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A School-based Education Programme to Reduce Salt Intake in Children and Their Families

A School-based Education Programme to Reduce Salt Intake in Children and Their Families (School-EduSalt)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01821144
Acronym
School-EduSalt
Enrollment
832
Registered
2013-03-29
Start date
2013-03-31
Completion date
2014-02-28
Last updated
2023-01-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy Volunteer

Keywords

dietary salt, 24 hour urinary sodium, blood pressure

Brief summary

The study is to test whether an education programme targeted at school children can lower salt intake in children and their families. In this study, the investigators will educate children on how to reduce salt intake, and the investigators will empower children by asking them to deliver the salt reduction message home to their families, particularly children need to persuade the person who does the cooking for the whole family to cut down on the amount of salt used during food preparations. The study will involve children aged about 11 years, and their parents and grandparents in Northern China.

Interventions

BEHAVIORALSalt reduction

Salt reduction

OTHERControl

No salt awareness education

Sponsors

The George Institute for Global Health, China
CollaboratorOTHER
Peking University
CollaboratorOTHER
Changzhi Medical College
CollaboratorOTHER
Queen Mary University of London
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
9 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Children Inclusion Criteria: * All children in Grade 5 of primary schools (age about 11 years) are eligible for the study.

Exclusion criteria

* Children who do not have lunch or dinner at their own home will be excluded. Adult family members: Inclusion Criteria: * For each participating child, we will recruit two adult family members. All adult family members who share the same meals with the child are eligible for the study.

Design outcomes

Primary

MeasureTime frameDescription
24-h urinary sodium4.5 monthDifference between the intervention and control group in the change in 24-h urinary sodium from baseline to the end of follow-up for children and for adults

Secondary

MeasureTime frameDescription
Blood pressure4.5 monthDifference between the intervention and control group in the change in blood pressure from baseline to the end of follow-up for children and for adults.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026