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NCT03342092 Clinical Trial

Early Adiposity Rebound Amongst 4-y.o. Children and Overweight Risk Amongst 11-y.o Children : Third Phase of a Cohort Study in Franche-Comté

Childhood Obesity Clinical Trial

— CoOP  

Official title:
Rebond d'adiposité précoce Chez l'Enfant de 4 Ans et Risque de Surpoids Chez l'Enfant de 11 Ans : troisième Temps d'Une Cohorte Franc-comtoise.

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT03342092
Other study ID # API/2013/43
Secondary ID
Status Active, not recruiting
Phase N/A
First received November 7, 2017
Last updated November 9, 2017
Start date September 24, 2014
Est. completion date December 2017

Study information
Verified date November 2017
Source Centre Hospitalier Universitaire de Besancon
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study aims to assess different methods for early adiposity rebound determination at the age of 4/5 years old according to current medical screening criteria in schools, and to assess their prognostic value for obesity amongst 11 years old pre-adolescents according to the known risk factors.

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 868
Est. completion date December 2017
Est. primary completion date December 2017
Accepts healthy volunteers No
Gender All
Age group 4 Years to 11 Years
Eligibility Inclusion Criteria:

- Boys and girls born between 1st July 2003 and 30th June 2004

- Attending school in Haute-Saône

- Enrolled in the 2008 cohort survey

Exclusion Criteria:

- Children whose parents refused to take part in this cohort study.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Questionnaire
Questionnaires distributed to the families 15 days before child's medical consultation + anthropometric measures and data collected from the personal interview with school nurse

Locations
Country Name City State
France CHU de Besançon Besançon

Sponsors (1)
Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Besancon

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Body mass index of 11 years old pre-adolescents Composite outcome based on height and weight month 22
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