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Clinical Trials/NCT03396328
NCT03396328CompletedNot Applicable

Effects of Intensive Low-Salt Diet Education by Mobile Application on Albuminuria

Yonsei University1 site in 1 country108 target enrollmentStarted: May 10, 2018Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
108
Locations
1
Primary Endpoint
Decrements of 24-hour urine albumin levels

Study Overview

Brief Summary

Albuminuria is a known risk factor for cardiovascular disease (CVD), chronic kidney disease (CKD) progression, all cause mortality. Inhibition of the renin-angiotension-aldosterone system (RAAS) plays an important role in the reduction of albuminuria and preservation of renal function in patients with CKD and it is known that the daily intakes of sodium have a significant effect on the activity of RAAS. Dietary sodium restriction has been shown to enhances the blood pressure, albuminuria, and renal function preservation. Furthermore, recent study has shown that intensive low-salt dietary education reduces albuminuria in patients with CKD. The average sodium intake of Koreans is 4,791 mg/d, which is higher than other countries. It is difficult for medical staff in Korea to invest enough time in low salt diet.

Recently, the development of health-related applications (apps) has been carried out worldwidely, and researches on lifestyle improvement using apps have been actively studied. However, there is no research yet on whether intensive education using an apps can affect lifestyle habits and thus changes in actual new features. Smartphone apps may provide an alternative to resource-intensive low salt diet-education. Therefore, this study aims to investigate the effect of intensive low salt diet training on the changes of albuminuria using application.

Detailed Description

This is an pen-label, case-control, randomized clinical trial.

  • Run-in period (8 weeks) : before 8 weeks of study initiation, all of the patients have to stop all RAAS blockers or diuretics and switch to antihypertensive agents of other categories such as calcium channel blockers.
  • 0-8 weeks : After run-in period, the patients complete laboratory examination and a dish frequency questionnaire. From 0 weeks, all participants will be prescribed valsartan 80mg per day until the end of study.
  • 8-16 weeks : After 8 weeks, the patients will be randomly assigned to receive an low-salt dietary intervention after second laboratory examination.

Usual education : Conventional education at an outpatient clinic Intensive education : Low salt diet education through Smartphone app

The patients in the conventional education group will receive routine CKD education once at an outpatient clinic. Otherwise, the patients in the intensive education group will be trained low salt diet through smartphone app.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
19 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Age : 19-65
  • •Underlying hypertension or antihypertensive medication , or Systolic blood pressure ≧ 140 mmHg or Diastolic blood pressure ≧ 90
  • •Modification of Diet in Renal Disease study (MDRD) eGFR ≧ 30 ml/min per 1.73m2
  • •Random urine albumin-to-creatinine ratio ≧ 30 mg/g
  • •Smartphone ownership

Exclusion Criteria

  • •Age under 18 or over 66
  • •Uncontrolled hypertension (BP>160/110 mmHg)
  • •Pregnancy within 6 months
  • •Serum potasium > 5.5 mEq/L
  • •malignancy
  • •a diagnosis of CVD (cerebral infarction, hemorrhagic infarction, acute myocardial infarction or unstable angina, coronary angioplasty, or coronary artery bypass surgery) within the last 6 months
  • •Contraindication to angiotensin II receptor blocker
  • •life expectancy less than 6 months

Arms & Interventions

Conventional education

Active Comparator

Intervention: conventional low salt education (Behavioral)

Low salt dietary education by smartphone application

Experimental

Intervention: Intensive low salt dietary education by smartphone application (Behavioral)

Outcomes

Primary Outcomes

Decrements of 24-hour urine albumin levels

Time Frame: 12 weeks after low salt diet education start

Decrements of 24-hour urine albumin levels 12 weeks after low salt diet education

Secondary Outcomes

  • Change of blood pressure with a sphygmomanometer(12 weeks after low salt diet education start)
  • Decrements of 24-hour urine sodium(12 weeks after low salt diet education start)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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