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Intervention trial for determining recommendation effects of explaining detailed information regarding future cardiovascular risks on rate of visiting medical facilities for those who were found to have chronic diseases in medical check-up

Intervention trial for determining recommendation effects of explaining detailed information regarding future cardiovascular risks on rate of visiting medical facilities for those who were found to have chronic diseases in medical check-up - Next 10

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000024692
Enrollment
6000
Registered
2016-12-01
Start date
2016-12-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Noncommunicable Diseases

Interventions

(a) Selection of examinees who fit the selection policy for research subjects. (b) In addition to the usual notification of the results of the medical checkups, send a letter notifying them that they
s result notification slip will be used to recommend medical examinations, as in the past.

Sponsors

Niigata University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) NIPPON DATA: Patients who have "Probability of death from cardiovascular disease within 10 years: 7-15% or more (2) Patients who meet the following conditions according to the comprehensive risk management chart: "Step 1c Determination of the need for referral to a specialist, etc." (a) Hypertension*: Grade II hypertension (systolic blood pressure 160 mmHg) (a) Hypertension*: Grade II hypertension (systolic blood pressure 160 mmHg, or diastolic blood pressure 100 mmHg) (b) Diabetes mellitus: HbA1c 6.5%*, fasting blood glucose 126mg/dL, or anytime blood glucose 200mg/dL) (c) Dyslipidemia: LDL-C 180mg/dL, HDL-C 30mg/dL, fasting TG 500mg/dL, nonHDL-C 210mg/dL, (d) Chronic kidney disease: severe proteinuria (2+ by the paper method), both proteinuria and hematuria positive (1+ by the paper method), eGFR<50mL/min/1.73m2 (60 in patients 40 years old, 40 in patients 70 years old with stable renal function) (e) Obesity: severe obesity (BMI 35)

Exclusion criteria

Exclusion criteria: none

Design outcomes

Primary

MeasureTime frame
Improvement of weight, blood pressure, lipid, and glucose data after 1 year in the following subjects 1. NIPPON DATA: Patients who have a "probability of death from cardiovascular disease within 10 years: 7-15% or more 2. Patients who meet the following conditions based on the comprehensive risk management chart: "Step 1c: Determination of the need for referral to a specialist, etc." (a) Hypertension a. Hypertension*: Grade II hypertension (systolic blood pressure 160 mmHg, or diastolic blood pressure 100 mmHg) b. Diabetes mellitus: HbA1c 6.5%*, fasting blood glucose 126mg/dL, or anytime blood glucose 200mg/dL) c. Dyslipidemia: LDL-C 180mg/dL, HDL-C 30mg/dL, fasting TG 500mg/dL, nonHDL-C 210mg/dL, d. Chronic kidney disease: severe proteinuria (2+ by the paper method), both proteinuria and hematuria positive (1+ by the paper method), eGFR 50mL/min/1.73m2 (60 in patients 40 years old, 40 in patients 70 years old with stable renal function) e. Obesity: severe obesity (BMI 35)

Secondary

MeasureTime frame
Ratio of antihypertensive, antidiabetic, and antidyslipidemic drug use after 1 year

Countries

Japan

Contacts

Public ContactKiminori Kato

Graduate School of Medical and Dental Sciences Niigata University Department of Laboratory Medicine and Clinical Epidemiology for Prevention of Noncommunicable Diseas

kkato48@med.niigata-u.ac.jp+81-25-227-2117

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026