Longitudinal Measurement of Caloric Compensation and Eating in the Absence of Hunger in French Preschool Children

One Year Change in Caloric Compensation and Eating in the Absence of Hunger in French Preschool Children

Objectives: The aims were to measure one year change in caloric compensation (CC) and eating in the absence of hunger (EAH) in 3 to 6 year-old French children in their regular eating context and to link these change with individual characteristics (adiposity, age, gender) and maternal feeding practices.

Three series of measurements of caloric compensation (CC) and eating in the absence of hunger (EAH) were conducted: at baseline, and 3 (FU3M) and 15 (FU15M) months later. Each serie of measurement was composed of three consecutive weeks an identical lunch was served in four preschool canteens reaching 236 children. The first lunch was a control session. For the CC situation (week 2), thirty minutes before the lunch children were offered a preload (137 kcal). For the EAH situation (week 3), ten minutes after lunch children were exposed to palatable foods (430 kcal). Food intake was measured at the individual level. Maternal eating behaviour and feeding practices were measured by questionnaires. Child's height and weight were measured by a medical doctor.

Study Overview

Status

Completed

Conditions

Study Type

Observational

Enrollment (Actual)

236

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

      • Dijon, France, 21000
        • Centre des Sciences du Goût et de l'Alimentation

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

2 years to 7 years (Child)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

The population was composed of 236 children at inclusion. Among them, 98 participated in the three time of measurements of caloric compensation or eating in the absence of hunger.

Description

Inclusion Criteria:

  • To be registered to the school canteen, to provide parental approval at inclusion and at the FU15M

Exclusion Criteria:

  • Chronic disease or food allergies

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

  • Observational Models: Cohort
  • Time Perspectives: Cross-Sectional

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in caloric compensation in 15 months
Time Frame: one week
To evaluate the change in caloric compensation across time, caloric compensation was measured at baseline, 3 and 15 months after baseline, in the same conditions. At each time point to assess caloric compensation, children were offered a chocolate bun 30 minutes before the lunch. The food intake at lunch was recorded. We calculated if children compensated the chocolate bun, by comparing energy intake at this lunch with energy intake from a control lunch which took place one week before.
one week
Control measurement of energy intake at baseline
Time Frame: One week
We conducted a control lunch and recorded food intake of each child. This measurement was conducted a week before measuring caloric compensation.
One week
Change in eating in the absence of hunger in 15 months
Time Frame: one week.
In order to evaluate the change in eating in the absence of hunger across time, a measurement was conducted at baseline, 3 months and 15 months after baseline. To collect the measurement of eating in the absence of hunger, we offered palatable foods to children 10 minutes after their lunch. We recorded the energy intake from these post-meal foods. At each time point, this measurement was conducted one week after the measurement of caloric compensation.
one week.
Control measurement of energy intake three months after baseline
Time Frame: One week
We conducted a control lunch and recorded food intake of each child. This measurement was conducted a week before measuring caloric compensation.
One week
Control measurement of energy intake fifteen months after baseline
Time Frame: One week
We conducted a control lunch and recorded food intake of each child. This measurement was conducted a week before measuring caloric compensation.
One week

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Maternal feeding practices and eating behavior
Time Frame: one month after inclusion
Using a validated questionnaire, we collected information about maternal feeding practices (Comprehensive Feeding Practices Questionnaire, Musher-Eizenman & Holub, 2007) and eating behaviour (Dutch Eating Behaviour Questionnaire, Van Strien, 1986).
one month after inclusion

Collaborators and Investigators

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

Collaborators

Investigators

  • Principal Investigator: Nicklaus Sophie, phD, Centre des Sciences du Goût et de l'Alimentation

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.

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

February 1, 2011

Primary Completion (Actual)

March 1, 2011

Study Completion (Actual)

June 1, 2012

Study Registration Dates

First Submitted

October 30, 2013

First Submitted That Met QC Criteria

November 12, 2013

First Posted (Estimate)

November 13, 2013

Study Record Updates

Last Update Posted (Estimate)

November 13, 2013

Last Update Submitted That Met QC Criteria

November 12, 2013

Last Verified

November 1, 2013

More Information

Terms related to this study

Other Study ID Numbers

  • HabEat WP31 Follow up
  • INRA WP31 FU
  • WP31.FU. INRA (Other Identifier: INRA)

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

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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