Suspended

Community-based Intervention for Monitoring of Salt Intake in Hypertensive Patients

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What is being tested

Education

+ Reformulation

+ Environmental change

BehavioralDevice
Who is being recruted

Cardiovascular Diseases

+ Hypertension

+ Vascular Diseases

From 18 to 70 Years
+8 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Treatment Study

Interventional
Study Start: January 2022
See protocol details

Summary

Principal SponsorMahidol University
Study ContactPITCHAPORN SONUCH
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: January 10, 2022

Actual date on which the first participant was enrolled.

A randomized-controlled trial was conducted in adult 18-70 years old with hypertensive patients (SBP>130 mmHg) in Uthaithani. Participants were randomized to intervention groups (education, reformulation, environmental change and used salt meter) and control group (standard education and treatment). Trial was followed up for 12 weeks. The primary objective was change in 24-hour urinary sodium excretion between groups and secondary objectives was change in systolic and diastolic blood pressure.

Official TitleCommunity-based Intervention for Monitoring of Salt Intake in Hypertensive Patients
NCT05397054
Principal SponsorMahidol University
Study ContactPITCHAPORN SONUCH
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

240 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 18 to 70 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Cardiovascular DiseasesHypertensionVascular Diseases

Criteria

3 inclusion criteria required to participate
Adults 18-70 years of age with hypertension
Systolic blood pressure > 130 mmHg
Provided informed consent to participate in the study
5 exclusion criteria prevent from participating
Participants with end stage kidney disease
History of adjust antihypertensive agents or diuretic within 2 weeks before enrollment
Pregnant or breastfeeding women
Adjustment of any antihypertensive agents during study period
Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
Education, Reformulation, Environmental change, Used salt meter

Group II

Active Comparator
standard treatment with standard education

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Recruiting

Faculty of Medicine, Ramathibodi Hospital, Mahidol University

Bangkok, ThailandOpen Faculty of Medicine, Ramathibodi Hospital, Mahidol University in Google Maps
SuspendedOne Study Center