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Improving Patient Consent Processes: A Case Study in Clinical Trials
[Amélioration des processus de consentement patient : une étude de cas dans le domaine des essais cliniques]

Author

Listed:
  • Negar Armaghan

    (MRM - Montpellier Research in Management - UPVD - Université de Perpignan Via Domitia - UM - Université de Montpellier)

  • Isabelle Bourdon

    (MRM - Montpellier Research in Management - UPVD - Université de Perpignan Via Domitia - UM - Université de Montpellier)

Abstract

The management of the patient consent process is a particularly important issue in clinical research. In France, the general principle is the obligation to provide clear and precise information to all patients and to obtain their informed consent. The aim of this paper is to model the impact of a blockchain solution on the patient consent process in clinical trials. Indeed, blockchain is a technology that enables the provision of new healthcare services, such as the traceability of patient consent. We conducted a case study of patient consent processes in clinical research, applying business process management (BPM) modelling principles. The results highlight the ability of blockchain to manage consent processes, ensuring fast and reliable access to relevant consent information for stakeholders

Suggested Citation

  • Negar Armaghan & Isabelle Bourdon, 2025. "Improving Patient Consent Processes: A Case Study in Clinical Trials [Amélioration des processus de consentement patient : une étude de cas dans le domaine des essais cliniques]," Post-Print hal-05084868, HAL.
    • Handle: RePEc:hal:journl:hal-05084868
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