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Lifestyle Intervention Trial in High Metabolic Risk Chinese

Primary Purpose

Metabolic Syndrome X

Status
Not yet recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Routine education
Programmed smartphone intervention
Programmed smartphone plus dietitian intervention
Sponsored by
Chinese Academy of Sciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Metabolic Syndrome X focused on measuring metabolic risk, lifestyle intervention, homeostasis

Eligibility Criteria

20 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Volunteers at high metabolic risk aged 20-65 who didn't participate in other studies in 3 months before the current research, having a certain level of education and normal cognitive ability, taking good care of himself/herself at least meet three of the following criterions(NCEP- ATPIII, for Asian Americans):

  • Waist circumference ≥90 cm (men), ≥ 80 cm (women).
  • total triglyceride ≥ 1.7 mmol/L.
  • HDL-c <1.03 mmol/L in men, <1.3 mmol/L in women.
  • systolic blood pressure ≥ 130 mmHg or diastolic blood pressure ≥ 85mmHg.
  • Fasting plasma glucose ≥ 5.6 mmol/L.

Exclusion Criteria:

  • Fasting glucose>7.0mmol/L or diagnosed diabetes or taking insulin or other blood glucose-lowering drugs
  • Diagnosed phase three hypertension or can't lowering SBP under 160mmHg after anti-hypertension drugs
  • Fasting blood TG≥ 5.7 mmol/L or fasting LDL-C≥ 4.9 mmol/L or taking lipid-lowering drugs
  • Pregnancy or lactation
  • Obvious drug changing in three months before research
  • History of drug or alcohol abuse or other substance abuse (Alcohol abuse is defined as more than 40 g/day of alcohol for woman, and more than 80g/day for man)
  • Severe kidney and liver diseases (blood biomarkers such as alt, serum creatinine is 1.5 times over the scope of normal setting)
  • Severe Gastrointestinal diseases (such as severe diarrhea, constipation, severe digestive tract inflammation, active peptic ulcer, acute cholecystitis, etc.)
  • Having surgeries within one year before research such as heart stents implanted surgery (expect for appendicitis or hernia operation)
  • Severe cardiovascular disease (e.g., heart failure, myocardial infarction, cerebral infarction, and acute myocarditis, severe arrhythmia, received the intervention therapy, etc.)
  • Cancer or receiving radiotherapy and chemotherapy within 5 years
  • Severe pituitary or thyroid diseases
  • Suffering from AIDS, hepatitis A, hepatitis B and other infectious diseases
  • Mental disorders or current use of antidepressants

Sites / Locations

  • Sir Run Run Shaw Hospital;Hangzhou Dianzi University;China Jiliang University; Zhejiang Sci-Tech University

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

Routine education group

Programmed smartphone intervention group

Programmed smartphone plus dietitian intervention group

Arm Description

350-400 subjects aged 20-65 years with high metabolic risk

350-400 subjects aged 20-65 years with high metabolic risk

350-400 subjects aged 20-65 years with high metabolic risk

Outcomes

Primary Outcome Measures

Weight
Weight will be assessed by Seca-255 (ScalesGalore) during each visit ,weight will also be assessed by Wi-Fi scale at home
Height
Height will be assessed by Seca-255 (ScalesGalore) during each visit
Waist circumference
Waist circumference will be assessed by Seca-201(ScalesGalore) during each visit
Blood pressure
Both systolic pressure and diastolic pressure will be assessed using electronic blood pressure monitor (Omron J750)during each visit and at home
Triglyceride
Values at fasting and postprandial 60min and 3hours will be measured
Total cholesterol
Values at fasting and postprandial 60min and 3hours will be measured
LDL-C
Values at fasting and postprandial 60min and 3hours will be measured
HDL-C
Values at fasting and postprandial 60min and 3hours will be measured
Glucose
Values at fasting and postprandial 60min and 3hours will be measured

Secondary Outcome Measures

HbA1c
Values at fasting and postprandial 60min and 3hours will be measured
Insulin
Values at fasting and postprandial 60min and 3hours will be measured
Glucagon
Values at fasting and postprandial 60min and 3hours will be measured
Glucagon-like peptide-1
Values at fasting and postprandial 60min and 3hours will be measured
Gastric inhibitory peptide
Values at fasting and postprandial 60min and 3hours will be measured
Aspartate transaminase
Values at fasting and postprandial 60min and 3hours will be measured
Alanine aminotransferase
Values at fasting and postprandial 60min and 3hours will be measured
γ-glutamyl transpeptidase
Values at fasting and postprandial 60min and 3hours will be measured
Serum creatinine
Values at fasting and postprandial 60min and 3hours will be measured
Urine creatinine
Values at fasting and postprandial 60min and 3hours will be measured
Urea nitrogen
Values at fasting and postprandial 60min and 3hours will be measured
Uric acid
Values at fasting and postprandial 60min and 3hours will be measured

