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Trial registered on ANZCTR
Registration number
ACTRN12621000371897
Ethics application status
Approved
Date submitted
21/01/2021
Date registered
31/03/2021
Date last updated
2/03/2022
Date data sharing statement initially provided
31/03/2021
Type of registration
Prospectively registered
Titles & IDs
Public title
The Primary Trauma Care Course Impact on Healthcare worker expertise and Patient Outcome in Vietnam
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Scientific title
The Primary Trauma Care Training Course Impact on Healthcare worker expertise and Patient Outcome in Vietnam
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Secondary ID [1]
302835
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None
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Road Trauma
319806
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Condition category
Condition code
Injuries and Accidents
317737
317737
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0
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Other injuries and accidents
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Our intervention is a trauma training course. The course is a combination of a serial lecture and skill station (scenario). Three trauma experts from Hanoi Medical University will run the course. They are also Primary Trauma Care-PTC instructors with more than 10 years of experience. There are 2 parts in PTC course
Part 1 (theory part):There are 11 trauma lectures which last from 30 to 1 hour. These lectures including: airway management, breathing, circulation, chest injuries, abdominal and limb injuries, head and spinal injuries, trauma in children and pregnancy, burn, secondary survey, disaster management will cover wide range of life-threatening cases.
Part 2 (practice part) with seven trauma skill stations which are basic/advance airway, cervical spine and log-roll, chest drains, analgesia, transportation, paediatric trauma, neurological assessment. Each station will last no more than 20 minutes.
All materials such as: lectures, power point slides or scenarios can be downloaded freely at: https://www.primarytraumacare.org/get-involved/download-resources/
In order to avoid to impair hospital activities and keep the number of class in small size. We will divide participant in each hospital into 3 classes, each class will be run in 2 days (follow PTC standard program). One last day will be spent for post-course evaluation. Consequently, it will take one week in each hospital. All healthcare worker in emergency department in 2 provincial hospitals will be invited and the course will be run in the lecture hall of each hospital.
To evaluate the course, we use a Multiple Choice Question (MCQ) test and clinical checklist. The former is used for knowledge assessment and the latter for skill evaluation. The pre-test will be introduced before the first lesson while the post-test will be done immediately after the course finished. All assessment tool will be also available at https://www.primarytraumacare.org/get-involved/download-resources/
We also use the interview questionnaire to interview some key people in each hospital for qualitative assessment of how the trauma system change by our course.
Finally, We also measure the mortality and morbidity of the patient before and after the intervention (within 6 months each) for secondary outcome.
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Intervention code [1]
319114
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Treatment: Other
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Comparator / control treatment
No control group
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
326083
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Health workers' knowledge by comparing the result of MCQ test post vs pre-course. The MCQ test is 20 questions which are designed by international PTC instructors and available at Primary Trauma Care Foundation website.
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Assessment method [1]
326083
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Timepoint [1]
326083
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baseline (pre-intervention) and immediately post-intervention.
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Primary outcome [2]
326084
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Health workers' skill by comparing the result of prepared checklist pre vs post-course. The clinical checklist are designed and updated annually by international PTC instructors and available at Primary Trauma Care Foundation website.
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Assessment method [2]
326084
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Timepoint [2]
326084
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baseline (pre-intervention) and immediately post-intervention.
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Primary outcome [3]
326962
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Health workers' level of confident by comparing the result of confident matrix pre vs post-course. The confident matrix are designed by international PTC instructors and also available at Primary Trauma Care Foundation website.
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Assessment method [3]
326962
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Timepoint [3]
326962
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pre-course and immediately post-course
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Secondary outcome [1]
390081
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Patient morbidity will be assessed by using hospital medical records (at 24 hours) and phone call (at 1 months)
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Assessment method [1]
390081
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Timepoint [1]
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24 hours and 1 months post trauma
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Secondary outcome [2]
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Patient mortality will be assessed by using hospital medical records (at 24 hours) and phone call (at 1 months)
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Assessment method [2]
392158
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Timepoint [2]
392158
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24 hours and 1 month post trauma
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Secondary outcome [3]
393314
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Trauma system change by comparing the result of key members' interview questionnaire. The interview questionnaire had been designed and reviewed by instructor team of Primary Trauma Care Foundation.
