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Blood PressureHEALS-childNCT06097884

Healthy School mEAls With Less Salt:an Action to Reduce Salt Intake in School Meals for Children in Rural China

A study testing Main study intervention-Salt substitute and Ancillary study intervention-Meal trays in people with Blood Pressure, run by Peking University.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

This study aims to assess the impact of the HEALS-Child action project on children's health in rural China. The goal of the project is to evaluate the effectiveness, feasibility, safety and cost-effectiveness of two salt reduction strategies: replacing usual salt with salt substitute in school meals, and replacing… Read more about this study

Who is it for?
Ages 6 to 15 yearsHealthy volunteers can take part
Conditions the study is for
Blood Pressure
What is being tested?
Main study intervention-Salt substitute and Ancillary study intervention-Meal trays
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
16,000 participants
Where
No sites listed yet
Study dates
Oct 2023to Jul 2024
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 6 to 15 years
  • All sexes
  • Healthy volunteers accepted
  • Child

Who may be able to join

  • Attend school stably in this academic year, and expect to take no more than one month of leave for the whole academic year; Have lunch at school at least three times a week.

Who cannot join

  • Unable to complete the baseline blood pressure measurement and spot urine collection.

Trial locations and contacts

No sites are listed yet.

Yifang Yuan, MD contact

+8617310387323

yyfjulie@163.com

About this study

Official title: Healthy School mEAls With Less Salt:an Action to Reduce Salt Intake in School Meals for Children in Rural China(HEALS-child)

This study aims to assess the impact of the HEALS-Child action project on children's health in rural China. The goal of the project is to evaluate the effectiveness, feasibility, safety and cost-effectiveness of two salt reduction strategies: replacing usual salt with salt substitute in school meals, and replacing bowls with trays in school cafeteria. The study has two parts: the main study evaluates the salt substitute intervention, and the ancillary study evaluates the tray intervention. In the main study, over 16000 students from around 320 elementary or junior high school in rural China will be cluster-randomized into the two groups: 1. Salt substitute 2.usual salt. The primary outcome in the main study will be the change in systolic blood pressure. In the ancillary study, over 500 students from 10 elementary or junior high school will be cluster-randomized into the two groups: 1. meal trays 2.bowls. The primary outcome in the ancillary study will be the change in spot urine sodium. The interventions will last over 1 years. To evaluate the impact of interventions, 50 students were randomly selected from each school.

Read the detailed description

The HEALS-Child action(Healthy School mEAls With Less Salt:an Action to Reduce Salt Intake in School Meals for Children in Rural China)is a project launched by China Development Research Foundation, aiming to reduce the salt in school meals and improve the nutrition for rural students. The goal of the study is to evaluate the effectiveness, feasibility, safety and cost-effectiveness of two salt reduction strategies: replacing usual salt with salt substitute in school meals, and replacing bowls with trays in school cafeteria. The study has two parts: the main study evaluates the salt substitute intervention, and the ancillary study evaluates the tray intervention.

  1. Main study:
  2. Aims: The aim in the main study is to test if replacing usual salt with the market available salt substitute in school meals could significantly reduce systolic blood pressure among rural school student. The corresponding null hypotheses in the main study is: the mean change from the baseline in systolic blood pressure of the students in schools that are supplied with salt substitute is equal to that in schools that are supplied with usual salt.
  3. Study design: In the main study, over 16000 students from around 320 elementary or junior high school in rural China will be cluster-randomized into the two groups: 1. Salt substitute 2.usual salt. The salt substitute (NaCl 75% and KCl 25%) will be centrally provided. The intervention will last for two semesters(around 10-months). Before starting the intervention, 50 students were randomly selected from each school, and blood pressure, spot urine sodium and potassium and other indicators were measured at baseline. The randomization will be conducted centrally by the study coordinating center at Peking University Clinical Research Institute, after the baseline survey completed. The students will be followed up for blood pressure measurements and urine collection at the end of the first and second semesters after the intervention.
  4. Outcomes: The primary outcome in the main study is the change in systolic blood pressure from baseline to follow-up. The secondary outcomes in the main study includes: The incidence of hypertension, the change in DBP, spot urine potassium, spot urine sodium, incremental cost-effectiveness ratio (ICER).
  5. Power analysis and statistical analysis: On the assumptions of an intraclass correlation of 0.02, the number of clusters of 320 and 50 students in each school, and an α value of 0.05, the study to detect a mean 0.8 mmHg reduction in systolic blood pressure (SD, 10 mm Hg) between the intervention groups would have a power of 94.8%. Linear models adjusted for clustering based on participants with available measures were used to assess continuous outcomes. Generalized linear mixed model were used for analysis of effects on categorical outcomes.
  6. Ethical considerations:

The study will be submitted to and approved by the Peking University IRB, which has the full accreditation from AAHRRP. The study salt substitute is the product available on Chinese market and has been approved manufactured according to the product standards issued by the ministry of health.