Full Information

First Posted
January 14, 2021
Last Updated
February 3, 2021
Sponsor
Chinese Academy of Sciences
Collaborators
Sir Run Run Shaw Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04714723
Brief Title
Lifestyle Intervention Trial in High Metabolic Risk Chinese
Official Title
Lifestyle Intervention Trial in High Metabolic Risk Chinese
Study Type
Interventional

2. Study Status

Record Verification Date
February 2021
Overall Recruitment Status
Not yet recruiting
Study Start Date
February 20, 2021 (Anticipated)
Primary Completion Date
September 30, 2021 (Anticipated)
Study Completion Date
December 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chinese Academy of Sciences
Collaborators
Sir Run Run Shaw Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
In this single-blind, randomized trial, about 1200 eligible volunteers, who have higher metabolic syndrome (MetS) risk and aged 20-65 years, will be assigned to one of three smartphone-based lifestyle intervention arms: 1) Routine education; 2) Programmed-smartphone intervention; and 3) Programmed-smartphone plus dietitian intervention. Before and after 6-month intervention, "PhenFlex test" (PFT) will be performed to examine and quantify improved metabolic flexibility. This intervention trial will be conducted by researchers in Shanghai Institute of Nutrition and Health of the Chinese Academy of Sciences (CAS) collaborating with Zhejiang University affiliated Sir Run Run Shaw Hospital. The study protocol was approved by the Ethics Committees in Shanghai Institutes of Nutrition and Health, and in Sir Run Run Shaw Hospital. The main aims of this study are to determine 1) efficacy of lifestyle interventions with different intensity in reducing MetS and its risk factors; 2) improved metabolic responses or flexibility defined by PFT-based homeostasis index; and 3) major genetic and nongenetic determinants for the efficacy of interventions among high MetS risk Chinese.
Detailed Description
Metabolic syndrome, a cluster of multiple metabolic disturbances, including central obesity, dyslipidemia, hypertension, and hyperglycemia, is associated with 2-5-fold heightened risks of CVD and T2D. Compelling evidence showed that lifestyle intervention is one of effective approaches for preventing and controlling cardiometabolic diseases. However, there were considerably variations among different interventions and different persons. With widely available smartphone and APP-connected wearable devises, it is possible to provide programmed nutrition and lifestyle education to help participants achieve intervention targets, and closely monitor compliance. However, few studies investigated the efficacy of lifestyle interventions with programmed smartphone and APP-connected wearable devises in MetS management. Moreover, since present disease-based diagnoses and biomarkers may not adequately define health status, the concept of "re-redefining health" has attracted growing attention. The phenotypic flexibility and "PhenFlex test" are one of approaches to measure individuals' adaptive capacity to maintain hemostatic condition after having a standardized challenge drinker. To date, the PFT has been studied among 10,000 subjects in western countries and few studies, if any, have conducted in Chinese who have different genetic background and dietary patterns. It remains to be established whether and to what extent that the PFT-based hemostatic index system can precisely evaluate the metabolic health in Chinese. In the current trial, approximate 1200 subjects with MetS risks will be randomly assigned to one of three smartphone-based lifestyle intervention arms: 1) Routine education; 2) Programmed-smartphone intervention; and 3) Programmed-smartphone plus dietitian intervention. The intervention duration will be 6-month and then have 2-year follow-up. During starting and end of 6-month intervention, we will include PFT during the physical examination hold in the Sir Run Run Shaw Hospital. All the subjects will be given a standardized challenge drinker (75g glucose, 60 fat and 20g protein). Fasting and multiple postprandial time points samples (blood, t=0,1,3h) and urine and feces will be collected to measure clinical and omics markers like metabolomics, gut microbiota and SNPs. Finally, the homeostasis index will be built to estimate improvement of individual metabolic health after the intervention. In conclusion, this study will provide scientific evidence and novel insights about the effectiveness of new intervention strategies and precise diagnostic and assessment system for cardiometabolic management.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Metabolic Syndrome X
Keywords
metabolic risk, lifestyle intervention, homeostasis

