Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12615001075572
Ethics application status
Approved
Date submitted
18/09/2015
Date registered
13/10/2015
Date last updated
5/04/2024
Date data sharing statement initially provided
11/03/2019
Type of registration
Prospectively registered

Titles & IDs
Public title
Investigating the effect of maternal prebiotic fibre supplementation during pregnancy and breastfeeding on the prevention of early childhood allergies.
Scientific title
A randomised, double-blind, placebo-controlled trial to investigate the effects of maternal dietary prebiotic fibre supplementation, from early pregnancy to 6 months lactation, on infant outcomes of immune function and eczema diagnosis.
Secondary ID [1] 287216 0
Nil
Universal Trial Number (UTN)
Trial acronym
SYMBA Study
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Allergic Disease 295810 0
Condition category
Condition code
Inflammatory and Immune System 296072 296072 0 0
Allergies
Oral and Gastrointestinal 296527 296527 0 0
Normal oral and gastrointestinal development and function

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
2 scoops of study powder containing 9g prebiotics (scGOS/IcFOS 9:1 ratio) will be mixed with food or beverage and consumed orally once daily by the participating pregnant women from study entry (18-20 weeks gestation) until 6 months of lactation. Compliance with the intervention will be assessed by questions asked at regular phone calls and appointment visits during the intervention period. The participating women will also be asked to return any unused study powder tins for reweighing as another measure of compliance at the end of the intervention period.
Intervention code [1] 292502 0
Prevention
Comparator / control treatment
2 scoops of study powder containing 8g of maltodextrin powder will be mixed with food or beverage and consumed orally once daily by the participating pregnant women from study entry (18-20 weeks gestation) until 6 months of lactation. Compliance with the intervention will be assessed by questions asked at regular phone calls and appointment visits during the intervention period. The participating women will also be asked to return any unused study powder tins for reweighing as another measure of compliance at the end of the intervention period.
Control group
Placebo

Outcomes
Primary outcome [1] 336038 0
Infant medically diagnosed eczema by 1 year of age. Infant medically diagnosed eczema is defined by typical eczema skin lesions clinically observed by a medical practitioner. Parents report to trial staff if their infant has been diagnosed with eczema by a medical doctor.
Timepoint [1] 336038 0
1 year of age
Secondary outcome [1] 316400 0
In this composite secondary outcome, the development of allergic disease (eczema and/or food allergy) in the infant, will be determined by completion of interview-administered questions and the infant will be examined for signs of allergic disease.
Timepoint [1] 316400 0
At 3, 6 and 12 months of age of the infant.
Secondary outcome [2] 316401 0
In this composite secondary outcome, the child's sensitisation to food and/or aeroallergens will be assessed by allergy skin prick testing (SPT) with histamine and control solutions in accordance with standard clinical methods as outlined in the 2009 ASCIA Skin Prick Testing for the Diagnosis of Allergic Disease: A manual for practitioners.
Timepoint [2] 316401 0
At 12 months of age of the infant.
Secondary outcome [3] 433658 0
Parent reported medically diagnosed asthma.
Timepoint [3] 433658 0
Secondary outcome [4] 433659 0
Parent reported medically diagnosed asthma.
Timepoint [4] 433659 0
Assessed by parent questionnaire at 3 and 5 years of age
Secondary outcome [5] 433660 0
Parent reported medically diagnosed eczema
Timepoint [5] 433660 0
Assessed by parent questionnaire at 3 and 5 years of age
Secondary outcome [6] 433661 0
Parent reported medically diagnosed eczema
Timepoint [6] 433661 0
Assessed by parent questionnaires at 3 and 5 years of age.
Secondary outcome [7] 433662 0
Parent reported symptoms of allergic rhinitis (hay fever).
Timepoint [7] 433662 0
Assessed by parent questionnaires at 3 and 5 years of age.
Secondary outcome [8] 433663 0
Parent reported symptoms of allergic rhinitis (hay fever).
Timepoint [8] 433663 0
Assessed by parent questionnaire at 3 and 5 years of age.

Eligibility
Key inclusion criteria
Pregnant women less than 21 weeks of gestation, whose infants have a first-degree relative (mother, father or sibling) with a history of medically diagnosed allergic disease (asthma, allergic rhinitis, eczema and/or food allergy). Eligibility is not dependent on intent to breastfeed for a given length of time.
Minimum age
18 Years
Maximum age
50 Years
Sex
Females
Can healthy volunteers participate?
Yes
Key exclusion criteria
Maternal smoking during pregnancy.
Women already regularly consuming prebiotic supplement (more than twice a week).
Current maternal diagnosis of lactose intolerance or cows milk allergy or other significant chronic gastrointestinal condition.

Study design
Purpose of the study
Prevention
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Written informed consent will be obtained before participating in an enrolment appointment. Each participating pregnant woman will be assigned a unique study number and randomly allocated (computer generated) into one of two intervention groups.
The allocation will be concealed be central randomisation using a computer system.
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
The randomisation schedule will be computer-generated (varying size of permuted blocks), and stratified by maternal allergy status and body mass index (BMI). The randomisation schedule will be produced by an independent party.
Masking / blinding
Blinded (masking used)
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
Intervention assignment
Parallel
Other design features
Phase
Not Applicable
Type of endpoint/s
Efficacy
Statistical methods / analysis
We can detect differences in aspects of immune function in studies of this size or smaller, including differences in cytokine detection in our previous intervention studies using probiotics in pregnancy. Although no specific sample size calculations were done for the composite primary outcome for this trial, the subgroup of 120 (60 per group) infant blood samples at 6 months of age that will be selected for immunological studies will be sufficient to detect biologically relevant differences in proposed immune outcomes. This is based on our extensive experience with similar populations.
All analyses will be on an intention-to-treat basis.
For the biological analysis: continuous variables (e.g. cytokines) will be compared between groups with linear regression models (transformation of the outcome variable will be employed as required to meet the assumptions of the linear regression model) to allow for adjustment of confounders. Binary variables will be compared using logistic regression to allow for adjustment of relevant prognostic baseline variables and confounding post-randomisation interactions.

