Design and Application of Airborne Visual Real-time Evaluation System for Air Medical Rescue

This study intends to use AR (Augmented Reality) smart wearing equipment combined with 4G + satellite information transmission system to achieve two-way real-time information transmission in air-to-ground medical rescue.

Study Overview

Detailed Description

Investigators are going to add a pair of wearable smart glasses with AR function to the original flight helmet .During the rescue, the doctors are asked to wear the special helmet, through the device's camera system and headset, investigators can obtain graphics and sound of the helicopter cabin .At the same time, it also receives the historical data of patients and real-time diagnosis as well as rescue guidance from the ground medical institutions.

In short ,it can not only transmit the patient's information in the cabin to the ground medical institutions in real time, but also transmit the rescue plan of the ground medical experts to the rescue helicopter in real time to ensure the safety of patients in transit ,which will save the time for medical staff to hand over after landing and reduce errors.

At present, most of the airborne information exchange systems in air medical rescue in China focus on the internal use of the army, which are incompatible with the medical information systems of most hospitals on the ground. Moreover, these systems can only achieve limited information transmission, and can not delivery rescue scene images in real time. Civil air medical rescue conditions are relatively backward, most of them rely on 2G/3G/4G mobile communication technology, which can lead to failure in case of bad weather or sudden major disasters, and bring great security risks to patients in air medical rescue.

If the airborne visual real-time evaluation system can be successfully completed, it will be popularized and applied in Chinese airborne first aid alliance, and eventually a standardized airborne medical rescue information management system will be formed. Furthermore, a three-dimensional rescue system for civil airborne medical rescue will be built to reduce the potential safety hazards of patients in airborne medical rescue, and to enhance the rapid response ability and organization of medical institutions.

Study Type

Interventional

Enrollment (Anticipated)

100

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Zhejiang
      • Hangzhou, Zhejiang, China, 310000
        • Recruiting
        • Second Affiliated Hospital, School of Medicine, Zhejiang University
        • Contact:
          • Xiuqin Feng
          • Phone Number: 13757119151

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Critically ill patients who require air transportation support;
  • Patients informed consent and sign the informed consent form

Exclusion Criteria:

  • None

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Health Services Research
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: experimental group
During the rescue, the doctor is asked to wear the special helmet , through the device's camera system and headset, we can obtain graphics and sound of the helicopter cabin .At the same time, it also receives the historical data of patients and real-time diagnosis as well as rescue guidance from the ground medical institutions.Patients can receive timely diagnosis and appropriate treatment

We are going to add a pair of wearable smart glasses with AR function to the original flight helmet .During the rescue, the doctor is asked to wear the special helmet , through the device's camera system and headset, we can obtain graphics and sound of the helicopter cabin .At the same time, it also receives the historical data of patients and real-time diagnosis as well as rescue guidance from the ground medical institutions.

It can not only transmit the patient's information in the cabin to the ground medical institutions in real time, but also transmit the rescue plan of the ground medical experts to the rescue helicopter in real time to ensure the safety of patients in transit ,which will save the time for medical staff to hand over after landing and reduce errors.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
percentage of data correctly transmitted
Time Frame: each rescue, for 1 year
Record the data sent from the ground hospital or helicopter cabin and data received in the helicopter cabin or ground hospital. Calculate the percentage of correctly transmitted data.
each rescue, for 1 year
Time-consuming
Time Frame: each rescue, for 1 year
The time required for data transmission
each rescue, for 1 year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Satisfaction index
Time Frame: each rescue, for 1 year
Design a questionnaire to evaluate the satisfaction of using the device by doctors and nurses. The questionnaire consists five items rating from 1 to 5. 1 represents extremely not satisfied, 5 represents very satisfied. The highest score is 25.
each rescue, for 1 year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 5, 2018

Primary Completion (Anticipated)

October 31, 2021

Study Completion (Anticipated)

December 31, 2021

Study Registration Dates

First Submitted

May 16, 2019

First Submitted That Met QC Criteria

May 19, 2019

First Posted (Actual)

May 22, 2019

Study Record Updates

Last Update Posted (Actual)

May 29, 2019

Last Update Submitted That Met QC Criteria

May 24, 2019

Last Verified

May 1, 2019

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • I2018001352

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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