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
1200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Routine education group
Arm Type
Experimental
Arm Description
350-400 subjects aged 20-65 years with high metabolic risk
Arm Title
Programmed smartphone intervention group
Arm Type
Experimental
Arm Description
350-400 subjects aged 20-65 years with high metabolic risk
Arm Title
Programmed smartphone plus dietitian intervention group
Arm Type
Experimental
Arm Description
350-400 subjects aged 20-65 years with high metabolic risk
Intervention Type
Behavioral
Intervention Name(s)
Routine education
Intervention Description
Routine lifestyle education based on smartphone for six month
Intervention Type
Behavioral
Intervention Name(s)
Programmed smartphone intervention
Intervention Description
Interactive programmed lifestyle education based on smartphone for six month
Intervention Type
Behavioral
Intervention Name(s)
Programmed smartphone plus dietitian intervention
Intervention Description
Interactive programmed lifestyle education based on smartphone plus dietitians support for six month
Primary Outcome Measure Information:
Title
Weight
Description
Weight will be assessed by Seca-255 (ScalesGalore) during each visit ,weight will also be assessed by Wi-Fi scale at home
Time Frame
6 months
Title
Height
Description
Height will be assessed by Seca-255 (ScalesGalore) during each visit
Time Frame
6 months
Title
Waist circumference
Description
Waist circumference will be assessed by Seca-201(ScalesGalore) during each visit
Time Frame
6 months
Title
Blood pressure
Description
Both systolic pressure and diastolic pressure will be assessed using electronic blood pressure monitor (Omron J750)during each visit and at home
Time Frame
6 months
Title
Triglyceride
Description
Values at fasting and postprandial 60min and 3hours will be measured
Time Frame
6 months
Title
Total cholesterol
Description
Values at fasting and postprandial 60min and 3hours will be measured
Time Frame
6 months
Title
LDL-C
Description
Values at fasting and postprandial 60min and 3hours will be measured
Time Frame
6 months
Title
HDL-C
Description
Values at fasting and postprandial 60min and 3hours will be measured
Time Frame
6 months
Title
Glucose
Description
Values at fasting and postprandial 60min and 3hours will be measured
Time Frame
6 months
Secondary Outcome Measure Information:
Title
HbA1c
Description
Values at fasting and postprandial 60min and 3hours will be measured
Time Frame
6 months
Title
Insulin
Description
Values at fasting and postprandial 60min and 3hours will be measured
Time Frame
6 months
Title
Glucagon
Description
Values at fasting and postprandial 60min and 3hours will be measured
Time Frame
6 months
Title
Glucagon-like peptide-1
Description
Values at fasting and postprandial 60min and 3hours will be measured
Time Frame
6 months
Title
Gastric inhibitory peptide
Description
Values at fasting and postprandial 60min and 3hours will be measured
Time Frame
6 months
Title
Aspartate transaminase
Description
Values at fasting and postprandial 60min and 3hours will be measured
Time Frame
6 months
Title
Alanine aminotransferase
Description
Values at fasting and postprandial 60min and 3hours will be measured
Time Frame
6 months
Title
γ-glutamyl transpeptidase
Description
Values at fasting and postprandial 60min and 3hours will be measured
Time Frame
6 months
Title
Serum creatinine
Description
Values at fasting and postprandial 60min and 3hours will be measured
Time Frame
6 months
Title
Urine creatinine
Description
Values at fasting and postprandial 60min and 3hours will be measured
Time Frame
6 months
Title
Urea nitrogen
Description
Values at fasting and postprandial 60min and 3hours will be measured
Time Frame
6 months
Title
Uric acid
Description
Values at fasting and postprandial 60min and 3hours will be measured
Time Frame
6 months
Other Pre-specified Outcome Measures:
Title
E-selectin concentration
Description
Concentration at fasting and postprandial 60min and 3hours will be measured
Time Frame
6 months
Title
P-selectin concentration
Description
Concentration at fasting and postprandial 60min and 3hours will be measured
Time Frame
6 months
Title
Vascular cell adhesion molecule-1(VCAM-1) concentration
Description
Concentration at fasting and postprandial 60min and 3hours will be measured
Time Frame
6 months
Title
Intercellular adhesion molecule-1 (ICAM-1) concentration
Description
Concentration at fasting and postprandial 60min and 3hours will be measured
