NCT02952768

Brief Summary

Ultrasound is a frequently used diagnostic tool in the emergency department and suggested to have a role during resuscitation. The aims of this study were to develop a novel, resuscitative ultrasound-circulation-airway-breathing (US-C-A-B) protocol, to implement a short curriculum and to assess the feasibility. The US-C-A-B protocol was built in an advanced life support-compliant manner. It involved a 3-part assessment: (1) C: subxiphoid 4-chamber view of the heart; (2) A: tracheal ultrasound; and (3) B: bilateral lung sliding. It could be used for direct confirmation for the C-A-B and searching the possible cause of cardiac arrest. A half-day curriculum was designed, and comprised of one-hour didactics and 3-hour small-group hand-on training. Assessments were performed, including a written test, the US image acquisition and a satisfaction survey. From August 1, 2014 to March 31, 2016, the multi-center emergency physicians who attended the US-C-A-B curricula were enrolled prospectively.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Aug 2014

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 1, 2014

Completed
2.2 years until next milestone

First Submitted

Initial submission to the registry

October 26, 2016

Completed
7 days until next milestone

First Posted

Study publicly available on registry

November 2, 2016

Completed
1.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2017

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2017

Completed
Last Updated

February 23, 2017

Status Verified

October 1, 2016

Enrollment Period

3.3 years

First QC Date

October 26, 2016

Last Update Submit

February 21, 2017

Conditions

Outcome Measures

Primary Outcomes (1)

  • The time of the US image acquisition

    The 6-month evaluation was performed in cardiac arrest patients. The ultrasound operation time was from the time to initiate the ultrasound exam to when the sonographers to inteprete the results, using the ultrasound recorder.

    6 months

Secondary Outcomes (3)

  • Learning efficacy was assessed with a written test with 10 multi-choice questions.

    through study completion, an average of 1 year

  • A satisfaction survey with a 5-point Likert scale.

    through study completion, an average of 1 year

  • The time of the US image acquisition

    through study completion, an average of 1 year

Study Arms (1)

ultrasound training

OTHER

The aims were to develop a novel, resuscitative ultrasound-circulation-airway-breathing (US-C-A-B) protocol, to implement a short curriculum for ultrasound training and to assess the feasibility.

Behavioral: ultrasound training

Interventions

Through the ultrasound-circulation-airway-breathing training curriculum to integrate the ultrasound into clinical practice.

ultrasound training

Eligibility Criteria

Age25 Years - 60 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • The enrolled participants were emergency physicians of the National Taiwan University Hospital (NTUH), the Far-Eastern Memorial Hospital (FEMH) and the Chang-Kung Memorial Hospital (CKMH), three teaching hospitals in Taiwan.

You may not qualify if:

  • Not emergency physicians.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

National Taiwan University Hospital

Taipei, Taiwan, 100, Taiwan

RECRUITING

Study Officials

  • Wan-Ching Lien, Ph.D.

    National Taiwan University Hospital

    STUDY DIRECTOR

Central Study Contacts

Wan-Ching Lien, Ph. D.

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
OTHER
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

October 26, 2016

First Posted

November 2, 2016

Study Start

August 1, 2014

Primary Completion

December 1, 2017

Study Completion

December 1, 2017

Last Updated

February 23, 2017

Record last verified: 2016-10

Data Sharing

IPD Sharing
Will not share

Locations