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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT00892983




Registration number
NCT00892983
Ethics application status
Date submitted
3/05/2009
Date registered
5/05/2009
Date last updated
8/07/2020

Titles & IDs
Public title
Prevention of Overweight in Infancy
Scientific title
Primary Prevention of Rapid Weight Gain in Early Childhood: a Randomised Controlled Trial
Secondary ID [1] 0 0
HRC 08/374
Secondary ID [2] 0 0
105891.01.P.NH
Universal Trial Number (UTN)
Trial acronym
POInz
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Obesity 0 0
Growth 0 0
Sleep 0 0
Condition category
Condition code
Diet and Nutrition 0 0 0 0
Obesity
Metabolic and Endocrine 0 0 0 0
Other metabolic disorders

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
BEHAVIORAL - FAB
BEHAVIORAL - Sleep

No intervention: Standard well child care - Standard Well Child Care (SWCC) - 8 Core visits at 2-4 weeks, 6 weeks, 3, 5, 8-10 and 15 months, 2 and 3 years.

Experimental: Food Activity Breast feeding support - FAB (Food Activity Breast feeding support) 8 extra parent contacts for augmented education and support around breast feeding, food and activity

Experimental: Sleep - Prevention of sleep problems in first 6 months and then active early intervention for sleep problems from 6 months to 24 months

Experimental: FAB + Sleep - combination of interventions used in arms 2 and 3


BEHAVIORAL: FAB
Standard well child care plus 7 extra parent contacts for augmented education and support around breast feeding, food and activity with 1 before birth and then at 1-2 weeks, and 3, 4, 7, 9, 13, and 18 months post-partum.

BEHAVIORAL: Sleep
Standard well child care plus 2 extra contacts focussed on Sleep with 1 before birth (anticipatory guidance), and sleep problem prevention at 3 weeks. A sleep problem intervention starting at 6 months was possible for those indicating their child had a sleep problem at 6 months of age. Main prevention advice focussed on placing baby to sleep awake, maximising night-day differences and use of sleep place in parents bedroom for first 6 months. Intervention after 6 months uses preferentially a technique called "parental presence", and if this does not fit family a technique called "camping out" and finally, if neither of the first two fit family, controlled crying.

Intervention code [1] 0 0
BEHAVIORAL
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
BMI z score
Timepoint [1] 0 0
24 months (end of intervention)
Primary outcome [2] 0 0
BMI z score
Timepoint [2] 0 0
60 months of age (followup at 5 years of age)
Primary outcome [3] 0 0
BMI z score
Timepoint [3] 0 0
Follow-up at 11 years of age
Secondary outcome [1] 0 0
Dietary intake
Timepoint [1] 0 0
24 months (end of intervention) and 60 months (end of follow-up) and 11 years (further follow-up)
Secondary outcome [2] 0 0
Television viewing
Timepoint [2] 0 0
24 months (end of intervention) and 60 months (end of follow-up)
Secondary outcome [3] 0 0
Major/ Moderate sleep problems
Timepoint [3] 0 0
24 months (end of intervention)
Secondary outcome [4] 0 0
Physical activity (PA)
Timepoint [4] 0 0
24 months (end of intervention) and 60 months (end of follow-up) and 11 years (further follow-up)
Secondary outcome [5] 0 0
Duration of exclusive and any breast feeding
Timepoint [5] 0 0
24 months
Secondary outcome [6] 0 0
Parental depression score
Timepoint [6] 0 0
Measured at multiple timepoints between pregnancy and 24 months (end of intervention) and 60 months (end of follow-up)
Secondary outcome [7] 0 0
Sleep
Timepoint [7] 0 0
24 months (end of intervention) and 60 months (end of follow-up) and 11 years (further follow-up)
Secondary outcome [8] 0 0
Number of night awakenings
Timepoint [8] 0 0
24 months (end of intervention) and 60 months (end of follow-up)
Secondary outcome [9] 0 0
Self-regulation
Timepoint [9] 0 0
42 and 60 months
Secondary outcome [10] 0 0
Body composition
Timepoint [10] 0 0
60 months and 11 years (further follow-up)

Eligibility
Key inclusion criteria
* Mothers booked for delivery in Dunedin, New Zealand
Minimum age
16 Years
Maximum age
55 Years
Sex
Both males and females
Can healthy volunteers participate?
Yes
Key exclusion criteria
* Women booked after 34 weeks gestation,
* Identified congenital abnormality likely to affect feeding and/or growth
* Home address outside of metropolitan Dunedin or Invercargill,
* Families who are likely to shift out of metropolitan Dunedin or Invercargill in the next 2 years.
* Unable to communicate in English or te reo Maori.

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)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?


The people assessing the outcomes
Intervention assignment
Parallel
Other design features
Phase
NA
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
Recruitment outside Australia
Country [1] 0 0
New Zealand
State/province [1] 0 0
South Island

Funding & Sponsors
Primary sponsor type
Other
Name
University of Otago
Address
Country
Other collaborator category [1] 0 0
Other
Name [1] 0 0
Health Research Council of NZ
Address [1] 0 0
Country [1] 0 0

Ethics approval
Ethics application status

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

Contacts
Principal investigator
Name 0 0
Barry J Taylor, FRACP
Address 0 0
University of Otago
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries

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

TypeCitations or Other Details
Journal Taylor BJ, Gray AR, Galland BC, Heath AM, Lawrence... [More Details]