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The PRECISION-T2D Study: Precision Nutrition Study for Type 2 Diabetes

Primary Purpose

Type 2 Diabetes

Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
White bread
Whole wheat bread
Plant-based diet
Conventional diabetic diet
Follow-up visit every 1-2 years
Sponsored by
Westlake University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Type 2 Diabetes focused on measuring N-of-1, plant-based diet, precision nutrition, continuous glucose monitoring, type 2 diabetes

Eligibility Criteria

35 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Diagnosed with type 2 diabetes; Living in Hangzhou for at least five years; Have the willingness or ability to complete the intervention and sample collection Exclusion Criteria: Mental and physical disability; Already is a vegetarian; Cancer and serious complications from type 2 diabetes, such as renal failure; Using insulin for more than 5 years; Unstable medical/medication status; Current alcohol or drug abuse; Taking antibiotics in the last three months

Sites / Locations

  • Westlake UniversityRecruiting
  • Hangzhou Third People's HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Plant-based diet

Conventional diabetic diet

Arm Description

Participants in this arm will be recommended to consume more fiber-rich foods, including whole grains, fruits, legumes and vegetables; to moderate their intake of fish, eggs and dairy products; and to avoid other animal products. All participants are instructed not to modify their exercise habits during the intervention period. Additionally, if a participant is hospitalized during the intervention, a standardized plant-based diet will be provided.

Participants in this arm will be recommended to have a diet following 2023 Chinese Diabetes Society guidelines. All participants are instructed not to modify their exercise habits during the intervention period. If a participant is hospitalized during the intervention, a standardized diabetic diet will be provided.

Outcomes

Primary Outcome Measures

Changes in gut microbiome profile
Shotgun metagenomic sequencing will be performed in stool samples.
Blood glucose profile
Real-time blood glucose fluctuations will be recorded using continuous glucose monitoring.

Secondary Outcome Measures

Carotid plaque
Grade carotid plaque using ultrasound.
Carotid intima-media thickness
Measure of carotid intima-media thickness using ultrasound.
Number of participants with chronic kidney disease
The serum creatine and urine creatine and protein will be measured and chronic kidney disease will be defined as an estimated glomerular filtration rate of <60 mL/min/1.73 m2 or and the presence of an elevated urine microalbumin/creatinine ratio. All cases will be verified by medical record review.
Cognitive function
Cognitive function was measured by the Addenbrooke's Cognitive Examination-Revised (ACE-R). The original 26 components were combined to produce five subscores, 100 in total. The cutoff for dementia is 82-88/100.
Changes in fasting blood glucose
Fasting glucose will be examined in mmol/L.
Changes in fasting blood C-peptide
Fasting blood C-peptide will be examined in μg/L.
Changes in fasting blood HbA1c
Fasting blood HbA1c will be examined in %.
Changes in lipid metabolism
Triglyceride, cholesterol, high density lipoprotein cholesterol and low density lipoprotein cholesterol will be examined in mmol/L.

