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Trial registered on ANZCTR
Registration number
ACTRN12619000731190
Ethics application status
Approved
Date submitted
10/05/2019
Date registered
16/05/2019
Date last updated
27/02/2020
Date data sharing statement initially provided
16/05/2019
Type of registration
Prospectively registered
Titles & IDs
Public title
Omega Kid Study: Investigating the effect of omega-3 fats for behaviour in 3-5 year old children.
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Scientific title
Omega Kid Study: Investigating the effect of omega-3 supplementation for self-regulation in children aged 3-5 years old.
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Secondary ID [1]
297971
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None
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Universal Trial Number (UTN)
U1111-1231-6483
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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:
Self-regulation
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Executive Function
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Condition category
Condition code
Mental Health
310938
310938
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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
Omega-3 supplementation of 1.59g (combined docosahexaenoic acid (DHA) and eicosapentaenoic acid (EPA)) per day for 12 weeks administered in an encapsulated omega-3 powder.
The main marker for adherence to the intervention is the change in omega-3 blood levels. A calendar sheet will be used for parents to track their child's consumption of the powder, and this will be returned at the end of the study.
Dietary intake of omega-3 at baseline will be captured using the Polyunsaturated Fatty Acid Food Frequency Questionnaire.
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Intervention code [1]
314192
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Treatment: Other
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Comparator / control treatment
Placebo control consisting of powder with encapsulated high oleic acid sunflower oil.
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Control group
Placebo
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Outcomes
Primary outcome [1]
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Self-regulation determined by Head, Toes, Knees, Shoulders Task score
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Assessment method [1]
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Timepoint [1]
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Baseline and 12 weeks after intervention commencement
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Primary outcome [2]
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Self-regulation determined by the Child Self-Regulation and Behaviour Questionnaire
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Assessment method [2]
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Timepoint [2]
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Baseline and 12 weeks after intervention commencement
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Secondary outcome [1]
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Executive Function determined by the Go/No-Go task
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Assessment method [1]
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Timepoint [1]
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Baseline and 12 weeks after intervention commencement
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Secondary outcome [2]
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Executive Function determined by the "Mr Ant" Task
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Assessment method [2]
369500
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Timepoint [2]
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Baseline and 12 weeks after intervention commencement
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Secondary outcome [3]
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Executive Function determined by the Behaviour Rating Inventory of Executive Functioning - Preschool Version Questionnaire
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Assessment method [3]
369501
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Timepoint [3]
369501
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Baseline and 12 weeks after intervention commencement
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Secondary outcome [4]
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Electroencephalographic (EEG) recording and subsequent quantification of EEG power in the delta, theta, alpha, and beta frequency bands from each task (eyes-open resting, eyes-closed resting and executive function tasks) will allow measures of nervous system arousal level (from the eyes-closed resting task).
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Assessment method [4]
369502
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Timepoint [4]
369502
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Baseline and 12 weeks after intervention commencement
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Secondary outcome [5]
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Attention Deficit Hyperactivity Disorder (ADHD) symptoms determined by the Conner's Teacher Rating Scale-15
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Assessment method [5]
369507
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Timepoint [5]
369507
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Baseline and 12 weeks after intervention commencement
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Secondary outcome [6]
369508
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"HS-Omega-3 Index" levels using finger prick blood samples
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Assessment method [6]
369508
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Timepoint [6]
369508
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Baseline and 12 weeks after intervention commencement
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Secondary outcome [7]
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Electroencephalographic (EEG) recording and subsequent quantification of EEG power in the delta, theta, alpha, and beta frequency bands from each task (eyes-open resting, eyes-closed resting and executive function tasks) will allow a measure of nervous system activation (difference in EEG in the eyes-open resting compared to eyes-closed resting tasks).
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Assessment method [7]
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Timepoint [7]
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Baseline and 12 weeks after intervention commencement
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Secondary outcome [8]
370373
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Electroencephalographic (EEG) recording and subsequent quantification of EEG power in the delta, theta, alpha, and beta frequency bands from each task (eyes-open resting, eyes-closed resting and executive function tasks) will allow a measure of task related activation by comparing eyes-open EEG with EEG during the "Mr Ant" and the "Go/No-Go" iPad based executive function tasks (giving a measure of change in brain activity associated with doing the executive function tasks).
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Assessment method [8]
370373
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Timepoint [8]
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Baseline and 12 weeks after intervention commencement
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Eligibility
Key inclusion criteria
Children aged 3 to 5 years old.
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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
Individuals outside the specified age range.
Children with allergies to the supplements.
Children with blood clotting disorders.
Children on blood thinning medication.
Children with an upcoming surgical procedure.
Children with a known developmental delay (but not ADHD).
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Study design
Purpose of the study
Treatment
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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)
Allocation is not concealed
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Simple randomisation using a computerised sequence generator
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people receiving the treatment/s
The people administering the treatment/s
The people assessing the outcomes
The people analysing the results/data
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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
As this study is a pilot feasibility trial we will aim to recruit up to 140 children. Allowing for an approximate drop out rate of 30% will result in up to 100 children completing the trial and 50 per group. We anticipate that this will be enough to detect trends in the data, which then can be used for subsequent power calculations for a larger adequately powered clinical trial.