  1. Ancillary study:
  2. Aims: The aim in the ancillary study is to test if replacing bowls with trays in school cafeteria could significantly reduce spot urine sodium among rural school student. The corresponding null hypotheses in the ancillary study is: the mean change from the baseline in spot urine sodium of the students in schools that are supplied with meal trays is equal to that in schools that using bowls.
  3. Study design: In the ancillary study, around 500 students from 10 elementary or junior high school in rural China will be cluster-randomized into the two groups: 1. meal trays 2.bowls. The meal trays will be centrally provided. The intervention will last for two semesters (around 10-months). Before starting the intervention, 50 students were randomly selected from each school, spot urine sodium and other indicators were measured at baseline. The randomization will be conducted centrally by the study coordinating center at Peking University Clinical Research Institute, after the baseline survey completed. The students will be followed up for urine collection at the end of the first and second semesters after the intervention.
  4. Outcomes: The primary outcome in the ancillary study is the change in spot urine sodium from baseline to follow-up. The secondary outcomes in the ancillary study includes incremental cost-effectiveness ratio (ICER).
  5. Power analysis and statistical analysis: On the assumptions of an intraclass correlation of 0.02, the number of clusters of 10 and 50 students in each school, and an α value of 0.05, the study to detect a mean 1g reduction in spot urine sodium (SD, 2.15g) between the intervention groups would have a power of 90.0%. Linear models adjusted for clustering based on participants with available measures were used to assess continuous outcomes.
  6. Ethical considerations:

The study will be submitted to and approved by the Peking University IRB, which has the full accreditation from AAHRRP.

Conditions
Blood Pressure
Being tested
Main study intervention-Salt substitute, Main study control-Usual salt, Ancillary study intervention-Meal trays, Ancillary study control-Bowls
Keywords
Salt reduction

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Main study intervention-Salt substituteOther

    replacing regular salt with salt substitute in school meals

  • Main study control-Usual saltOther

    Use usual salt in school meals

  • Ancillary study intervention-Meal traysOther

    Replacing bowls with trays in school cafeteria

  • Ancillary study control-BowlsOther

    Use bowls in school cafeteria

Study groups in NCT06097884
Study groupRoleWhat they receive
Main study intervention- Salt substituteExperimentalReplacing usual salt with salt substitute in school meals
Receives: Other: Main study intervention-Salt substitute
Main study control- Usual saltPlacebo comparatorUsing usual salt in school meals
Receives: Other: Main study control-Usual salt
Ancillary study intervention- Meal trayExperimentalReplacing bowls with trays in school cafeteria
Receives: Other: Ancillary study intervention-Meal trays
Ancillary study control- BowlPlacebo comparatorUsing bowls in school cafeteria
Receives: Other: Ancillary study control-Bowls

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Primary outcome for the main study-Systolic blood pressure

    The change in systolic blood pressure from baseline to follow-up

    Measured: 10-month

  2. Primary outcome for the ancillary study-Spot urinary sodium

    The change in spot urinary sodium from baseline to follow-up

    Measured: 10-month

Secondary outcomes (6)
  1. Secondary outcome for the main study-Incidence of hypertension

    The new-onset hypertension during study period

    Measured: 10-month

  2. Secondary outcome for the main study-Spot urinary sodium

    The change in spot urinary sodium from baseline to follow-up

    Measured: 10-month

  3. Secondary outcome for the main study-Spot urinary potassium

    The change in spot urinary potassium from baseline to follow-up

    Measured: 10-month

  4. Secondary outcome for the main study-Diastolic blood pressure

    The change in diastolic blood pressure from baseline to follow-up

    Measured: 10-month

  5. Secondary outcome for the main study-ICER

    Incremental cost-effectiveness ratio, defined by the difference in the cost for every unit of gain in the pertained effectiveness outcome

    Measured: 10-month

  6. Secondary outcome for the ancillary study-ICER

    Incremental cost-effectiveness ratio, defined by the difference in the cost for every unit of gain in the pertained effectiveness outcome

    Measured: 10-month

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Oct 2023
  2. Study startOct 2023 (estimated)
  3. Primary completionJul 2024 (estimated)
  4. Study completionJul 2024 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
16,000 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06097884
Sponsor's protocol ID
2023157
Acronym
HEALS-child
Status last verified
Sep 2023
First submitted
9 Oct 2023
Last updated
24 Oct 2023
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Main study intervention-Salt substitute and Ancillary study intervention-Meal trays in people with Blood Pressure, run by Peking University.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 24 Oct 2023. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Yifang Yuan, MD (+8617310387323, yyfjulie@163.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Primary outcome for the main study-Systolic blood pressure (time frame: 10-month). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Oct 2023.

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