Prevention of Overweight in Infancy (POInz)

July 6, 2020 updated by: Barry Taylor, University of Otago

Primary Prevention of Rapid Weight Gain in Early Childhood: a Randomised Controlled Trial

Obesity is one of the biggest threats to health in the 21st century. Rapid weight gain in the first year of life tends to lead to overweight in children, which in turn leads to overweight in adults. This rapid early weight gain occurs most often at weaning when eating patterns emerge. Infant sleep problems also appear to be associated with the risk of becoming overweight, and contribute to maternal post-natal depression. We propose to undertake a 4-arm randomised controlled trial to determine whether extra education and support for families around weaning and development of early food and activity habits, with or without intervention to improve infant sleep, will decrease the current risk patterns of rapid excessive early childhood weight gain in New Zealand. This would provide strong evidence for the value of such a strategy in the long term control of the obesity epidemic and its consequent complications.

This is a two-year intervention with follow-ups at 3.5, 5 and 11 years of age.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

We plan on undertaking a 4-arm randomised controlled trial to test the following hypotheses:

  1. That anticipatory guidance and extra education and support in infancy around weaning and decreasing/avoiding television watching will delay the timing of introduction of solid foods, will be associated with more successful introduction of nutrient dense foods with appropriate portion size and decrease small screen exposure leading to a lower number of children with excessive weight velocity in infancy and early childhood.
  2. That anticipatory guidance, education and extra support around the early development of infant sleeping patterns will decrease sleep problems, increase infant sleeping time, decrease arousals at night and lower sleep latency which will in turn influence rate of early infant weight gain.
  3. That interventions 1 and 2 will interact additively with regard to infant and early childhood weight gain.
  4. That intervention 2 will lead to lower rates of maternal depression and increased family well being.

Study Type

Interventional

Enrollment (Actual)

802

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • South Island
      • Dunedin, South Island, New Zealand, 9013
        • University of Otago

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

16 years to 55 years (Child, Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Mothers booked for delivery in Dunedin, New Zealand

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 Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
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
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.
Experimental: Sleep
Prevention of sleep problems in first 6 months and then active early intervention for sleep problems from 6 months to 24 months
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.
Experimental: FAB + Sleep
combination of interventions used in arms 2 and 3
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.
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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
BMI z score
Time Frame: 24 months (end of intervention)
BMI z score derived from ht and weight and using World Health Organisation (WHO) growth standards
24 months (end of intervention)
BMI z score
Time Frame: 60 months of age (followup at 5 years of age)
BMI z score derived from ht and weight and using WHO growth standards
60 months of age (followup at 5 years of age)
BMI z score
Time Frame: Follow-up at 11 years of age
BMI z score derived from height and weight and using WHO reference data
Follow-up at 11 years of age

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Dietary intake
Time Frame: 24 months (end of intervention) and 60 months (end of follow-up) and 11 years (further follow-up)
Dietary information (foods, food groups, nutrients) via food frequency questionnaire
24 months (end of intervention) and 60 months (end of follow-up) and 11 years (further follow-up)
Television viewing
Time Frame: 24 months (end of intervention) and 60 months (end of follow-up)
Hours of screen use by parental questionnaire
24 months (end of intervention) and 60 months (end of follow-up)
Major/ Moderate sleep problems
Time Frame: 24 months (end of intervention)
Parents indicate presence of sleep problems in child
24 months (end of intervention)
Physical activity (PA)
Time Frame: 24 months (end of intervention) and 60 months (end of follow-up) and 11 years (further follow-up)
PA measured using actical accelerometry over 5-7 days
24 months (end of intervention) and 60 months (end of follow-up) and 11 years (further follow-up)
Duration of exclusive and any breast feeding
Time Frame: 24 months
Measured by repeated questionnaire
24 months
Parental depression score
Time Frame: Measured at multiple timepoints between pregnancy and 24 months (end of intervention) and 60 months (end of follow-up)
Edinburgh Postnatal Depression questionnaire
Measured at multiple timepoints between pregnancy and 24 months (end of intervention) and 60 months (end of follow-up)
Sleep
Time Frame: 24 months (end of intervention) and 60 months (end of follow-up) and 11 years (further follow-up)
Measured by questionnaire and accelerometry at multiple timepoints
24 months (end of intervention) and 60 months (end of follow-up) and 11 years (further follow-up)
Number of night awakenings
Time Frame: 24 months (end of intervention) and 60 months (end of follow-up)
Measured by questionnaire and accelerometry at multiple timepoints
24 months (end of intervention) and 60 months (end of follow-up)
Self-regulation
Time Frame: 42 and 60 months
Measured by questionnaire and laboratory based measures at follow-up only
42 and 60 months
Body composition
Time Frame: 60 months and 11 years (further follow-up)
Measured by dual-energy x-ray absorptiometry at follow-up only
60 months and 11 years (further follow-up)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Barry J Taylor, FRACP, University of Otago
  • Principal Investigator: Rachael Taylor, PhD, University of Otago

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Helpful Links

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

May 1, 2009

Primary Completion (Actual)

April 1, 2016

Study Completion (Actual)

April 1, 2017

Study Registration Dates

First Submitted

May 3, 2009

First Submitted That Met QC Criteria

May 3, 2009

First Posted (Estimate)

May 5, 2009

Study Record Updates

Last Update Posted (Actual)

July 8, 2020

Last Update Submitted That Met QC Criteria

July 6, 2020

Last Verified

July 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • 105891.01.P.NH
  • HRC 08/374 (Other Grant/Funding Number: NZ Health Research Council)

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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