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Trial registered on ANZCTR
Registration number
ACTRN12611001127998
Ethics application status
Approved
Date submitted
26/09/2011
Date registered
27/10/2011
Date last updated
12/05/2017
Type of registration
Retrospectively registered
Titles & IDs
Public title
The 3 and 5 year follow up of children who participated in the DOMInO study: growth and insulin resistance follow-up.
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Scientific title
The 3 and 5 year follow up of children who participated in the DOMInO study: does maternal supplementation with n-3 long-chain PUFA in pregnancy influence child growth and insulin resistance?
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Secondary ID [1]
252219
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none
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Universal Trial Number (UTN)
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Trial acronym
The ChOIR Study
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
growth
257741
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insulin resistance
279046
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Condition category
Condition code
Diet and Nutrition
257915
257915
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0
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Obesity
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
This study is a follow up from the original DOMInO Study: ACTRN12605000569606.
3 x 0.5 DHA rich Tuna Oil Capsules taken daily from 18-21 weeks until birth of child in The DOMInO Study.
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Intervention code [1]
269453
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Prevention
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Comparator / control treatment
0.5g Blended Vegetable Oil Capsules
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Control group
Placebo
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Outcomes
Primary outcome [1]
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The effect of maternal dietary supplementation with n-3 LCPUFA in pregnancy on the percentage body fat in children at 3 and 5 years of age, using Body Mass Index and Bioelectrical impedance analysis.
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Assessment method [1]
279696
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Timepoint [1]
279696
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3 and 5 years
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Secondary outcome [1]
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Insulin sensitivity in children at 3 and 5 years of age by assessing HOMA-IR
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Assessment method [1]
294236
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Timepoint [1]
294236
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3 and 5 years
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Eligibility
Key inclusion criteria
All children from the original DOMInO trial enrolled from the South Australian recruitment sites.
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Minimum age
3
Years
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Maximum age
5
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
nil
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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)
central telephone and mail
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
computer generated balanced variable blocks
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
Phase 4
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Type of endpoint/s
Safety/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
1/03/2009
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Actual
25/03/2009
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Date of last participant enrolment
Anticipated
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Actual
4/10/2013
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Date of last data collection
Anticipated
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Actual
4/10/2013
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Sample size
Target
1619
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Accrual to date
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Final
1531
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Recruitment in Australia
Recruitment state(s)
SA
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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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NH&MRC
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Address [1]
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National Health and Medical Research Council
GPO BOX 1421
CANBERRA ACT 2601
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Country [1]
269933
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Australia
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Primary sponsor type
Government body
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Name
NH&MRC
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Address
National Health and Medical Research Council
GPO BOX 1421
CANBERRA ACT 2601
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Country
Australia
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Secondary sponsor category [1]
268934
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None
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Name [1]
268934
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Address [1]
268934
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Country [1]
268934
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
271900
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Women's and Children's Health Network
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Ethics committee address [1]
271900
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Women's and Children's Hospital 72 King William Rd North Adelaide SA 5006
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Ethics committee country [1]
271900
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Australia
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Date submitted for ethics approval [1]
271900
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Approval date [1]
271900
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15/01/2009
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Ethics approval number [1]
271900
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11/11/2123
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Summary
Brief summary
The primary aim of the study is to determine the effect of maternal dietary supplementation with n-3 LCPUFA in pregnancy on the percentage body fat in children at 3 and 5 years of age. the pathway to obesity begins early in life, and reducing this early accumulation of excess body fat represents an essential strategy for improving health outcomes across the life course.
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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
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Prof Maria Makrides
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Address
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Women's and Children's Health Research Institute
Level 7, CRB Women's and Children's Hospital
72 King William Road
North Adelaide SA 5006
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Country
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Australia
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Phone
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+61 (0)8 8161 6067
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Fax
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+61 (0)8 8239 0267
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Email
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[email protected]
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Contact person for public queries
Name
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Helen Loudis
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Address
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Child Nutrition Research Centre
Flinders Medical Centre
Flinders Drive
BEDFORD PARK SA 5042
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Country
14640
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Australia
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Phone
14640
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+61 8 82045515
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Fax
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+61 8 82046296
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Email
14640
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[email protected]
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Contact person for scientific queries
Name
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Beverly Muhlhausler
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Address
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Waite Campus, The University of Adelaide
PMB 1, GLEN OSMOND, SA 5064
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Country
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Australia
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Phone
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+61 8 8313 0848
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Fax
5568
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+61 8 8303 7135
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Email
5568
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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
Source
Title
Year of Publication
DOI
Embase
DHA supplementation during pregnancy does not reduce BMI or body fat mass in children: Follow-up of the DHA to Optimize Mother Infant Outcome randomized controlled trial.
2016
https://dx.doi.org/10.3945/ajcn.115.126714
N.B. These documents automatically identified may not have been verified by the study sponsor.
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