The intersection of clinical trial management and patient advocacy: How research professionals can promote patient rights while upholding clinical excellence
Independent Researcher, Texas, USA.
Review
World Journal of Biology Pharmacy and Health Sciences, 2024, 20(01), 296–308.
Article DOI: 10.30574/wjbphs.2024.20.1.0787
Publication history:
Received on 01 September 2024; revised on 13 October 2024; accepted on 15 October 2024
Abstract:
The purpose of this study was to investigate the intersection of clinical trial management and patient advocacy, focusing on how research professionals can promote patient rights while upholding clinical excellence. As clinical trials evolve to become more patient-centered, balancing ethical obligations with scientific rigor remains a significant challenge. This paper explores key concepts such as informed consent, patient engagement, data privacy, and the ethical responsibilities of research professionals. Additionally, it examines the role of emerging technologies, including mobile health applications, wearable devices, telemedicine, and blockchain, in enhancing patient advocacy and improving trial outcomes.
A thorough literature review and analysis were conducted to identify the challenges faced in integrating patient advocacy into clinical trial management. The study also highlights the critical role of research professionals in ensuring that patient rights are respected while addressing the complexities of global clinical trials, where varying ethical standards pose additional challenges.
The findings suggest that patient-centric approaches, supported by digital tools, can significantly improve the ethical integrity of clinical trials, ensuring greater inclusivity, accessibility, and retention of participants. However, these innovations also raise concerns regarding data security, necessitating the implementation of robust cybersecurity measures to protect patient confidentiality.
In conclusion, the study recommends the adoption of decentralized clinical trials and the harmonization of global regulatory frameworks to ensure consistent ethical standards. Research professionals must prioritize patient welfare while embracing technological advancements that offer opportunities for more efficient and inclusive clinical research. By striking this balance, clinical trials can better serve both scientific progress and the ethical imperatives of patient advocacy.
Keywords:
Clinical trial management; Patient advocacy; Decentralized trials; Digital health tools; Informed consent; Data privacy.
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Copyright information:
Copyright © 2024 Author(s) retain the copyright of this article. This article is published under the terms of the Creative Commons Attribution Liscense 4.0