- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06796036
Conversational AI in Tactical Casualty Care: Baseline GPT-4o Improves Combat Medic Decision-Making (FieldAI)
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This study investigates the potential of conversational artificial intelligence (AI), specifically GPT-4, to enhance clinical decision-making in Tactical Combat Casualty Care (TCCC) scenarios. The primary objective is to evaluate whether AI support improves the accuracy and efficiency of ventilator management decisions for combat medics in high-pressure environments without compromising their autonomy.
A prospective, randomized, within-subject study design will be employed. Thirty combat medics from the Czech Armed Forces will participate. Each participant will complete 10 simulated TCCC scenarios: five with AI assistance and five without. Scenarios will be matched for complexity and randomized to control for order effects. Participants will use ChatGPT on handheld devices to simulate real-time AI-assisted decision-making.
In scenarios involving AI assistance, medics will query GPT-4 for support in optimizing mechanical ventilator settings based on patient data, including blood gas results, vital signs, and ventilator parameters.
The primary outcome is the accuracy of ventilator settings as categorized into "excellent," "acceptable," or "failing" based on predefined TCCC standards. Secondary outcomes include decision-making speed and participants' perception of AI's utility, measured through post-scenario surveys.
The findings aim to determine the feasibility of integrating large language models (LLMs) into combat medical care to optimize patient outcomes and support medics under combat conditions. The study seeks to advance the understanding of AI's role in military medicine, providing a foundation for future deployment of fine-tuned AI solutions in TCCC and other critical care scenarios.
This study offers a proof-of-concept evaluation of LLM applications in combat casualty care, with the potential to improve decision-making and inform the development of specialized AI tools for military use.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Praha, Czechia, 16209
- Military University Hospital Prague
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Combat medics actively serving in the Czech Armed Forces
- Completion of standardized Tactical Combat Casualty Care training modules and e-learning on ventilator settings and blood gas interpretation
- Successful passing of pre-tests to ensure a uniform baseline knowledge level.
- Willingness to participate and provide informed consent.
- Availability to complete the full study protocol, including 10 simulated scenarios.
Exclusion Criteria:
- Failure to pass the pre-tests or complete TCCC and ventilator management training
- Prior advanced training or professional certification in critical care or mechanical ventilation that could bias results
- Refusal to provide informed consent or inability to commit to the study schedule
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Combat Medic Decision-Making with and without AI Assistance
All participants will complete 10 Tactical Combat Casualty Care scenarios: 5 with AI assistance using GPT-4 for ventilator management and 5 without AI assistance.
The crossover design ensures each participant experiences both conditions.
|
Participants will complete 10 simulated Tactical Combat Casualty Care (TCCC) scenarios, with 5 scenarios conducted using AI assistance (GPT-4) and 5 without AI.
In AI-assisted scenarios, participants will use GPT-4 to query and optimize ventilator settings based on patient data, while non-AI scenarios rely solely on their clinical judgment.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Accuracy of ventilator settings
Time Frame: 1 hour
|
Accuracy of ventilator settings as categorized into "excellent," "acceptable," or "failing" based on predefined TCCC standards. Excellent means 2 points, acceptable 1 point and failing 0 point. |
1 hour
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Perception of artificial intelligence's utility
Time Frame: 1 hour
|
perception of artificial intelligence's utility, measured through post-scenario survey
|
1 hour
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Michal Soták, M.D., Ph.D., Charles University, Czech Republic
Publications and helpful links
General Publications
- Nemeth C, Amos-Binks A, Rule G, Laufersweiler D, Keeney N, Flint I, Pinevich Y, Herasevich V. TCCC Decision Support With Machine Learning Prediction of Hemorrhage Risk, Shock Probability. Mil Med. 2023 Nov 8;188(Suppl 6):659-665. doi: 10.1093/milmed/usad298.
- Preiksaitis C, Ashenburg N, Bunney G, Chu A, Kabeer R, Riley F, Ribeira R, Rose C. The Role of Large Language Models in Transforming Emergency Medicine: Scoping Review. JMIR Med Inform. 2024 May 10;12:e53787. doi: 10.2196/53787.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- FieldAI
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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