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Clinical Trials in Spain / NCT03465657
Enrolling by invitation Observational

Sodium Sources and Sodium Intake in a Representative Sample of Spanish Children

NCT03465657 · tracked via the Priya Life Science Spain tracker
Sponsor
Universidad Complutense de Madrid
Phase
Observational
Started
2013-10-10
Last updated
2018-03-14

Condition(s) studied

Urinary Sodium ExcretionSalt IntakesBody Weight

Study summary

Previous evidence shows that sodium intake in Spanish adult population is over the recommended limits and this high sodium intake is related with difficulties in body weight control and blood pressure control.

The aim of this study is to stablish a direct relationship between salt intake and the health parameters previously mentioned in a representative sample of Spanish schoolchildren between 7-11 years old. The investigators are applying a 3-day dietary records to collect dietary data, and collecting 24-h urine samples in order to analyse biochemical indicators of sodium intake and other nutrients. Anthropometric data are also being recorded and body composition is also analysed using bioimpedance technique.

Eligibility

Sex
ALL
Min age
7 Years
Max age
11 Years
Healthy volunteers
No
Inclusion Criteria: * Age between 7 and 11 years old Exclusion Criteria: * Those who have any clinical problem, which may modify the results of the analysis: metabolic or chronic diseases (liver, kidney, diabetes, hypothesis or hyperkalemia), pharmacological treatment during the 3 months prior to the study with corticosteroids, insulin, diuretics or other drugs that may modify blood pressure figures, surgery or serious infectious diseases in the previous 6 months. * Those who were not in the school when the measures were taken.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Dto. Nutrición y Ciencia de los Alimentos (NUTRYCIAL). Facultad de Farmacia. UCM Madrid Spain

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03465657 on ClinicalTrials.gov ↗ ← All trials in Spain