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Signing Research Consent Forms 1
Signing Research Consent Forms 1
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Institution
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SIGNING RESEARCH CONSENT FORMS 2
investigating certain aspects of care. When human participants are involved in such research
processes, it is paramount that healthcare providers and researchers ensure that participants
have a clear understanding of the research process, the associated risks and benefits of
participations, and their role in the research (Burke, 2021). Healthcare providers must ensure
that patients participating in this research understand the research trials and consent form.
full understanding of the procedure or treatment, the risks, alternatives, and benefits involved
(Burke, 2021).
Nurses must advocate for their patients by ensuring that the patients have full
therefore important. While the informed consent forms entail all information related to the
research, it is important for the nurse to explain the risks and benefits of the study to the
participants (Sil & Das, 2017). Doing this ensures that what was missed by the participants
while reading the forms is verbally addresses and contentious issues are addressed. After
doing so, the nurse should further ask the participants questions related to the content of the
forms, possible risks and benefits that the participants may experience in their participation,
and what is expected of them in the research. Doing this will help identify gaps in
information presented in the consent forms and initiating strategies to address these gaps.
SIGNING RESEARCH CONSENT FORMS 3
References
https://www.registerednursing.org/nclex/informed-consent/
Sil, A., & Das, N. K. (2017). Informed Consent Process: Foundation of the Researcher-
https://doi.org/10.4103/ijd.IJD_272_17