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Hi, need to submit a 1250 words essay on the topic Ethics in Research Case Study.Download file to see previous pages... 8). On the other hand, informed consent informs the performance of ethical resea
Hi, need to submit a 1250 words essay on the topic Ethics in Research Case Study.
Download file to see previous pages...8). On the other hand, informed consent informs the performance of ethical research by ensuring that all research subjects are well conscious of what they are getting drawn into. It is crucial for all researchers to remain committed to superior levels of professional conduct, which encompass ethically acceptable research behaviours. The purpose of this paper is to examine Scenario A, identifying and discussing the ethical dilemmas presented in a comprehensive manner. All health-related research projects, involving human subjects call for the assessment of potential risks to the subjects. Researchers have an explicit responsibility to guarantee the integrity of their studies, especially when human subjects are involved. As a consequence, institutions require researchers to uphold the organizations’ good name, as well as the vocation to which they belong. Institutions typically require researchers to observe legal, professional and ethical duties in all aspects of research (List 2008, p. 672). The purpose of ethics approval is, therefore, to guarantee that all research endeavours comply with the established guidelines, including the proper conduct of human and animal research. This means that researchers should only engage in research that adhere to accepted ethical standards, which the researchers are able to perform. It is the obligation of the researcher to accomplish and sustain superior levels of intellectual integrity in the conduct of research. Ethics approval ensures the protection of the researchers, institutions and research participants, both animal and human. Additionally, ethics approval protects the entire community from harm caused by unethically performed research (Tauber 2005, p. 18). In scenario A, the researchers failed to seek ethics approval, hence undermining the overall ethicalness of the research. Typically, ethics approval is acquired before embarking on participant recruitment or prior to commencing data collection. Ethically sound institutions do not grant ethics approval in retrospect. Formal approval notification is typically required to ascertain that ethics approval has occurred. Whenever researchers fail to seek the approval of an institution before embarking on the research, they compromise the ethicality and acceptability of all ensuing findings (Babbie 2010, .p. 51). Before guaranteeing ethics approval, institutional ethics committees identify potential ethical issues and guarantee that the researchers satisfactorily address these issues. Ethics committees typically utilize accepted guidelines to assess research studies thus ensuring the protection of the rights and welfare of human subjects. Essentially, ethics approval is essential to deter the incident of risk or potential harm to research participants. Another ethical dilemma inherent in the scenario concerns the issue of seeking informed consent from all study participants. This involves the process of informing participants regarding the study in order to allow them make informed decisions with regard to engaging in the research. Educating subjects regarding the research starts after the initial contact and persists for the entire duration of their engagement in the study (List 2008, p. 514). This means that all information provided to participants through recruitment letters, study description sheets and advertisements should be understandable.