Full Information

First Posted
March 23, 2023
Last Updated
August 1, 2023
Sponsor
Westlake University
Collaborators
Hangzhou Third People's Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05885828
Brief Title
The PRECISION-T2D Study: Precision Nutrition Study for Type 2 Diabetes
Official Title
The PRECISION-T2D Study: Precision Nutrition Study for Type 2 Diabetes
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
July 17, 2023 (Actual)
Primary Completion Date
December 1, 2024 (Anticipated)
Study Completion Date
December 1, 2033 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Westlake University
Collaborators
Hangzhou Third People's 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
Food plays a crucial role in determining blood glucose levels, especially in people with type 2 diabetes. Precision nutrition, which involves individually tailored dietary interventions, can be a powerful tool in managing blood glucose levels in people with type 2 diabetes. Previous studies found that changes in gut microbiota resulted from the dietary intervention, such as plant-based diet, might subsequently lead to different glycemic responses, and then different health outcomes. In this study, the investigators will characterize the blood glucose dynamics and gut microbiota of individuals with type 2 diabetes. They aim to assess the influence of plant-based diet on gut microbiota; they will also investigate the influence of gut microbiota on glycemic responses. Additionally, a series of individual N-of-1 trails will be integrated to compare the effects of a white bread breakfast and a whole wheat bread breakfast on glucose metabolism at the individual level.
Detailed Description
Choice of design: The study is a two-arm intervention study integrated with N-of-1 design. Study population: Patients with type 2 diabetes. Screening Assessment: Prospective participants will be selected based on the pre-defined inclusion and exclusion criteria. Recruitment will be done over the phone and via the social media. Study duration: Each participant will take part in the study for a period of up to 1 month at baseline and have follow-up visits every 1-2 years. Dietary intervention: The PRECISION-T2D study will be divided into two subcohorts at baseline. Cohort 1 (n=1,200) will complete a home-based dietary intervention, while Cohort 2 (n=300) will complete a ward-based dietary intervention. In each cohort, participants will be randomly assigned to two groups: plant-based diet and conventional diabetic diet. Participants in the plant-based diet arm will be recommended to consume more fiber-rich foods, including whole grains, fruits, legumes and vegetables; to moderate their intake of fish, eggs and dairy products; and to avoid other animal products. Participants in the conventional diabetic diet arm will be recommended to have a diet following 2023 Chinese Diabetes Society guidelines. During the baseline visit (day one to day twelve), all participants (n=1,500) will be given standardized meals for breakfast. Participants who continue onto the home-based intervention will receive dietary recommendations on lunch and dinner meals, lasting up to one month following their clinical visit. Each participant will be provided with a list of recommended foods. Participants who continue onto the ward-based intervention will be given standardized meals for lunch and dinner. Participants will be asked to consume the entire amount of food indicated for the standardized meals and to record any leftover food. All participants will be asked to track their meals, snacks and drinks with instructions on how to record their daily dietary information. Participants will also be advised not to modify their exercise habits during the course of the study. During the participants' first baseline visit day, they will be asked to complete a baseline questionnaire to collect information on their lifestyle, dietary habits, history of medications, sleep quality and appetite. Anthropometric measurements, ultrasonography evaluation, and laboratory tests will be taken using standard protocols. Participants will then be asked to wear a continuous glucose monitor (CGM) for 14-day blood glucose monitoring, which will be done by a nurse. On day 14, participants will be asked to come in for a clinical visit where they will receive their CGM report and provide blood, saliva, urine and stool samples. On day 30, participants will be asked to come in for another clinical visit where they will undergo a liver MRI (Magnetic Resonance Imaging) scan and provide blood, saliva, urine and stool samples.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 2 Diabetes
Keywords
N-of-1, plant-based diet, precision nutrition, continuous glucose monitoring, type 2 diabetes

