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Developing a Comparative Effective Methodology for Technology Usability During a Simulated Casualty Event.

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This study developed a simulation method to compare combat casualty care technologies. Medics evaluated devices for usability, informing selection and iterative updates for future battlefield medical readiness.

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Area of Science:

  • Military Medicine
  • Biomedical Engineering
  • Human Factors Engineering

Background:

  • Future combat environments present complex challenges for multi-domain battlefield injuries.
  • Technology integration is crucial for enhancing provider capabilities in combat casualty care.
  • Army experimentation exercises evaluate new concepts and technologies for force integration across all domains.

Purpose of the Study:

  • To develop a method for empirically comparing medical devices for combat casualty care.
  • To prepare for an Army experimentation exercise by evaluating technology through high-fidelity simulation.
  • To incorporate end-user (medic) input for user-centered technology design and rapid improvements.

Main Methods:

  • Six medics participated in high-fidelity simulation scenarios involving medical casualty injuries.
  • Technology devices were evaluated with and without their use during simulated care delivery.
  • Usability data was collected using the System Usability Scale and Adapted Telehealth Usability Questionnaire-Telemedicine and Advanced Technology Research Command, alongside qualitative feedback.

Main Results:

  • A comparative effectiveness design assessed devices on usability, size, weight, power, cost, connectivity, and cybersecurity.
  • Qualitative feedback provided a holistic assessment of technologies within the combat casualty care scenario.
  • The methodology holistically assessed technologies applied in the combat casualty care scenario.

Conclusions:

  • Results informed decision-makers on technology inclusion for experimentation exercises and proof-of-concept scaling.
  • Developer feedback facilitated iterative updates for devices prior to experimentation.
  • This project contributes empirical medical technology assessments with end-user input, supporting user-centered design for rapid improvements before fielding.