Protection of Human Subject Participants in Nursing Research

Peer Responses:

Number: A Minimum of 2 to Peer Posts, at least one on a different day than the main post
Length: A minimum of 150 words per post, not including references
Citations: At least one high-level scholarly reference in APA per post from within the last 5 years
Peer Post:
For this discussion, I have chosen to discuss the human rights and bioethics issue of consent. Informed consent is more than just a form that is signed. It is comprised of a process in which the research subject has a total comprehension of the research and its associated risks. It is clearly defined in ethical codes and regulations for human subject research. When clinical research is conducted, it is essential that informed consent is obtained. Informed consent is a process through which a competent subject, “after having received and understood all the research-related information, can voluntarily provide his or her willingness to participate in a clinical trial” (Manti & Licari, 2018).
The principle of consent is “one of the bedrocks of clinical ethics and research ethics” (Melnyk & Fineout-Overholt, 2019, p. 694). As far as research and research studies go, participation should be voluntary. It is the duty of the researchers to present enough information to the potential subjects that they can make an informed choice whether or not to participate in the research study. We all have autonomy over our bodies, and obtaining informed consent is based on this fact. It is incumbent upon the researchers to provide enough information that the subjects understand the risks of the research as well as the benefits.
The first principle of the Nuremberg Code states that, “the voluntary consent of the human subject is absolutely essential.” Similarly, the United Nations International Covenant on Civil and Political Rights states that “no one shall be subjected without his free consent to medical or scientific experimentation.” (Gelinas et al., 2016).
Gelinas, L., Wertheimer, A., & Miller, F. G. (2016). When and Why Is Research without Consent Permissible? Hastings Center Report, 46(2), 35–43.
Manti, S., & Licari, A. (2018). How to obtain informed consent for research. Breathe, 14(2), 145–152.
Melnyk, B. M., & Fineout-Overholt, E. (2019). Evidence-based practice in nursing & healthcare: a guide to best practice. Wolters Kluwer.

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