A conceptual model for the development process of confirmatory adaptive clinical trials within an emergency research network

Author:

Mawocha Samkeliso C1,Fetters Michael D2,Legocki Laurie J2,Guetterman Timothy C2,Frederiksen Shirley1,Barsan William G1,Lewis Roger J34,Berry Donald A4,Meurer William J15

Affiliation:

1. Department of Emergency Medicine, University of Michigan, Ann Arbor, MI, USA

2. Department of Family Medicine, University of Michigan, Ann Arbor, MI, USA

3. Department of Emergency Medicine, Los Angeles Biomedical Research Institute, David Geffen School of Medicine at UCLA, Harbor–UCLA Medical Center, Torrance, CA, USA

4. Berry Consultants, Austin, TX, USA

5. Department of Neurology, University of Michigan, Ann Arbor, MI, USA

Abstract

Background: Adaptive clinical trials use accumulating data from enrolled subjects to alter trial conduct in pre-specified ways based on quantitative decision rules. In this research, we sought to characterize the perspectives of key stakeholders during the development process of confirmatory-phase adaptive clinical trials within an emergency clinical trials network and to build a model to guide future development of adaptive clinical trials. Methods: We used an ethnographic, qualitative approach to evaluate key stakeholders’ views about the adaptive clinical trial development process. Stakeholders participated in a series of multidisciplinary meetings during the development of five adaptive clinical trials and completed a Strengths–Weaknesses–Opportunities–Threats questionnaire. In the analysis, we elucidated overarching themes across the stakeholders’ responses to develop a conceptual model. Results: Four major overarching themes emerged during the analysis of stakeholders’ responses to questioning: the perceived statistical complexity of adaptive clinical trials and the roles of collaboration, communication, and time during the development process. Frequent and open communication and collaboration were viewed by stakeholders as critical during the development process, as were the careful management of time and logistical issues related to the complexity of planning adaptive clinical trials. Conclusion: The Adaptive Design Development Model illustrates how statistical complexity, time, communication, and collaboration are moderating factors in the adaptive design development process. The intensity and iterative nature of this process underscores the need for funding mechanisms for the development of novel trial proposals in academic settings.

Funder

NIH Common Fund and the FDA

Publisher

SAGE Publications

Subject

Pharmacology,General Medicine

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