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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.

Studieoversikt

Detaljert beskrivelse

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.

Studietype

Intervensjonell

Registrering (Forventet)

100

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • Zhejiang
      • Hangzhou, Zhejiang, Kina, 310000
        • Rekruttering
        • Second Affiliated Hospital, School of Medicine, Zhejiang University
        • Ta kontakt med:
          • Xiuqin Feng
          • Telefonnummer: 13757119151

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Barn
  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

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

Exclusion Criteria:

  • None

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Helsetjenesteforskning
  • Tildeling: N/A
  • Intervensjonsmodell: Enkeltgruppeoppdrag
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: 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.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
percentage of data correctly transmitted
Tidsramme: 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
Tidsramme: each rescue, for 1 year
The time required for data transmission
each rescue, for 1 year

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Satisfaction index
Tidsramme: 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

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

5. desember 2018

Primær fullføring (Forventet)

31. oktober 2021

Studiet fullført (Forventet)

31. desember 2021

Datoer for studieregistrering

Først innsendt

16. mai 2019

Først innsendt som oppfylte QC-kriteriene

19. mai 2019

Først lagt ut (Faktiske)

22. mai 2019

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

29. mai 2019

Siste oppdatering sendt inn som oppfylte QC-kriteriene

24. mai 2019

Sist bekreftet

1. mai 2019

Mer informasjon

Begreper knyttet til denne studien

Ytterligere relevante MeSH-vilkår

Andre studie-ID-numre

  • I2018001352

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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