Dietary Pattern and Metabolic Health Study

August 22, 2020 updated by: Xu Lin, Chinese Academy of Sciences

This is a single-blind, randomized trial. Based on inclusion and exclusion criteria, 253 eligible volunteers, who were 25-60 years old, with overweight/obese and prediabetes are assigned to one of three dietary patterns: healthy Jiangnan, restricted-calorie; Mediterranean, restricted-calorie; or typical Shanghai, restricted-calorie.

The Shanghai Institutes for Biological Sciences of the Chinese Academy of Sciences(CAS) cooperated with Ruijin Hospital to conduct the study which is funded by the CAS. The study' protocol has been approved by the Ethics Committee of Shanghai Institutes for Biological Sciences. The main purpose of this study is to clarify: the efficacy of traditional Jiangnan dietary pattern, Mediterranean dietary pattern and the current Shanghai dietary pattern in improving overweight/obesity, glucose homeostasis, other cardiovascular metabolic risk factors and their main regulatory factors in Chinese.

Study Overview

Detailed Description

Nowadays, the prevalence of type 2 diabetes and its related metabolic diseases is rapidly rising in China. Obesity and early pathoglycemia will increase the risk of diabetes and related cardiovascular diseases severely. Therefore, more effective methods and strategies need to be found to reduce body weight, improve pathoglycemia, and control the development of this high-risk group to type 2 diabetes. As the most popular healthy dietary pattern in the world, the role of Mediterranean diet in the prevention of type 2 diabetes remains unclear. In addition, the protective role of Chinese traditional dietary pattern with lots of plant-based foods in the region of Jiangnan has not been clarified through intervention studies. Therefore, it is urgent to explore the feasibility and effectiveness of traditional Jiangnan diet and Mediterranean diet through dietary intervention studies in Chinese.

The effectiveness of healthy dietary patterns can be further enhanced by limiting dietary intake to achieve weight loss. Recently, the Spainish study found that energy-restricted Mediterranean diet + physical activity + behavioral interventions are more conducive to weight loss in overweight/obesity with prediabetes/type 2 diabetes compared with conventional Mediterranean dietary interventions. The 2019 Diabetes Management Standard of American Diabetes Association re-emphasizes the importance of moderate weight loss for delaying the progression of type 2 diabetes, and recommends that a reduction in dietary intake is 500-750 kcal/day to reach 1-2 pounds per week is suitable. At the same time, the American Clinical Endocrine Society and the American Endocrine Society have also updated the 2019 Comprehensive Management Guide for Type 2 Diabetes. The new guidelines point out that all overweight or obese patients with prediabetes or type 2 diabetes should pay attention to weight loss. And weight loss treatment should include specific lifestyle interventions, including calorie-restricted healthy dietary plan, physical activity and behavioral interventions.

Dietary intervention studies in the past mainly relied on dietary education. However, this study now provides a healthy and reasonable dietary model for the Chinese population through lifestyle intervention to clarify the improvement of cardiovascular metabolic risk such as overweight/obesity, glucose homeostasis, and the scientific basis for establishing a healthy dietary model which is suitable for Chinese population.

Study Type

Interventional

Enrollment (Actual)

253

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Shanghai
      • Shanghai, Shanghai, China, 200031
        • Ruijin hospital; SAIC FAW-Volkswagen Automobile Co

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

25 years to 60 years (ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Age between 25 to 60 years old
  • 24.0 ≤ BMI ≤ 40.0 kg/m2
  • fasting glucose≥5.6 mmol/L

Exclusion Criteria:

  • Diabetes or use of insulin or other hypoglycemic medications
  • Pregnancy or lactation
  • Trying to change body weight in the way
  • Use of antibiotic in the preceding 3 months for 3-serial days
  • Obvious changes of medication in the preceding 3 months
  • History of drug or alcohol abuse or other substance abuse; (Alcohol abuse is defined as regular alcohol consumption > 40 g/day)
  • Any severe liver or renal diseases
  • Severe gastrointestinal diseases
  • Surgical events preceding 1 year (except appendicitis or hernia surgery)
  • Severe cardiovascular or cerebrovascular diseases or phase three hypertension
  • Implantation of heart stent
  • Cancer or receiving radiotherapy and chemotherapy within 5 years
  • Hyperthyroidism or hypothyroidism
  • Suffering from hepatitis B, tuberculosis, AIDS and other infectious diseases
  • Any mental disorders or current use of antidepressants
  • Food contraindications or allergies to foods included in the intervention
  • Cognitive disability
  • Participated in any other clinical studies within 3 months

Study Plan

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

How is the study designed?

Design Details

  • Primary Purpose: PREVENTION
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: QUADRUPLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Traditional Jiangnan diet
Subjects will be supplied with traditional Jiangnan diet and APP-based behavioral modification
traditional Jiangnan diet supplement from Monday to Friday for six months
EXPERIMENTAL: Mediterranean diet
Subjects will be supplied with Mediterranean diet and APP-based behavioral modification
Mediterranean diet supplement from Monday to Friday for six months
EXPERIMENTAL: Current Shanghai diet
Subjects will be supplied with current Shanghai diet and APP-based behavioral modification
current Shanghai diet supplement from Monday to Friday for six months

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Body weight
Time Frame: 6 months
Body weight will be assessed by electronic scale (Seca-882; ScalesGalore) during each visit and Wi-Fi scale at home
6 months
Glucose homeostasis
Time Frame: 6 months
Glucose homeostasis will be assessed by Continuous Glucose Monitoring(FreeStyle Libre)
6 months
Glucose
Time Frame: 6 months
Glucose will be assessed by oral glucose tolerance test
6 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Abdominal fat
Time Frame: 6 months
Abdominal fat will be assessed using Magnetic Resonance Imaging
6 months
Blood pressure
Time Frame: 6 months
Both systolic pressure and diastolic pressure will be assessed using electronic blood pressure monitor (Omron HEM-7000)
6 months
Total cholesterol
Time Frame: 6 months
Total cholesterol will be assessed using an automatic biochemical analyzer
6 months
Triglyceride
Time Frame: 6 months
Triglyceride will be assessed using an automatic biochemical analyzer
6 months
LDL-C
Time Frame: 6 months
LDL-C will be assessed using an automatic biochemical analyzer
6 months
HDL-C
Time Frame: 6 months
HDL-C will be assessed using an automatic biochemical analyzer
6 months
HbA1c
Time Frame: 6 months
HbA1c will be assessed using liquid Chromatograph Mass Spectrometer
6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

March 1, 2019

Primary Completion (ACTUAL)

September 30, 2019

Study Completion (ACTUAL)

September 30, 2019

Study Registration Dates

First Submitted

February 21, 2019

First Submitted That Met QC Criteria

February 26, 2019

First Posted (ACTUAL)

February 27, 2019

Study Record Updates

Last Update Posted (ACTUAL)

August 26, 2020

Last Update Submitted That Met QC Criteria

August 22, 2020

Last Verified

August 1, 2020

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • CAS-HDP-201902

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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