For the clinical analysis, the proportion of children with diagnosed allergic disease at 12 months of age will be compared between treatment groups using an identity binomial generalized linear model, adjusting for the pre-specified prognostic stratification variables. Differences in secondary clinical outcomes will be examined in the same way.

Recruitment
Recruitment status
Active, not recruiting
Date of first participant enrolment
Anticipated
27/05/2016
Actual
29/06/2016
Date of last participant enrolment
Anticipated
Actual
18/11/2021
Date of last data collection
Anticipated
30/06/2027
Actual
Sample size
Target
652
Accrual to date
Final
652
Recruitment in Australia
Recruitment state(s)
WA
Recruitment hospital [1] 4134 0
Joondalup Health Campus - Joondalup
Recruitment postcode(s) [1] 10065 0
6027 - Joondalup

Funding & Sponsors
Funding source category [1] 291791 0
Government body
Name [1] 291791 0
Telethon-Perth Children’s Hospital Research Fund Department of Health of Western Australia
Country [1] 291791 0
Australia
Funding source category [2] 293652 0
Government body
Name [2] 293652 0
National Health and Medical Research Council
Country [2] 293652 0
Australia
Funding source category [3] 316244 0
Government body
Name [3] 316244 0
Western Australia Child Health Research Fund Grant
Country [3] 316244 0
Australia
Primary sponsor type
Other
Name
Telethon Kids Institute
Address
100 Roberts Road
Subiaco, 6008
Western Australia
Country
Australia
Secondary sponsor category [1] 290627 0
None
Name [1] 290627 0
Address [1] 290627 0
Country [1] 290627 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 293459 0
Joondalup Health Campus Human Research Ethics Committee
Ethics committee address [1] 293459 0
Ethics committee country [1] 293459 0
Australia
Date submitted for ethics approval [1] 293459 0
05/11/2014
Approval date [1] 293459 0
02/02/2016
Ethics approval number [1] 293459 0
1541r

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 59314 0
Prof Susan Prescott
Address 59314 0
Telethon Kids Institute
100 Roberts Road
Subiaco WA 6008
Country 59314 0
Australia
Phone 59314 0
+61 8 9489 7714
Fax 59314 0
Email 59314 0
[email protected]
Contact person for public queries
Name 59315 0
Debra Palmer
Address 59315 0
Childhood Allergy and Immunology Research, Level 7, Telethon Kids Institute, Perth Children's Hospital, 15 Hospital Ave, Nedlands WA 6009
Country 59315 0
Australia
Phone 59315 0
+61 8 6319 1750
Fax 59315 0
Email 59315 0
[email protected]
Contact person for scientific queries
Name 59316 0
Debra Palmer
Address 59316 0
Childhood Allergy and Immunology Research, Level 7, Telethon Kids Institute, Perth Children's Hospital, 15 Hospital Ave, Nedlands WA 6009
Country 59316 0
Australia
Phone 59316 0
+61 8 6319 1750
Fax 59316 0
Email 59316 0
[email protected]

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
Yes
What data in particular will be shared?
After de-identification, individual participant data underlying published results only.
When will data be available (start and end dates)?
Beginning 6 months and ending 5 years following main results publication.
Available to whom?
Case-by-case basis at the discretion of CIs Susan Prescott and Debra Palmer
Available for what types of analyses?
For IPD meta-analyses
How or where can data be obtained?
Access subject to approvals by CIs Susan Prescott and Debra Palmer


What supporting documents are/will be available?

Doc. No.TypeCitationLinkEmailOther DetailsAttachment
20309Study protocolDebra J. Palmer, Jeffrey Keelan, Johan Garssen, Karen Simmer, Maria C. Jenmalm, Ravisha Srinivasjois, Desiree Silva, Susan L. Prescott. Study protocol for a randomised controlled trial investigating the effects of maternal prebiotic fibre dietary supplementation from mid-pregnancy to six months’ post-partum on child allergic disease outcomes. Nutrients 2022;14(13):2753. https://doi.org/10.3390/nu14132753  
20310Statistical analysis plan    369064-(Uploaded-16-07-2023-13-12-27)-Study-related document.pdf



Results publications and other study-related documents

Documents added manually
No documents have been uploaded by study researchers.

Documents added automatically
SourceTitleYear of PublicationDOI
Dimensions AIMaternal Fiber Dietary Intakes during Pregnancy and Infant Allergic Disease2019https://doi.org/10.3390/nu11081767
EmbaseStudy Protocol for a Randomised Controlled Trial Investigating the Effects of Maternal Prebiotic Fibre Dietary Supplementation from Mid-Pregnancy to Six Months' Post-Partum on Child Allergic Disease Outcomes.2022https://dx.doi.org/10.3390/nu14132753
N.B. These documents automatically identified may not have been verified by the study sponsor.