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Trial registered on ANZCTR
Registration number
ACTRN12615000582550
Ethics application status
Approved
Date submitted
6/01/2015
Date registered
3/06/2015
Date last updated
25/11/2019
Date data sharing statement initially provided
25/11/2019
Type of registration
Retrospectively registered
Titles & IDs
Public title
Developing Children Asthma Program (CAP) in promoting health outcomes among school children
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Scientific title
Effect of the Children Asthma Program (CAP) on level of asthma knowledge among school children with asthma and their caregivers
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Secondary ID [1]
285422
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NIL
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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:
Asthma
293175
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Condition category
Condition code
Respiratory
293452
293452
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0
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Asthma
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Public Health
294528
294528
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0
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Health promotion/education
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
The Children Asthma Program will be implemented to provide education activities to promote the prevention of recurrent and management of asthma among the school children. School children will be divided to two groups ( intervention group and control group )
The intervention group they will receive face to face class room learning. Only one session face to face learning will be given to students for 1 hour. Following the face to face learning online mobile learning will be administer for 3 months which will be electronic alternative for hand workbook tool, the frequency and duration of use of the mobile application it will be flexible and according to user prefer to use it during 3 months.
The parents of children will not receive face to face education only we will give them clarifying session about using mobile application and how to using it to help their children in dealing with mobile application
Baseline data will be collected before the intervention one month after intervention and at third month.
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Intervention code [1]
290341
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Prevention
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Intervention code [2]
291196
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Behaviour
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Comparator / control treatment
The control group will met for session delivered one time take one session for both children and parents in the same time for face to face lecture about the asthma and they will take hand workbook will be designed to be colorful, entertaining, educational, and developmentally appropriate as well as diverse in regards to gender, race, and culture. The content of the workbook includes anatomy and physiology of the lungs, management, and prevention of disease.
The control group the school children, they will support through 3-hours information-sharing program. The CAP will be presented asthma content to the parents follow by questions and answer. The Q&A session leading to increase asthma knowledge, logical reasoning abilities for managing acute episodes, use of effective asthma health behaviors, and acceptance of asthma, and an overview of coalition activities will be presented. Presentation will be limit to 90 minutes then the Q & A will take around 60 - 90 minutes. Hands-outs of the content will be provided.
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Control group
Active
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Outcomes
Primary outcome [1]
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1) Level of knowledge on asthma among school children and caregivers using Knowledge of Asthma Survey
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Assessment method [1]
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Timepoint [1]
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Baseline before intervention, 1st month, then third month post intervention.
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Secondary outcome [1]
310698
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School children problems solving and decisions making regarding management of asthma using Reasoning about Asthma Scenarios
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Assessment method [1]
310698
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Timepoint [1]
310698
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Baseline before intervention, 1st month, then third month post intervention.
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Secondary outcome [2]
312174
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School children’s level of acceptance on asthma using Acceptance of Asthma Questionnaire
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Assessment method [2]
312174
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Timepoint [2]
312174
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Baseline before intervention, 1st month, then third month post intervention.
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Secondary outcome [3]
312175
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Behaviour change among school children using Asthma Health Behaviours Survey
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Assessment method [3]
312175
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Timepoint [3]
312175
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Baseline before intervention, 1st month, then third month post intervention.
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Secondary outcome [4]
312176
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Participation in life activities among school children using Participation in Life Activities questions
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Assessment method [4]
312176
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Timepoint [4]
312176
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Baseline before intervention, 1st month, then third month post intervention.
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Secondary outcome [5]
312177
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Incidence rate of recurrent of asthma, measure by check the medical history for the frequency visiting of health care services due to asthma.
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Assessment method [5]
312177
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Timepoint [5]
312177
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Baseline before intervention 1 month, then third month after intervention.
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Secondary outcome [6]
313003
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Lung capacity (peak flow reading).
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Assessment method [6]
313003
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Timepoint [6]
313003
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Baseline before intervention 1 month, then third month after intervention.
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Eligibility
Key inclusion criteria
School children:
1) known case of asthma
2) availability to participate in scheduled classes sessions
3) able to understand and communicate in Malay or English
Family caregiver:
1) being a designated caregiver of school children with asthma
2) able to understand English or Malay
3) willing to attend and participate in the community component
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Minimum age
13
Years
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Maximum age
70
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
School children or caregivers who are unwilling to participate.
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Study design
Purpose of the study
Educational / counselling / training
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Allocation to intervention
Randomised controlled 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
Open (masking not used)
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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
Completed
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Date of first participant enrolment
Anticipated
2/03/2015
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Actual
15/04/2015
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Date of last participant enrolment
Anticipated
31/12/2015
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Actual
5/02/2016
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Date of last data collection
Anticipated
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Actual
27/05/2016
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Sample size
Target
700
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Accrual to date
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Final
340
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Recruitment outside Australia
Country [1]
6383
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Malaysia
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State/province [1]
6383
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Kuala Lumpur
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Funding & Sponsors
Funding source category [1]
290026
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University
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Name [1]
290026
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University of Malaya Research Grant
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Address [1]
290026
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University of Malaya
50603 Kuala Lumpur, Malaysia
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Country [1]
290026
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Malaysia
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Primary sponsor type
Individual
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Name
Dr.Chong Mei Chan
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Address
Department of Nursing Sciences
Faculty of Medicine
University of Malaya
50603 Kuala Lumpur, Malaysia
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Country
Malaysia
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Secondary sponsor category [1]
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None
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Name [1]
288718
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Address [1]
288718
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Country [1]
288718
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
304810
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UMMC
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Ethics committee address [1]
304810
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Kuala Lumpur, Federal Territory of Kuala Lumpur
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Ethics committee country [1]
304810
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Malaysia
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Date submitted for ethics approval [1]
304810
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30/11/2016
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Approval date [1]
304810
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10/03/2017
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Ethics approval number [1]
304810
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2016112-4501
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Summary
Brief summary
A prospective, longitudinal, cluster randomized clinical trial involving two-group , will be used to evaluate the outcome of Children Asthma Program (CAP).
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Trial website
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Trial related presentations / publications
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Public notes
The University of Malaya new policy to register all the health research project under UMMC ethical committee to fulfillment despite the permission taken by Ministry. The nature of this study is educational and training study and not involve any medical intervention to patient, so it can be allowed to get ethical approval retrospective just to register our study in the university database.
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Contacts
Principal investigator
Name
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Dr Chong Mei Chan
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Address
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Department of Nursing Science,
Faculty of Medicine,
University of Malaya,
50603 Kuala Lumpur,
Malaysia.
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Country
51794
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Malaysia
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Phone
51794
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+603-79493675
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Fax
51794
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Email
51794
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[email protected]
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Contact person for public queries
Name
51795
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Chong Mei Chan
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Address
51795
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Department of Nursing Science,
Faculty of Medicine,
University of Malaya,
50603 Kuala Lumpur,
Malaysia.
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Country
51795
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Malaysia
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Phone
51795
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+603-79493675
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Fax
51795
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Email
51795
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[email protected]
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Contact person for scientific queries
Name
51796
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Chong Mei Chan
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Address
51796
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Department of Nursing Science,
Faculty of Medicine,
University of Malaya,
50603 Kuala Lumpur,
Malaysia.
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Country
51796
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Malaysia
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Phone
51796
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+603-79493675
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Fax
51796
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Email
51796
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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
5852
Ethical approval
367184-(Uploaded-21-11-2019-18-21-07)-Study-related document.jpeg
5853
Informed consent form
[email protected]
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.
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