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Trial registered on ANZCTR
Registration number
ACTRN12611001125910
Ethics application status
Approved
Date submitted
26/09/2011
Date registered
27/10/2011
Date last updated
17/07/2014
Type of registration
Retrospectively registered
Titles & IDs
Public title
Follow-up of children whose mothers participated in the DOMINO trial: does fish oil supplementation in pregnancy influence child development at 4 years?
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Scientific title
Does maternal supplementation with n-3 long-chain PUFA in pregnancy influence cognitive development in childhood?
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Secondary ID [1]
273282
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none
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Universal Trial Number (UTN)
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Trial acronym
The DOMInO 4 Study
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
cognitive development
270860
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Condition category
Condition code
Diet and Nutrition
271036
271036
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0
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Other diet and nutrition disorders
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Mental Health
279238
279238
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0
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Studies of normal psychology, cognitive function and behaviour
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
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]
269451
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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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Cognitive Developement, as assessed by the Differential Ability Scales, 2nd Edition (DASII).
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Assessment method [1]
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Timepoint [1]
279693
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4 years corrected age.
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Secondary outcome [1]
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Language developement, as assessed by the CELF P - Clinical Evaluation of Language Fundamentals during Preschool years.
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Assessment method [1]
294229
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Timepoint [1]
294229
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4 years corrected age.
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Eligibility
Key inclusion criteria
Children who were included in the secondary outcome (neurodevelopment at 18months as assessed by the BSIDIII) of the original DOMInO Trial .
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Minimum age
4
Years
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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
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
18/06/2010
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Actual
18/06/2010
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Date of last participant enrolment
Anticipated
25/09/2010
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Actual
25/09/2010
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
709
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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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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]
269932
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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]
268933
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None
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Name [1]
268933
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Address [1]
268933
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Country [1]
268933
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Women's and Children's Health Network
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Ethics committee address [1]
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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]
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Australia
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Date submitted for ethics approval [1]
271899
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Approval date [1]
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25/03/2010
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Ethics approval number [1]
271899
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12/12/2242
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Summary
Brief summary
The primary aim is to determine whether supplementing pregnant women with DHA-rich capsules from 18-21 weeks of prengnacy until delivery will enhance the general cognitive ability of children at 4 years of age. Hypothesis: Children whose mothers took DHA-rich fish oil capsules during the second half of pregnancy will have enhanced cognitive development at 4 years of age compared with children whose mothers consumed a placebo. This will be investigated using psychometric assessments.
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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
33200
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Prof Maria Makrides
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Address
33200
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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
33200
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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
16447
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Australia
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Phone
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+61 8 82045515
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Fax
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+61 8 82046296
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Email
16447
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[email protected]
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Contact person for scientific queries
Name
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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
7375
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Australia
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Phone
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+61 8 81616719
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Fax
7375
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+61 8 82390267
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Email
7375
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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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