participants.
Justice: Fair distribution of the benefits and burdens of research.
Participants in Research
Research plans typically involve human subjects referred to as “participants.”
Researchers select participants based on the study's purpose and methodology.
Informed Consent Forms:
Critical documents used in research to obtain consent from participants and inform them about participating in the study.
Basic Elements of Consent Forms:
Explanation of Procedures: Detailed description of what participation involves.
Risks or Discomforts: Potential risks or discomforts associated with participation.
Benefits: Expected benefits of participating in the study.
Alternative Procedures: Options available to participants outside of the proposed study.
Confidentiality: Assurance of how participants' data will be kept private.
Legal Rights: Participants' rights in relation to the research.
Signatures: Confirmation and acknowledgment of the participant’s consent.
Etc.: Additional information as necessary.
Research Issues
Common ethical issues faced in research include:
Privacy: Safeguarding participant information and data.
Withholding Treatment: Ethical considerations about whether to provide or withhold treatment in research settings.
Collecting Data: The methods used to gather data must adhere to ethical standards.
Attrition: The dropout rates of participants and its implications on the research outcomes.
Dishonesty: Issues related to misconduct or unethical behavior in reporting results.
Conflicts of Interest: Situations where personal interests may compromise the integrity of the research.
What is Evidence-Based Practice?
Evidence for best practice in fields such as:
Audiology: Study and treatment of hearing and balance disorders.
Speech-language pathology: Assessment and treatment of speech, language, and communication disorders.
Autonomy: Acknowledging and respecting individuals' rights to make informed choices regarding their own healthcare.
References
Meline, T. (2010). A research primer for communication sciences and disorders. Pearson.