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Trial registered on ANZCTR
Registration number
ACTRN12609001000291
Ethics application status
Approved
Date submitted
14/10/2009
Date registered
19/11/2009
Date last updated
19/11/2009
Type of registration
Retrospectively registered
Titles & IDs
Public title
Improved dental health for remote Aboriginal children: a cluster randomised trial.
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Scientific title
Among children living in remote communities does a comprehensive primary health care intervention (including fluoride varnish) compared to usual care reduce the incidence of new caries?
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Universal Trial Number (UTN)
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Trial acronym
STLK: Strong Teeth for Little Kids
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Early childhood caries
251998
0
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Condition category
Condition code
Public Health
252191
252191
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0
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Epidemiology
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Oral and Gastrointestinal
252425
252425
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0
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Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
A comprehensive primary health intervention (including fluoride varnish applications every 6 months). The fluoride varnish is applied at baselines and every 6 months for a total of 2 years (5 applications). Other intervention activities also occur every 6 months- these include training of health staff in oral health promotion, identification of caries, and application of fluoride varnish, oral health promotion with individual familes, and oral health promotion with child care centres, preschools, communitiy councils, and stores.
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Intervention code [1]
241409
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Prevention
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Intervention code [2]
241555
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Other interventions
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Comparator / control treatment
Standard care. Usual access to local health clinic and Children's Dental Service for any oral health problems identified over a total period of 2 years.
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Control group
Active
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Outcomes
Primary outcome [1]
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Caries increment (rate of new caries) assessed by dental examination.
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Assessment method [1]
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0
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Timepoint [1]
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2 years from baseline.
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Secondary outcome [1]
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Caries increment (with adjustment of potential confounders) assessed by dental examination.
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Assessment method [1]
257901
0
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Timepoint [1]
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2 years from baseline.
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Secondary outcome [2]
257902
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Gingivitis assessed by dental examination.
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Assessment method [2]
257902
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Timepoint [2]
257902
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2 years from baseline.
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Secondary outcome [3]
257903
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Dental abscess assessed by dental examination.
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Assessment method [3]
257903
0
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Timepoint [3]
257903
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2 years from baseline.
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Secondary outcome [4]
257904
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The proportion of children undergoing a dental procedure (including fluoride varnish application) by dentist or dental therapist assessed by dental examination and review of medical records.
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Assessment method [4]
257904
0
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Timepoint [4]
257904
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2 years from baseline.
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Secondary outcome [5]
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Behavioural change as reported by parents in questionnaires completed at baseline and at 2 year follow up.
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Assessment method [5]
257905
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Timepoint [5]
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2 years from baseline.
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Secondary outcome [6]
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Adverse events- any reaction to fluoride varnish requiring medical review. Reactions resulting in admission to hospital or considered life-threatening will be reported as serious adverse events. These will be assessed by review of medical records.
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Assessment method [6]
257906
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Timepoint [6]
257906
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2 years from baseline.
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Eligibility
Key inclusion criteria
Aboriginal
Aged 18m to 4y
Living in a remote community
Able to attend clinic for regular follow up
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Minimum age
18
Months
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Maximum age
4
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
Allergy to fluoride varnish
Receiving treatment for asthma
Congenital dental disease
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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)
Communities were allocated to intervention or control group. Allocation concealment was achieved by central randomisation by computer.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Allocation sequence computer generated by statistician and concealed from all investigators, study staff and study participants
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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
Parallel
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Other design features
Cluster randomised (by community)
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Phase
Not Applicable
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Type of endpoint/s
Efficacy
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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
1/05/2006
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
700
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
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Funding & Sponsors
Funding source category [1]
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Government body
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Name [1]
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National Health and Medical Research Council
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Address [1]
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GPO Box 1421
Canberra ACT 2601
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Country [1]
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Australia
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Primary sponsor type
University
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Name
Menzies School of Health Research
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Address
PO Box 41096
Darwin NT 0811
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Country
Australia
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Secondary sponsor category [1]
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None
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Name [1]
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Address [1]
251219
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Country [1]
251219
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Other collaborator category [1]
904
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University
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Name [1]
904
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Australian Research Centre for Population Oral Health
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Address [1]
904
0
University of Adelaide
North Terrace
Adelaide, SA 5005
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Country [1]
904
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
243993
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Human Research Committe of the NT Department of Health and Families and the Menzies School of Health Research
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Ethics committee address [1]
243993
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PO Box 41096 Darwin, NT 0811
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Ethics committee country [1]
243993
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Australia
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Date submitted for ethics approval [1]
243993
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Approval date [1]
243993
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16/12/2005
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Ethics approval number [1]
243993
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05/70
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Summary
Brief summary
Dental decay has been described as the most common disease of childhood that is not self-limiting or responsive to short-term pharmacological management. Regrettably, Australian Aboriginal children have, on average, twice as many teeth affected by decay as other Australian children. The disease is a particular burden for pre-school children who do not routinely have access to dental care provided by the state/territory programs. The goal of this project is to develop, implement and evaluate the effectiveness of a community-oriented, primary health care intervention to prevent dental decay among pre-school children in Aboriginal communities in the Northern Territory. The cluster randomized design provides a practical approach to the problem of small numbers of children living in remote communities. The results obtained from this research proposal would make an important contribution to the health care of Australian Aboriginal children and other disadvantaged children throughout the world.
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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
30384
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Address
30384
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Country
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Phone
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Fax
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Email
30384
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Contact person for public queries
Name
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Peter S Morris
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Address
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Menzies School of Health Research
PO Box 41096
Darwin, NT 0811
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Country
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Australia
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Phone
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+61 8 89228196
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Fax
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+61 8 89275187
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Email
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[email protected]
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Contact person for scientific queries
Name
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Peter S Morris
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Address
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Menzies School of Health Research
PO Box 41096
Darwin, NT 0811
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Country
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Australia
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Phone
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+61 8 89228196
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Fax
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+61 8 89275187
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Email
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[email protected]
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No information has been provided regarding IPD availability
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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