Research ethics form the cornerstone of scientific inquiry, ensuring that research is conducted responsibly, transparently, and with respect for human and animal subjects

AiresChavezPerea 21 views 13 slides Aug 09, 2024
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About This Presentation

Research ethics form the cornerstone of scientific inquiry, ensuring that research is conducted responsibly, transparently, and with respect for human and animal subjects. As the foundation of trust between researchers, participants, and the public, ethical principles guide the conduct of research t...


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ETHICS IN CONDUCTING RESEARCH

Ethics in Research

Research Ethics Involves the application of fundamental ethical principles to planning, conducting & publishing of research. Ethical considerations in research are set of principles that guide your research designs and practices. Scientist and researchers must always adhere to a certain code of conduct when collecting data from people. These ethical considerations are protect the right of research participants, enhance research validity and maintain scientific or academic integrity.

Why do research ethics matters? Research ethics matter for scientific integrity, human rights and dignity, and collaboration between science and society. These principles make sure that the participant in studies is voluntarily, informed and safe for research subjects. Avoiding research ethics will also lower the credibility of your research because it’s hard for others to trust your data if your method is morally questionable. Even if the idea is valuable to society, it’s doesn’t justify violating human rights or dignity of your study participants.

Types of Ethical Issues There are several ethical issues you should always pay attention to in your design and these issues can overlap with each other. Voluntary Participation – means that all research subject are free to choose to participate without any pressure or coercion. All participants are able to withdraw from, or leave, the study in any point without feeling an obligation to continue and don’t need to provide a reason for leaving the study.

Informed Consent – refers to a situation in which all potential participants receive and understand all the information ( information about the study’s benefits, risk, funding, how long the study will take and institutional approval ) they need to decide whether they want to participate. If your collecting data from people with low literacy, make sure to verbally explain the consent form to them before they agree to participate. For participants with very limited English, you should always translate the study materials or work in Filipino or on their own dialect with an

interpreter so they have all the information in their first language. In research with children, you will often need informed permission for their participation from their parents or guardian. Anonymity – means that you don’t know who the participants are and you can’t link any individual participant to their data. It can only guarantee by not collecting any personally identifying information – for example, names, phones numbers, email addresses, IP addresses, physical characteristics, phots or videos. data pseudonymization- alternative method where you

replace identifying information about participants. When conducting a research to college students, ask them to enter demographic information including their age, gender identity, nationality and ethnicity so it may not be possible to other people to identify individual participants. Confidentiality – means that you know who the participants are but you remove all identifying information from your research. All participants have the right to privacy, so you should protect their personal data for as long as you store or use it by taking steps to safeguard it and prevent any threats to data privacy.

Potential for Harm As a researcher, you must consider all possible sources of harm to participants. Psychological harm : sensitive questions or tasks may trigger negative emotions such as shame or anxiety. Social harm : participation can involve social risk, public embarrassment, or stigma.

Potential for Harm Physical harm : pain or injury can result from study procedures. Legal harm : reporting sensitive data could lead to legal risks or breach of privacy. Note: Make sure to disclose all possible risks of harm to participants before the study to get informed consent. If there is a risk of harm, prepare to provide participants with resources or counselling or medical services if needed.

Communicating results can sometimes involve ethical issues. Good science communication is honest, reliable, and credible. It’s best to make your result as transparent as possible. Take steps to actively avoid plagiarism and research misconduct wherever possible. Plagiarism- means submitting other works as your own. Although it can be unintentional copying someone else’s work without proper credit amounts to stealing. Self-plagiarism- is when you re-publish or re-submit parts of your own paper or reports without proper citing your original work.

You may benefit from presenting your ideas as new and original even though they’ve already been published elsewhere in the past. You may also infringe on your own previous publisher’s copyright, violating an ethical code. Research Misconduct – means falsifying data, manipulating data analysis, or misinterpreting results in research report. It’s a form of academic fraud. It is a serious ethical issue because it can undermine academic integrity and institutional credibility.