Actively Recruiting

Phase 1
Age: 18Years +
All Genders
ID06121661

APPRAISE 2.0: Live Trial of the APPRAISE Trauma Decision Support System

Led by Andrew Tomas Reisner · Updated on 2025-05-08

20

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the APPRAISE trauma decision-support software system to understand how well it works in real-time clinical settings for patients with wounds and injuries. This pilot study aims to assess if the software meets technical performance standards during emergency care and whether it distracts or confuses clinicians, potentially affecting patient care. The study also collects initial data to support planning a larger trial to evaluate the software's effectiveness. The study involves using the APPRAISE system as a real-time bedside tool to assist clinicians in managing trauma patients in the Emergency Department's Acute area. The software's use is monitored from patient arrival through protocol completion, which typically lasts about 30 minutes. The system displays information to guide trauma care during this period. Participants will be adult emergency patients with suspected acute injuries triaged to the Acute area. Researchers collect data through software error tracking and clinician surveys regarding the software's impact on patient care. These assessments occur from arrival through the 30-minute protocol. The study monitors safety and potential risks associated with ongoing software use during trauma management.

CONDITIONS

Brief Title

APPRAISE 2.0: Live Trial of the APPRAISE Trauma Decision Support System

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult (age 18 years or older) Emergency Department patient
  • Triaged to the Acute area of the Emergency Department
  • Clinical concern for acute injury based on chief complaint or documented clinical team concern
Not Eligible

You will not qualify if you...

  • Prisoners
  • Patients known to be pregnant by report, exam, or ultrasound
  • Patients wearing an EFIC Opt-Out bracelet
  • Any clinician, patient, or authorized representative concerns about software suitability for the patient

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - Up to a few hours during Emergency Department arrival

Participants are screened for eligibility to participate in the trial.

1 visit (in-person during Emergency Department arrival)

Implementation

Duration - Typically about 30 minutes after protocol initiation

Participants have the APPRAISE Trauma Clinical Decision Support System used in their care to assist clinical decision-making in real time during trauma management.

Continuous use during the protocol period in the Emergency Department

Trial Site Locations

Total: 1 location

1

Massachusetts General Hospital

Boston, Massachusetts, United States, 02460

Actively Recruiting

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Research Team

I

Iain Kehoe

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DEVICE_FEASIBILITY

Number of Arms

1

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