Healthy Children 2021 Study in Childcare Centers (HC2021)

April 27, 2021 updated by: Helena Rafaela Vieira do Rosario, University of Minho

A Cluster Randomized Controlled Trial Evaluating the Effectiveness of a Healthy Lifestyle Program on Childhood Executive Functions

In Portugal, 17.3% of children under 10 years old are overweight and 7.7% are obese. Research has shown the implementation of healthy lifestyle promotion programs and obesity prevention, however "best practices" are far from being defined. Also, the first five years of life are important for the executive functions development, namely memory, inhibition (including self-regulation) and flexibility, which includes creative thinking, thinking "outside of the box", important in problem solving. The importance of social and emotional dimensions, as well as physical health for the development of cognitive health is consensual, as sleep deprivation, low physical activity, unhealthy food may inhibit the proper development of executive functions.

This project aims to evaluate the effectiveness of a healthy lifestyle promotion program on emotional, social and cognitive development and eating habits, sleep and physical activity in children between 12 and 42 months of age.

A cluster randomised trial will be developed and 300 children, from 16 childcare centres will be invited to participate. Half of the childcare centres will be allocated to the control group and the other half to the intervention group. Data collection will occur before randomisation (at baseline) and after intervention. A feasibility study will be undertaken prior to the experimental study, in accordance with internationally accepted procedures.

The investigators intend to implement the concept that the development of executive functions requires the combination of healthy eating, physical activity and sleep.

The project will contribute with evidence-based to the cognitive, social and emotional development in children.

Study Overview

Study Type

Interventional

Enrollment (Actual)

300

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

      • Braga, Portugal, 4704-553
        • University of Minho

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

1 year to 3 years (Child)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Apparently healthy (with no pre-existing conditions) children aged 12-42 months at baseline.

Exclusion Criteria:

  • Children with disability

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: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Experimental group
The education and training of early childhood educators (developed by the researchers) and their intervention on children.
A 24-week cluster randomized trial will be developed, with the childcare being the randomization unit. Training sessions will be conducted for all early childhood educators in the intervention group. The control group will receive the Portuguese "standard" education and at the end of the intervention this group will also receive the initial training given to the intervention group, so that they can later also implement the intervention. At the end of the intervention, all early childhood educators and parents/guardians will have access to the intervention outcomes.
No Intervention: Control group
Receive the standard care.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in cognitive, social and emotional development
Time Frame: 12 months - 42 months
The Bayley Scales of Infant and Toddler Development - III edition identifies the child's developmental competencies across five major developmental domains; identifies deficits in very young children; and determines the need for further in-depth assessment. Raw scores from the cognitive and social-emotional scale, which does not contain separate subtests, can be converted to a scaled score (M=10, SD=3), which can then additionally be converted to a composite score equivalent (M=100, SD=15). Raw scores for cognitive and motor subtests translate to scaled scores based on 10-day increments up to age 5 months 16 days, at which point norms are based on 1-month intervals (e.g., 5 months 16 days to 6 months 15 days, 35 months 16 days to 36 months 15 days). The normative sample for the social-emotional domain is divided into nine age categories (by months: 0-3, 4-5, 6-9, 10-14, 15-18, 19-24, 25-30, and 31-40). Higher values represent a better performance.
12 months - 42 months
Change in dietary intake
Time Frame: 12 months - 42 months
The child's eating habits will be collected using the one-day food record, completed by parents or early childhood educators.
12 months - 42 months
Change in 24-h movement
Time Frame: 12 months - 42 months
Physical activity, sleep and sedentary behavior will be assessed using the Actigraph accelerometer, which will be used for 5 consecutive days (3 days a week and 2 days a weekend).
12 months - 42 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Sociodemographic profile
Time Frame: 12 months - 42 months
Families' profile will be assessed using the Graffar scale, adapted to Portugal. This is an international social classification, used as an indicator of the various welfare levels of a social group. It includes 5 criteria: occupation, level of education, sources of family income, housing comfort and appearance of the neighbourhood. The sum of the points obtained in the classification provides a final score that corresponds to social class, according to the following classification: Class I (5-9 points), Class II (10-13 points), Class III (14-17 points), Class IV (18-21 points) and Class V (22-25 points). The higher the score, the better the sociodemographic profile.
12 months - 42 months
Family lifestyles
Time Frame: 12 months - 42 months
Families' lifestyles will be assessed through the International Physical Activity Questionnaire-short version, which looks at the types of intensity of physical activity and sitting time that people do as part of their daily lives. It's composed by 7 items, open-ended questions surrounding individuals' (parents) last 7-day recall of physical activity.
12 months - 42 months
Change in length and waist circumference
Time Frame: 12 months - 42 months
Length and waist circumference (cm) will be assessed with no clothes nor shoes using standardised procedures.
12 months - 42 months
Change in weight
Time Frame: 12 months - 42 months
Weight (kg) will be assessed with no clothes and no shoes, using standardised procedures.
12 months - 42 months
Change in blood pressure (systolic and diastolic)
Time Frame: 12 months - 42 months
Digitally assessed, using standardized procedures.
12 months - 42 months

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Rafaela Rosário, Dr, University of Minho

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 (Actual)

September 1, 2019

Primary Completion (Actual)

February 1, 2020

Study Completion (Actual)

October 1, 2020

Study Registration Dates

First Submitted

September 3, 2019

First Submitted That Met QC Criteria

September 5, 2019

First Posted (Actual)

September 9, 2019

Study Record Updates

Last Update Posted (Actual)

April 28, 2021

Last Update Submitted That Met QC Criteria

April 27, 2021

Last Verified

April 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • University of Minho

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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