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
29/07/2019
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Actual
23/08/2019
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Date of last participant enrolment
Anticipated
20/09/2019
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Actual
18/09/2019
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Date of last data collection
Anticipated
14/12/2019
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Actual
22/12/2019
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Sample size
Target
140
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Accrual to date
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Final
76
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Recruitment in Australia
Recruitment state(s)
NSW
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Recruitment postcode(s) [1]
26325
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2522 - University Of Wollongong
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Recruitment postcode(s) [2]
26445
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2519 - Balgownie
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Recruitment postcode(s) [3]
26446
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2517 - Woonona
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Recruitment postcode(s) [4]
26448
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2518 - Corrimal
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Recruitment postcode(s) [5]
26449
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2515 - Coledale
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Recruitment postcode(s) [6]
26450
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2516 - Bulli
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Recruitment postcode(s) [7]
26451
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2528 - Warilla
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Recruitment postcode(s) [8]
26452
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2527 - Albion Park Rail
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Recruitment postcode(s) [9]
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2500 - Wollongong
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Recruitment postcode(s) [10]
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2529 - Shellharbour
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Recruitment postcode(s) [11]
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2525 - Figtree
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Recruitment postcode(s) [12]
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2526 - Cordeaux Heights
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Recruitment postcode(s) [13]
26457
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2502 - Cringila
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Recruitment postcode(s) [14]
26458
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2506 - Berkeley
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Recruitment postcode(s) [15]
26459
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2530 - Dapto
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Recruitment postcode(s) [16]
26460
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2505 - Port Kembla
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Recruitment postcode(s) [17]
26461
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2502 - Primbee
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Recruitment postcode(s) [18]
27154
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2541 - Nowra East
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Recruitment postcode(s) [19]
27155
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2540 - Sanctuary Point
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Recruitment postcode(s) [20]
27156
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2535 - Shoalhaven Heads
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Funding & Sponsors
Funding source category [1]
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University
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Name [1]
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University of Wollongong
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Address [1]
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University of Wollongong, Northfields Ave, Wollongong, NSW, 2522
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Country [1]
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Australia
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Funding source category [2]
302729
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Commercial sector/Industry
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Name [2]
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Nu-Mega Ingredients Pty Ltd
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Address [2]
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Level 1, 7 Clunies Ross Court
Brisbane Technology Park
Eight Mile Plains
4113 QLD
Australia
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Country [2]
302729
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Australia
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Primary sponsor type
University
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Name
University of Wollongong
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Address
University of Wollongong, Northfields Ave, Wollongong, NSW, 2522
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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]
302397
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Address [1]
302397
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Country [1]
302397
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
303151
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University of Wollongong Human Research Ethics Committee
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Ethics committee address [1]
303151
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Research Services Office Building 20, Level 1 University of Wollongong, Northfields Ave Wollongong NSW 2522
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Ethics committee country [1]
303151
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Australia
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Date submitted for ethics approval [1]
303151
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16/04/2019
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Approval date [1]
303151
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25/06/2019
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Ethics approval number [1]
303151
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2019/171
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Summary
Brief summary
The aim of the Omega Kid Study is to investigate the effect of omega-3 supplementation on behavioural outcomes such as self-regulation and executive function in preschool aged children. The study is parallel in design and placebo controlled with the intervention period lasting 12 weeks. Assessments will be conducted at baseline and at 12 weeks, after the intervention period. It is hypothesised that children who receive an active omega-3 supplement will show improvements in self-regulation and executive function, when compared to a matched placebo control group.
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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 Mitch Byrne
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Address
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Bld 41 Rm 41.154a Office of the DVC Health & Communities University of Wollongong, Northfields Ave, NSW, 2522, Australia
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Country
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Australia
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Phone
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+61 2 42215310
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Fax
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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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Lauren Roach
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Address
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Bld 41 Rm 41.309B School of Medicine University of Wollongong, Northfields Ave, NSW, 2522, Australia
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Country
92655
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Australia
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Phone
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+61 2 42213535
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Fax
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Email
92655
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[email protected]
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Contact person for scientific queries
Name
92656
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Lauren Roach
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Address
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Bld 41 Rm 41.309B School of Medicine University of Wollongong, Northfields Ave, NSW, 2522, Australia
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Country
92656
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Australia
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Phone
92656
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+61 2 42213535
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Fax
92656
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Email
92656
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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
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
Effect of omega-3 supplementation on self-regulation in typically developing preschool-aged children: Results of the omega kid pilot study-a randomised, double-blind, placebo-controlled trial.
2021
https://dx.doi.org/10.3390/nu13103561
Embase
The feasibility of the "omega kid" study protocol: A double-blind, randomised, placebo-controlled trial investigating the effect of omega-3 supplementation on self-regulation in preschool-aged children.
2021
https://dx.doi.org/10.3390/nu13010213
N.B. These documents automatically identified may not have been verified by the study sponsor.
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