How has learning about the history of research ethics impacted your view of biomedical research?
In looking at the studies you reviewed for your PICOT question, do you feel that today’s researchers adequately protect the rights of human subjects? If not, what additional measures do you recommend?
Must accurately and fully discuss the topic for the week and provide professional examples. Also, must completely answer the entire initial question. Provide must two references.
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Introduction:
The study of research ethics is an essential component of biomedical research, as it provides the framework for ethical conduct of research studies. It is important for medical college students to understand the history of research ethics and the current regulations in place, as they will be responsible for conducting research studies in the future. In this response, I will discuss how learning about the history of research ethics has impacted my view of biomedical research and provide recommendations for additional measures to protect the rights of human subjects in research studies.
Answer 1:
Learning about the history of research ethics has impacted my view of biomedical research by providing me with a better understanding of the ethical issues that can arise in research studies. I have learned about the unethical experiments that were conducted in the past, such as the Tuskegee syphilis study, which highlighted the importance of informed consent and the protection of participants’ rights in research studies. Additionally, learning about the current regulations in place, such as the Belmont Report and the Common Rule, has emphasized the importance of ethical conduct in research studies. Overall, learning about the history of research ethics has reinforced the importance of conducting ethical research studies to protect the rights of human subjects.
Answer 2:
In looking at the studies reviewed for my PICOT question, I do not feel that today’s researchers adequately protect the rights of human subjects. While researchers are required to obtain informed consent from participants, some studies have demonstrated that participants may not fully understand the details of the study or the potential risks involved. Additionally, some studies have been criticized for the lack of diversity in participant populations, which can result in biased findings. To address these issues, I recommend that researchers provide clear and concise explanations of the study to participants, including any potential risks. Researchers should also strive to recruit a diverse population of participants to ensure that their findings are applicable to a broad range of individuals. Additionally, ethical oversight boards should thoroughly review research studies to ensure that they comply with ethical regulations and protect the rights of human subjects.
References:
1. National Institutes of Health. (n.d.). Belmont Report. Retrieved from https://www.hhs.gov/ohrp/regulations-and-policy/belmont-report/index.html
2. U.S. Department of Health and Human Services. (2017). 45 CFR 46: Protection of human subjects. Retrieved from https://www.hhs.gov/ohrp/regulations-and-policy/regulations/45-cfr-46/index.html