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Assessment method [3]
393314
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Timepoint [3]
393314
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pre-course vs 1 month, 6 months and 1 year post-course
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Eligibility
Key inclusion criteria
All Emergency Department staff in Ninhbinh and Thanhhoa hospital
All alive consenting road trauma patients presenting to participating hospitals emergency departments (including patients under 18 year-old)
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Minimum age
No limit
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
Patients who are:
-Dead on arrival
-Patient with minor injuries without any primary care
-Patient or family members refuse consent.
Staff refuse to joint the project
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Study design
Purpose of the study
Educational / counselling / training
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Allocation to intervention
Non-randomised trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
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Who is / are masked / blinded?
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Intervention assignment
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
1/04/2021
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Actual
10/07/2021
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Date of last participant enrolment
Anticipated
31/08/2022
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Actual
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Date of last data collection
Anticipated
30/09/2022
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Actual
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Sample size
Target
98
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Accrual to date
92
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Final
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Recruitment outside Australia
Country [1]
23347
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Viet Nam
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State/province [1]
23347
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Ha noi
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Country [2]
23348
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Viet Nam
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State/province [2]
23348
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Thanh Hoa
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Country [3]
23349
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Viet Nam
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State/province [3]
23349
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Ninh Binh
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Funding & Sponsors
Funding source category [1]
307258
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University
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Name [1]
307258
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University of Tasmania
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Address [1]
307258
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Churchill Ave, Hobart TAS 7005
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Country [1]
307258
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Australia
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Primary sponsor type
Commercial sector/Industry
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Name
Elphinstone Group
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Address
83 Terra Nova Drive
Wynyard Tasmania Australia 7325
PO Box 717, Wynyard TAS 7325
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Country
Australia
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Secondary sponsor category [1]
308673
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None
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Name [1]
308673
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Address [1]
308673
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Country [1]
308673
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
307352
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Tasmania Health and Medical Human Research Ethics Committee (HMHREC)
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Ethics committee address [1]
307352
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301 Sandy Bay Road, Sandy Bay TAS 7005
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Ethics committee country [1]
307352
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Australia
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Date submitted for ethics approval [1]
307352
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05/02/2021
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Approval date [1]
307352
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17/06/2021
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Ethics approval number [1]
307352
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23982
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Summary
Brief summary
In pre-intervention phase which lasts 6 months, we will investigate the fact and feature of all trauma care system in 2 local hospitals (Ninhbinh and Thanhhoa provincial hospital) which are including level of healthcare worker expertise, patient morbidity and mortality. After that in each hospital we will run a one week PTC training course in intervention phase. Finally, in post-intervention phase, we re- investigate all mentioned features and compare it with corresponding information in pre-intervention phase to answer the question : Can PTC improve participant's expertise and patient's outcome?
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
106938
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Prof Mark Nelson
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Address
106938
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Menzies Institute for Medical Research | University of Tasmania Chair of General Practice
School of Medicine | University of Tasmania 17 Liverpool St Hobart TAS 7000
AUSTRALIA
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Country
106938
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Australia
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Phone
106938
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+61 3 6226 4734
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Fax
106938
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Email
106938
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[email protected]
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Contact person for public queries
Name
106939
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Mark Nelson
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Address
106939
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Menzies Institute for Medical Research | University of Tasmania Chair of General Practice
School of Medicine | University of Tasmania 17 Liverpool St Hobart TAS 7000
AUSTRALIA
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Country
106939
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Australia
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Phone
106939
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+61 3 6226 4734
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Fax
106939
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Email
106939
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[email protected]
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Contact person for scientific queries
Name
106940
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Nguyen Ba Tuan
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Address
106940
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Hanoi Medical University
Number 1, Ton That Tung street, Dong Da District, Ha Noi, Viet Nam
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Country
106940
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Viet Nam
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Phone
106940
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+84 936568824
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Fax
106940
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Email
106940
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
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What supporting documents are/will be available?
No Supporting Document Provided
Doc. No.
Type
Citation
Link
Email
Other Details
Attachment
10122
Study protocol
380970-(Uploaded-21-01-2021-15-17-57)-Study-related document.docx
10123
Informed consent form
380970-(Uploaded-25-12-2020-19-30-39)-Study-related document.docx
10124
Informed consent form
380970-(Uploaded-25-12-2020-19-31-05)-Study-related document.docx
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
Download to PDF