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Nutrition Education on the Metabolic Syndrome of Subjects Who Are Frequently Eating Out

Survey on Eating Out Behavior and Dietary Structure in Urban Chinese Citizens and the Effect of Nutrition Education

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01804504
Enrollment
78
Registered
2013-03-05
Start date
2013-03-31
Completion date
2013-10-31
Last updated
2013-03-06

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

Conditions

Metabolic Syndrome

Keywords

Metabolic syndrome, Eating out of home, Nutrition education

Brief summary

The project is aimed at investigating the effect of nutrition education on knowledge, attitude and practice (KAP)of subjects who are frequently eating out, and the effect on metabolic parameters.

Detailed description

The project is aimed at investigating the dietary structure and frequencies of eating out via a cross-sectional study, on the basis of which a randomized, parallel controlled trials is to be carried out.The purpose is to evaluate the effect on metabolic parameters. Hypotheses to be tested:Nutrition education has the effect of improving the metabolic parameters of subjects who are frequently eating out.

Interventions

BEHAVIORALNutrition education

The intervention group will be sent out a series of education materials, be arranged to attend lectures(once a month), dietary guidance or nutrition consultation at regular intervals(once every 2 weeks).

Sponsors

Second Military Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
30 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Shanghai urban citizens * Male or female 18 to 25 years of age; * Frequently eat out(eat out 3 or more times per week); * Clinical diagnosis of Metabolic Syndrome(Meet 3 or more Diagnostic criteria); A. Abdominal obesity: waist circumference\>90cm ( M ), and\>85cm( F ); B. Dyslipidemia:triglyceride≥1.7mmol/L; C. HDL-C \< 1.04mmol/L; D. hypertension: blood pressure≥ 130/85mm Hg ( or have been diagnosed hypertension); E. Hyperglycemia : FPG≥6.1mmol/L and ( or ) 2-hour postprandial blood glucose≥7.8mmol/L and ( or ) have been diagnosed with diabetes; * Signed written informed consent ; * Can attend lectures.

Exclusion criteria

* Pregnant woman; * Temporary resident population; * Participating in another clinical trial 6 months before randomization.

Design outcomes

Primary

MeasureTime frameDescription
Change in Body WeightBaseline and 24 weeksWeight was obtained in light clothing to the nearest 0.1kg using a digital scale 8:00am and 10:00am after an overnight fast between.

Secondary

MeasureTime frameDescription
Change in Blood pressureBaseline and 24 weeks
Change in waist circumference, waist hip ratio, waist to heightBaseline and 24 weeksWaist, hip circumference and height was measured using a plastic tape to the nearest 0.1 cm
Change in Waist, abdominal and hip circumference was measured using a plastic tape to the nearest 0.1 cm Change in fasting blood glucoseBaseline and 24 weeks
Change in serum triglyceride, cholesterol, HDL, LDLBaseline and 24 weeks

Countries

China

Outcome results

None listed

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