Time Frame
6 months
Title
Amyloid A1(SAA1) concentration
Description
Concentration at fasting and postprandial 60min and 3hours will be measured
Time Frame
6 months
Title
Tumor Necrosis Factor-α (TNF-α) concentration
Description
Concentration at fasting and postprandial 60min and 3hours will be measured
Time Frame
6 months
Title
Interleukin-10(IL-10) concentration
Description
Concentration at fasting and postprandial 60min and 3hours will be measured
Time Frame
6 months
Title
Interleukin-1b(IL-1b) concentration
Description
Concentration at fasting and postprandial 60min and 3hours will be measured
Time Frame
6 months
Title
C-reactive protein(CRP) concentration
Description
Concentration at fasting and postprandial 60min and 3hours will be measured
Time Frame
6 months
Title
Retinol binding protein(RBP4) concentration
Description
Concentration at fasting and postprandial 60min and 3hours will be measured
Time Frame
6 months
Title
Adiponectin concentration
Description
Concentration at fasting and postprandial 60min and 3hours will be measured
Time Frame
6 months
Title
Metabolomics including profiling of free fatty acids and other metabolites
Description
Metabolomics will be measured by LC-MS
Time Frame
6 months
Title
Single nucleotide polymorphism (SNPs)
Description
Mutations at specific sites will be detected by gene chip
Time Frame
baseline
Title
Gut microbiota 16S rDNA sequencing
Description
Gut microbiota 16S rDNA will be sequenced
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Volunteers at high metabolic risk aged 20-65 who didn't participate in other studies in 3 months before the current research, having a certain level of education and normal cognitive ability, taking good care of himself/herself at least meet three of the following criterions(NCEP- ATPIII, for Asian Americans): Waist circumference ≥90 cm (men), ≥ 80 cm (women). total triglyceride ≥ 1.7 mmol/L. HDL-c <1.03 mmol/L in men, <1.3 mmol/L in women. systolic blood pressure ≥ 130 mmHg or diastolic blood pressure ≥ 85mmHg. Fasting plasma glucose ≥ 5.6 mmol/L. Exclusion Criteria: Fasting glucose>7.0mmol/L or diagnosed diabetes or taking insulin or other blood glucose-lowering drugs Diagnosed phase three hypertension or can't lowering SBP under 160mmHg after anti-hypertension drugs Fasting blood TG≥ 5.7 mmol/L or fasting LDL-C≥ 4.9 mmol/L or taking lipid-lowering drugs Pregnancy or lactation Obvious drug changing in three months before research History of drug or alcohol abuse or other substance abuse (Alcohol abuse is defined as more than 40 g/day of alcohol for woman, and more than 80g/day for man) Severe kidney and liver diseases (blood biomarkers such as alt, serum creatinine is 1.5 times over the scope of normal setting) Severe Gastrointestinal diseases (such as severe diarrhea, constipation, severe digestive tract inflammation, active peptic ulcer, acute cholecystitis, etc.) Having surgeries within one year before research such as heart stents implanted surgery (expect for appendicitis or hernia operation) Severe cardiovascular disease (e.g., heart failure, myocardial infarction, cerebral infarction, and acute myocarditis, severe arrhythmia, received the intervention therapy, etc.) Cancer or receiving radiotherapy and chemotherapy within 5 years Severe pituitary or thyroid diseases Suffering from AIDS, hepatitis A, hepatitis B and other infectious diseases Mental disorders or current use of antidepressants
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Xiaowei Yang, PhDcandidate
Phone
86-21-54920910
Email
yangxiaowei2018@sibs.ac.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Xu Lin, PhD
Organizational Affiliation
Shanghai Institute of Nutrition and Health, Chinese Acadamy of Sciences
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sir Run Run Shaw Hospital;Hangzhou Dianzi University;China Jiliang University; Zhejiang Sci-Tech University
City
Hangzhou
State/Province
Zhejiang
ZIP/Postal Code
310016
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xiaowei Yang, PhDcandidate
Phone
86-21-54920712
Email
yangxiaowei2018@sibs.ac.cn
First Name & Middle Initial & Last Name & Degree
Lihong Wu, MD
Email
wulihongxx@163.com
First Name & Middle Initial & Last Name & Degree
Xu Lin, PhD
First Name & Middle Initial & Last Name & Degree
Liying Chen, PhD

12. IPD Sharing Statement

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Lifestyle Intervention Trial in High Metabolic Risk Chinese

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