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NCT04360083 Clinical Trial

Long-term Assessment of Rhône RéPPOP Care for Overweight and Obese Children.

Pediatric Obesity Clinical Trial

— LTR  

Official title:
Long-term Assessment of Rhône RéPPOP Care for Overweight and Obese Children.

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04360083
Other study ID # 69HCL19_0285
Secondary ID 2020-A00787-32
Status Completed
Phase
First received
Last updated
Start date February 15, 2021
Est. completion date December 7, 2021

Study information
Verified date March 2023
Source Hospices Civils de Lyon
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Childhood obesity is a major public health issue since it is a risk factor of adulthood obesity, cardiovascular disease, psychological disorders, and other chronic conditions. RéPPOP is a two year personalized pathway for multidisciplinary care for overweight and obese children, close to patients' homes. Short and medium-term assessments of Rhône RéPPOP care for overweight and obese children show encouraging results. Long-term assessment is needed to confirm these results. The present study aims to assess the long-term efficiency of Rhône RéPPOP care for overweight and obese children by comparing BMI Z-scores at the start and the end of RéPPOP care to the current BMI. This data will be collected through a telephonic questionnaire by the scientific manager. The study's secondary objectives are to evaluate patients and their families' lifestyle changes and to improve RéPPOP practices.

Recruitment information / eligibility
Status Completed
Enrollment 106
Est. completion date December 7, 2021
Est. primary completion date December 7, 2021
Accepts healthy volunteers No
Gender All
Age group 13 Years and older
Eligibility Inclusion Criteria: - All overweight and obese children included in RéPPOP care programs from 01/01/07 to 31/12/10 Exclusion Criteria: - Refusal to respond to the telephonic questionnaire - Subjects who withdraw their consent to participate in the study - Subjects aged under 12 years

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Collected data from Rhône RéPPOP database
BMI Z-scores at the start and the end of RéPPOP care programs.
• telephonic questionnaire
Collected data though the telephonic questionnaire : current declared BMI Z-score.

Locations
Country Name City State
France Hospices civils de Lyon, Endocrino-pediatric service Bron

Sponsors (1)
Lead Sponsor Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Comparison of BMI Z-scores at the start and the end of RéPPOP care programs to the current BMI Z score. Day 0
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