Upon completion of Unit IV, students will be able to: Identify areas of ethical concern in research Know what is ethical and not ethical in research Develop senses of professionalism and moral obligation to observe research ethics
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Research ethics refers to what is possible, and is not possible to do when conducting research Research assumes that researchers have professional and moral obligations to act responsibly in their activities Observing research ethics is a key factor to earn credibility and respect both from research participants and the public at large
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However, ambiguities abound as to what is ethical or not ethical in research Nevertheless, literature highlights a number of key considerations which the researcher should observe in the course of research activities there are a number of expected codes of conduct and general guidelines that should be duly observed by researchers in their activities
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Ethical considerations in research revolve around issues concerning: 1. The responsibility shown towards research participants 2. The consequences and/or usage of the research outcomes, and 3. The accuracy, validity and honesty of research findings
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Often ethical transgressions occur in the course of data collection, interpretation and the way the findings are used Some of the key questions to ask in this regard are: Is data collection based on voluntary participation? Has any harm been done to participants? Is there invasion of privacy? 1 Are participants consented? Are participants forced or duped to provide information? Are confidentiality and anonymity of participant kept? Is some kind of deception involved in data collection? have others’ work been properly acknowledged? 2 Are findings used for beneficial purposes? Is data interpreted for individual or group benefit? 3 Is data genuinely interpreted?
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A. Responsibility towards research participants Refers to respect of the rights of those cooperating with the research This includes: 1. The need to get informed consent of participants This means: - To get consent from the participants on whether or not they are willing to participate or provide information based on their freewill - Respect for voluntary participation i.e. individuals determine for themselves whether or not to be part of a research project
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- Participants are informed about all aspects of a research project which might influence their decision to participate - such as information on the goals of the research, what is expected of them, as well as potential risks and benefits of participation, incl. the right to withdraw - Avoid forcing or duping subjects to provide information
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- Avoiding disguised and covert observation Informed consent assume that participants are able, competent, mature, responsible and willing to provide the required information, and fully comprehend its consequences - However, it is important to note that the right to informed consent is often violated
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2. Respect for privacy of subjects Refers to the right of subjects to provide information under the conditions they want. i.e.. where they want to provide the information when they want to provide it, and under what condition (s) e.g. level of secrecy, they want to provide it The right to privacy is about paying attention to: i. the sensitivity of the information being solicited ii. the location or setting of the research, and iii. disclosure of the study findings
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3. Confidentiality and anonymity Confidentiality refers to: protection of the participants identity i.e. removing all identifying information about individuals from research records and reports. It is an assurance that the information will never be linked to individual participants in public. It means not going public with personal information esp. keeping sensitive information secret Confidentiality encourages honest responses from participants However, there is limit to confidentiality if the legal system becomes involved
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Anonymity ensures that there is no link at all between individual data and the participant The difference between confidentiality and anonymity is that in the first case the researcher actually knows which name is linked to which specific information while in the second s/he does not
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B. Consequences and/or how research outcomes used Relates to damages that could be done to subjects both during the research process and after the results are obtained - i.e. physical, social, psychological, health damages, etc: - Side effects, and short and long term damages such as disability, pain, distress, loss of self-esteem, etc. - Use of results for destructive purposes
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Research should not cause harm to subjects refrain from activities that cause damage to the physical, psychological and emotional well-being of participants Research that harms or poses risks to subjects is incompatible with the fundamental ethical principles
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C. Accuracy, validity, and honesty This refers to: Reporting nothing but the truth: Fair and accurate reporting of findings is the whole mark of good research Avoiding conflict of interest – the researcher should not be influenced by personal gains in interpreting findings Plagiarism and theft – stealing and using others works without properly acknowledging is not allowed Data manipulation (also known as data doctoring), data falsification, and data fabrication are illegal in research
Measures to ensure research ethics 1. The presence of ethical committees – the existence of bodies entrusted with the responsibility to oversee whether ethical rules are observed or not is vital 2. The presence of peer validation- research findings should always be reviewed by peer groups 3. The need to view research findings with care and measured skepticism 4. The presence of the practice of continuous evaluation of results – checking and rechecking of previous findings is essential to correct possible wrong conclusions