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Effects of Nutritional Counseling Regularity on the Risk of Cardiovascular Diseases

Effects of Nutritional Counseling Regularity on the Risk of Cardiovascular Diseases

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05092087
Enrollment
129
Registered
2021-10-25
Start date
2021-04-21
Completion date
2021-05-31
Last updated
2021-10-25

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

Conditions

Cerebrovascular Disease

Brief summary

This study aims to investigate the frequency of personalized nutrition counseling's effect on individual cardiovascular risk factors. The study collected 110 to 150 cases data, including a regular blood test, blood glucose, blood lipid, liver panel, and inflammatory factors. The enrolled cases were classified into two groups according to the subjects' duration of consultation: those who completed the consultation and subsequent tests in \>24 weeks were in the control group, whereas those who completed the consultation and subsequent tests in \<24 weeks were in the test group. The effectiveness of nutrition consultation toward managing cardiovascular disease risk factors and its correlation with the subjects' frequency of following the consultations was analyzed using the pre- and post-consultation data. It was found that personalized nutrition consultation significantly improved the subjects' risk factors of cardiovascular diseases, and that the treatment group showed a greater improvement than the control group which who require over 24 weeks to complete all consultation sessions.

Detailed description

The most of interventional studies on nutrition consultation have generally emphasized on the extent to which the diet composition can prevent chronic diseases or provide improvement. Although dietitians play an important role in health education for the primary prevention of chronic disease, their individuals dietary consultation results are mostly focused on weight loss and blood glucose control. However, the effectiveness of nutrition consultation on the prevention of chronic diseases, such as hyperlipidemia, hypertension and cardiovascular diseases, has few been studied. The effectiveness of dietary instructions provided to individuals by dietitians in primary health care institutes is yet to be validated with significant evidence. In addition, nutrition consultation methods, processes, and influencing factors on its results are seldom discussed. Therefore, this study aims to investigate the frequency of personalized nutrition counseling's effect on individual cardiovascular risk factors. The study collected1 10 to 150 cases data who aimed to prevent or improve chronic diseases and had completed eight times individualized nutrition consultations from Bon Vivant Health Lifestyle Management Center, and the pre- and post-consultation data, including a regular blood test, blood glucose, blood lipid, liver panel, and inflammatory factors, will be analyzed. Blood were drawn before and after the first and the last time consultation for biochemical tests; blood pressure and body composition was also measured for comparison. The enrolled cases will be classified into two groups according to the subjects' duration of consultation: those who completed the consultation and subsequent tests in \>24 weeks were in the control group, whereas those who completed the consultation and subsequent tests in \<24 weeks were in the test group. The effectiveness of nutrition consultation toward managing cardiovascular disease risk factors and its correlation with the subjects' frequency of following the consultations was analyzed using the pre- and post-consultation data. It was found that personalized nutrition consultation significantly improved the subjects' risk factors of cardiovascular diseases, and that the treatment group showed a greater improvement than the control group which who require over 24 weeks to complete all consultation sessions.

Interventions

BEHAVIORALnutrition counseling

nutrition counseling

Sponsors

Taipei Medical University
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

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

Inclusion criteria

* Age ≧ 20 * Anyone of follow: body mass index \> 24 systolic blood pressure \> 120 mmHg diastolic blood pressure \> 80 mmHg triglyceride \> 150 mg/dL fasting blood glucose \>100 mg/dL

Exclusion criteria

* Age \<20 * pregnant * Mental problem * unable to do the measurement of body composition * incomplete the nutritional counseling program

Design outcomes

Primary

MeasureTime frameDescription
body weightbaseline, pre-interventionbody weight in kilograms
heightbaseline, pre-interventionheight in meters
body mass indexbaseline, pre-interventionbody mass index in kg/m\^2
The concentration of blood globulinbaseline, pre-interventionblood uric acid in mg/dL
body fatbaseline, pre-interventionbody fat in ratio
The concentration of blood triglyceridebaseline, pre-interventionblood triglyceride in mg/dL
The concentration of blood total cholesterolwithin one week after the interventionblood total cholesterol in mg/dL
The concentration of blood low density lipoprotein-cholesterolbaseline, pre-interventionblood blood low density lipoprotein-cholesterol in mg/dL
The concentration of blood high density lipoprotein-cholesterol-cholesterolbaseline, pre-interventionblood high density lipoprotein-cholesterol in mg/dL
The concentration of blood high sensitive C-reactive proteinbaseline, pre-interventionblood high sensitive sensitive C-reactive protein in mg/L
The concentration of blood fasting glucosebaseline, pre-interventionblood fasting glucose in mg/dL
blood HbA1Cbaseline, pre-interventionblood HbA1C in percentage
The concentration of blood insulinbaseline, pre-interventionblood insulin in mg/dL
The activity of blood aspartate aminotransferasebaseline, pre-interventionblood aspartate aminotransferase in U/L
The activity of blood alanine aminotransferasebaseline, pre-interventionblood alanine aminotransferase in U/L
The concentration of blood urinary nitrogen (BUN)baseline, pre-interventionBUN in mg/L
The concentration of blood creatininebaseline, pre-interventionBUN in mg/dL
The concentration of blood uric acidbaseline, pre-interventionblood uric acid in mg/dL
The concentration of blood total proteinbaseline, pre-interventionblood uric acid in mg/dL
The concentration of blood albuminbaseline, pre-interventionblood uric acid in mg/dL

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026