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Assessing Usefulness of Virtual Reality Mobile Application in Flexible Videoscope Airway Training (AURA)

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ClinicalTrials.gov Identifier: NCT03663296
Recruitment Status : Recruiting
First Posted : September 10, 2018
Last Update Posted : September 10, 2018
Sponsor:
Information provided by (Responsible Party):
National University Hospital, Singapore

Brief Summary:

Flexible videoscope orotracheal intubation (FOI) technique is considered an important option in the management of predicted difficult airways. However, it is rarely performed in daily practice. Yet emergency physicians are expected to be able to perform this skill expertly during a crisis scenario. If it is not completed in a timely and proper fashion, the patient will deteriorate rapidly, resulting in morbidity or fatality.

There is a significant learning curve to master this complex psychomotor skill. Providing sufficient training in FOI, particularly hands-on experience in real patients is difficult. Patients with known difficult airway requiring FOI present infrequently to the emergency room. Using patients with normal airway purely for teaching of FOI is ethically controversial. To avoid technical and ethical concerns of training involving real patients, conventional teaching methods incorporate the use of a low-fidelity manikin in replacement. However, the manikin anatomy often lacks the realism of a live human.

The addition of virtual reality technology, in the form of a low-cost mobile application (Airway Ex) into the conventional simulation, may optimize learning by providing an ethical, cost-effective and more realistic modality to acquire the basic skills of FOI. If it is proven to be effective, efforts to integrate virtual reality technology into routine training of such procedures in the ED should be promoted.

We hypothesize that the addition of virtual reality mobile application to conventional training will improve procedural skill dexterity and proficiency and hence, improve learner's satisfaction and confidence in performing FOI.


Condition or disease Intervention/treatment Phase
Education, Medical Other: Airway Ex App Not Applicable

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 40 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Investigator, Outcomes Assessor)
Primary Purpose: Other
Official Title: Assessing Usefulness of Virtual Reality Mobile Application in Flexible Videoscope Airway Training - a Randomised Controlled Trial
Actual Study Start Date : September 1, 2018
Estimated Primary Completion Date : December 1, 2018
Estimated Study Completion Date : December 1, 2018

Arm Intervention/treatment
Experimental: Interventional
Additional 30 minutes of self-directed learning and practice using the mobile application, after conventional training session
Other: Airway Ex App
30 minutes of self-directed learning and practice using the mobile application

No Intervention: Control
Conventional training session which includes didactic teaching and low-fidelity simulation session involving trainer's demonstration, followed by hands-on practice



Primary Outcome Measures :
  1. Time taken for successful intubation [ Time Frame: 5 minutes ]
    time from advancing scope from manikin's mouth to confirmed placement of endotracheal tube through visualisation with videoscope


Secondary Outcome Measures :
  1. Time taken for visualisation of vocal cords [ Time Frame: 1 minute ]
    time from advancing scope from manikin's mouth to first visualisation of vocal cords with videoscope


Other Outcome Measures:
  1. Quality of flexible videoscope manipulation ability [ Time Frame: 5 minutes ]
    By blinded assessor using validated Five-point Global Rating Scale of Fiberoptic Bronchoscope Manipulation Ability. Score of 1 indicates very poor techniques whereas a score of 5 indicates clearly superior techniques.



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Ages Eligible for Study:   21 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • All doctors from Accidental & Emergency Department of National University Hospital, Singapore

Exclusion Criteria:

  • Refusal for consent

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03663296


Contacts
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Contact: Ying Wei Yau +65-6779 5555 ying_wei_yau@nuhs.edu.sg

Locations
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Singapore
National University Hospital, Singapore Recruiting
Singapore, Singapore, 119074
Contact: Ying Wei Yau    +65-6779 5555    ying_wei_yau@nuhs.edu.sg   
Sponsors and Collaborators
National University Hospital, Singapore
Investigators
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Principal Investigator: Ying Wei Yau National University Hospital, Singapore

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Responsible Party: National University Hospital, Singapore
ClinicalTrials.gov Identifier: NCT03663296     History of Changes
Other Study ID Numbers: AURA
First Posted: September 10, 2018    Key Record Dates
Last Update Posted: September 10, 2018
Last Verified: September 2018
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No