Population Based Intervention to Prevent Obesity in Kindergartens (TigerKids)

NCT00336128 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30000

Last updated 2022-04-13

No results posted yet for this study

Summary

Behavioral intervention at Kindergarten setting aiming at increased fruit and vegetable consumption, decreased intake of high energy foods, snacks, sweets, increased intake of water/low energy drinks, decreased intake of high energy drinks. Physical activity should be more than 1 hour/day and TV/media consumption less than 1 hour/day.

Main questions are:

Do children differ in intervention and control kindergartens according to their nutrition behaviour? Do children in the intervention kindergartens have a higher physical training than such in the control kindergartens? Data were collected with a standardised questionnaire.

Do children differ in intervention and control kindergartens according to their body mass index?

Conditions

Interventions

BEHAVIORAL

attitude change

TigerKids: setting based prevention program to reduce obesity risk factors in children

BEHAVIORAL

adiposity prevention program

The behavioral intervention aimed at modifying physical activity and food and drink choices at the kindergarten setting

Sponsors & Collaborators

  • Child Health Foundation

    collaborator OTHER
  • Bavarian State Ministry of Environment, Public Health and Consumer Protection

    collaborator OTHER_GOV
  • Bavarian Health and Food Safety Authority (LGL)

    collaborator UNKNOWN
  • Institute for Social Paediatrics and Adolescent Medicine, Munich

    collaborator UNKNOWN
  • State Institute of Early Childhood Research, Munich

    collaborator UNKNOWN
  • AOK.Die Gesundheitskasse

    collaborator INDUSTRY
  • Research Centre for Physical Education and Sports of Children and Adolescents, Karlsruhe

    collaborator UNKNOWN
  • Ludwig-Maximilians - University of Munich

    lead OTHER

Principal Investigators

  • Berthold Koletzko, Prof. · Ludwig-Maximilians-Universitaet

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
3 Years
Max Age
7 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2003-10-31
Primary Completion
2006-05-31
Completion
2009-07-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00336128 on ClinicalTrials.gov