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Trial registered on ANZCTR
Registration number
ACTRN12621000693820
Ethics application status
Approved
Date submitted
22/07/2019
Date registered
7/06/2021
Date last updated
3/09/2021
Date data sharing statement initially provided
7/06/2021
Date results provided
7/06/2021
Type of registration
Retrospectively registered
Titles & IDs
Public title
Do glove balloons decrease dental anxiety in children-A controlled trial
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Scientific title
Do glove balloons reduce dental anxiety in children- A single blind parallel randomized controlled trial
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Secondary ID [1]
296559
0
"NIL known"
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Universal Trial Number (UTN)
U1111-1223-6548
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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:
dental anxiety
310344
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Condition category
Condition code
Mental Health
309074
309074
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0
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Anxiety
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
intervention is glove balloons
to assess the dental anxiety in children aged(6-12)
intervention given by 2nd year dental students
intervention given individually and face to face
intervention given once only
intervention given during the treatment(in waiting area)
2nd year Dental students(3rd person, not part pf the research) were supposed to give the glove balloon to the children.
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Intervention code [1]
312877
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Behaviour
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Comparator / control treatment
The dental anxiety was assessed at two points in control group and this group recieved no intervention
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Control group
Active
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Outcomes
Primary outcome [1]
308059
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MCDAS(f) Questionnaire was used to assess the dental anxiety in both groups pre and post intervention.
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Assessment method [1]
308059
0
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Timepoint [1]
308059
0
The dental anxiety was assessed immediately after the dental procedure
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Secondary outcome [1]
353848
0
nil
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Assessment method [1]
353848
0
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Timepoint [1]
353848
0
nil
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Eligibility
Key inclusion criteria
children age 6 to 12 years
informed consent by the guardian
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Minimum age
6
Years
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Maximum age
12
Years
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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
children who were unwilling
mentally sick
visual impairment
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Study design
Purpose of the study
Prevention
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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)
sealed opaque envelope
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Simple randomisation using coin tossing/flipping
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people administering the treatment/s
The people assessing the outcomes
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Intervention assignment
Parallel
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
SPSS version 17.0 was used and data was entered in 2 parts. Oone comprised of demographic components of participants which include comparison of gender, age and second which was based on the analysis of anticipatory dental anxiety scores.
Maan-Whitney U Test was used to compare dental anxiety scores of both groups.
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
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Actual
15/05/2015
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Date of last participant enrolment
Anticipated
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Actual
12/08/2015
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Date of last data collection
Anticipated
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Actual
14/08/2015
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Sample size
Target
100
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Accrual to date
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Final
100
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Recruitment outside Australia
Country [1]
21703
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Pakistan
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State/province [1]
21703
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islamabad
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Funding & Sponsors
Funding source category [1]
301138
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University
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Name [1]
301138
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Islamic International Dental College
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Address [1]
301138
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Street 41, Sector G-7/4, Islamabad, Pakistan
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Country [1]
301138
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Pakistan
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Primary sponsor type
University
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Name
Islamic International Dental College
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Address
Street 41, Sector G-7/4, Islamabad, Pakistan
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Country
Pakistan
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Secondary sponsor category [1]
300758
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Hospital
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Name [1]
300758
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Islamic International Dental Hospital
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Address [1]
300758
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Street 41, Sector G-7/4, Islamabad, Pakistan
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Country [1]
300758
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Pakistan
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
301887
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Dr Humza bin Saeed,Community Department, IIDC,
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Ethics committee address [1]
301887
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Street 41, Sector G-7/4, Islamabad, Pakistan
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Ethics committee country [1]
301887
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Pakistan
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Date submitted for ethics approval [1]
301887
0
28/04/2015
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Approval date [1]
301887
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14/05/2015
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Ethics approval number [1]
301887
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IIDC/IRC/2015/005/001
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Summary
Brief summary
The purpose of this study was to assess dental anxiety in children and find effectiveness of using glove balloons in reducing dental anxiety among children. Null hypotheses was stated thus: In children ages 6-12 years, provided with glove balloons visiting dental hospitals(IIDC, PIMS) there is no difference in the mean dental anxiety score measured by MCDAS(f) prior to treatment and the mean dental anxiety score of children not given glove balloons.
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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
88442
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A/Prof Dr Humza bin Saeed
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Address
88442
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Associate Professor Community Dentistry
Street 41, Sector G-7/4, Islamabad, Pakistan
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Country
88442
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Pakistan
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Phone
88442
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+923335134590
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Fax
88442
0
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Email
88442
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[email protected]
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Contact person for public queries
Name
88443
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Dr Humza bin Saeed
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Address
88443
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Associate Professor Community Dentistry
Street 41, Sector G-7/4, Islamabad, Pakistan
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Country
88443
0
Pakistan
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Phone
88443
0
+923335134590
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Fax
88443
0
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Email
88443
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[email protected]
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Contact person for scientific queries
Name
88444
0
Dr Humza bin Saeed
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Address
88444
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Associate Professor Community Dentistry
Street 41, Sector G-7/4, Islamabad, Pakistan
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Country
88444
0
Pakistan
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Phone
88444
0
+923335134590
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Fax
88444
0
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Email
88444
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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)?
Yes
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What data in particular will be shared?
Their names, ages, gender, dental anxiety score for both the control and experimental group
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When will data be available (start and end dates)?
data will be available from 2015 only as it was done few years ago
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Available to whom?
Anyone who wishes to acess it
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Available for what types of analyses?
For any type of analyses that you wish to investigate
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How or where can data be obtained?
Access subjects to approval by principal investigator (
[email protected]
)
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What supporting documents are/will be available?
No Supporting Document Provided
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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