Cited by 26Telemedicine and Telehealth ImplementationEthics in Clinical ResearchStatistical Methods in Clinical Trials

Decentralisation in Clinical Trials and Patient Centricity: Benefits and Challenges

Sinha, Shubhadeep D., Chary Sriramadasu, Sreenivasa, Raphael, Ruby, Roy, Sudeshna·2024·Pharmaceutical Medicine

Abstract

Decentralised clinical trials (DCTs) encompass various terms such as virtual, home-based, remote and siteless trials. The objectives of DCTs are to enhance the ease of participation for patients in clinical trials by minimising or removing the necessity for trial subjects to travel to the trial sites. This approach has been shown to reduce drop-out rates, increase study effectiveness and ultimately get life-altering drugs to market faster-saving sponsors billions. At the outset, DCTs deploy a wide range of digital technologies to collect safety and efficacy data from study participants, providing study treatments and performing investigations from the comfort of the patient's own home. The aim of decentralised trials includes patient centricity, enhanced efficacy in clinical trial conduct and generating real-world data. This is done by not only making it convenient for the patient to participate in the trial execution, but also involving them from the planning stage and taking their inputs during designing of trials and consenting documentation, understanding their treatment requirements and designing the studies accordingly. Various regulatory authorities have published guidelines governing DCT principles, especially after the coronavirus disease 2019 (COVID-19) experience of undertaking multicentric clinical trials. Both United States Food and Drug Administration (USFDA) and European Medicines Agency (EMA) have newer, recently updated guidelines to capture this growing reality to undertake clinical trials using patient technology or patient-centric technologies. Other regulatory agencies are accepting data generated using decentralised and patient-centric technologies and making an effort to include elements of decentralised trials in their regulatory guidelines. Decentralised trials follow a hybrid approach to have a balanced mix of remote and in-person data collection and trial procedures. Decentralised and patient-centric approaches are the future of any organisation for the conduct of clinical trials. Globally, all sponsor pharmaceutical companies must start undertaking drug development and clinical trials using a decentralised approach while keeping patient centricity in mind.

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Crossref · 10.1007/s40290-024-00518-x

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Authors
Sinha, S. D., Chary Sriramadasu, S., Raphael, R., & Roy, S.
Affiliations
Hetero Drugs (India) (IN)
Corresponding author
Sinha, Shubhadeep D.
Venue
Pharmaceutical Medicine
Published
2024-03
Volume
38
Issue
2
Pages
109-120
ISSN
  • 0265-0673 (ISSN-L)
  • 1178-2595
  • 1179-1993
OpenAlex
W4392564369
Cited by
26
References
1
Citations by year
2026: 7 · 2025: 18 · 2024: 1
FWCI
2.30
Type
journal article
Language
en
Open access
closed
Locations
  • Pharmaceutical Medicine (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Telemedicine and Telehealth Implementation
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Ethics in Clinical Research
  • Physical Sciences › Mathematics › Statistics and Probability › Statistical Methods in Clinical Trials
Keywords
decentralized clinical trials, patient-centricity, remote data acquisition, digital health technologies, real-world data, clinical trial regulation, FDA guidance, EMA guidelines, trial participant retention
MeSH terms
COVID-19, Clinical Trials as Topic, Humans, Patients, Politics, United States

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