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
1500 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Plant-based diet
Arm Type
Experimental
Arm Description
Participants in this arm will be recommended to consume more fiber-rich foods, including whole grains, fruits, legumes and vegetables; to moderate their intake of fish, eggs and dairy products; and to avoid other animal products. All participants are instructed not to modify their exercise habits during the intervention period. Additionally, if a participant is hospitalized during the intervention, a standardized plant-based diet will be provided.
Arm Title
Conventional diabetic diet
Arm Type
Experimental
Arm Description
Participants in this arm will be recommended to have a diet following 2023 Chinese Diabetes Society guidelines. All participants are instructed not to modify their exercise habits during the intervention period. If a participant is hospitalized during the intervention, a standardized diabetic diet will be provided.
Intervention Type
Other
Intervention Name(s)
White bread
Other Intervention Name(s)
Breakfast A
Intervention Description
After wearing CGM on Day 1, participants will be provided with white bread (76-77g) and milk (250mL) for breakfast on Day 3, Day 4, Day 7, Day 8, Day 10, Day 12.
Intervention Type
Other
Intervention Name(s)
Whole wheat bread
Other Intervention Name(s)
Breakfast B
Intervention Description
After wearing CGM on Day 1, participants will be provided with wheat bread (85-86g) and milk (250mL) for breakfast on Day 2, Day 5, Day 6, Day 9, Day 11, Day 13.
Intervention Type
Behavioral
Intervention Name(s)
Plant-based diet
Intervention Description
After wearing CGM on Day 1, participants will be asked to follow the plant-based diet in next 30 days.
Intervention Type
Other
Intervention Name(s)
Conventional diabetic diet
Intervention Description
Volunteers will be asked to have a diet following 2023 Chinese Diabetes Society guidelines in next 30 days.
Intervention Type
Other
Intervention Name(s)
Follow-up visit every 1-2 years
Intervention Description
Participants will be visited every 1-2 years. At each visit, face-to-face interviews, specimen collection, anthropometric measurements, ultrasonography evaluation, laboratory tests, and multi-omics data will be conducted.
Primary Outcome Measure Information:
Title
Changes in gut microbiome profile
Description
Shotgun metagenomic sequencing will be performed in stool samples.
Time Frame
Day 1 and Day 31
Title
Blood glucose profile
Description
Real-time blood glucose fluctuations will be recorded using continuous glucose monitoring.
Time Frame
2 weeks
Secondary Outcome Measure Information:
Title
Carotid plaque
Description
Grade carotid plaque using ultrasound.
Time Frame
At enrollment
Title
Carotid intima-media thickness
Description
Measure of carotid intima-media thickness using ultrasound.
Time Frame
At enrollment
Title
Number of participants with chronic kidney disease
Description
The serum creatine and urine creatine and protein will be measured and chronic kidney disease will be defined as an estimated glomerular filtration rate of <60 mL/min/1.73 m2 or and the presence of an elevated urine microalbumin/creatinine ratio. All cases will be verified by medical record review.
Time Frame
Up to 10 years
Title
Cognitive function
Description
Cognitive function was measured by the Addenbrooke's Cognitive Examination-Revised (ACE-R). The original 26 components were combined to produce five subscores, 100 in total. The cutoff for dementia is 82-88/100.
Time Frame
Up to 10 years
Title
Changes in fasting blood glucose
Description
Fasting glucose will be examined in mmol/L.
Time Frame
Day 1 and Day 31
Title
Changes in fasting blood C-peptide
Description
Fasting blood C-peptide will be examined in μg/L.
Time Frame
Day 1 and Day 31
Title
Changes in fasting blood HbA1c
Description
Fasting blood HbA1c will be examined in %.
Time Frame
Day 1 and Day 31
Title
Changes in lipid metabolism
Description
Triglyceride, cholesterol, high density lipoprotein cholesterol and low density lipoprotein cholesterol will be examined in mmol/L.
Time Frame
Day 1 and Day 31

10. Eligibility

Sex
All
Minimum Age & Unit of Time
35 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosed with type 2 diabetes; Living in Hangzhou for at least five years; Have the willingness or ability to complete the intervention and sample collection Exclusion Criteria: Mental and physical disability; Already is a vegetarian; Cancer and serious complications from type 2 diabetes, such as renal failure; Using insulin for more than 5 years; Unstable medical/medication status; Current alcohol or drug abuse; Taking antibiotics in the last three months
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ju-Sheng Zheng, PhD
Phone
86-0571-88112056
Email
zhengjusheng@westlake.edu.cn
Facility Information:
Facility Name
Westlake University
City
Hangzhou
State/Province
Zhejiang
ZIP/Postal Code
310030
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Zelei Miao, PhD
Phone
86-0571-88112056
Email
miaozelei@westlake.edu.cn
First Name & Middle Initial & Last Name & Degree
Hang He, Master
Phone
86-0571-88112056
Email
hehang@westlake.edu.cn
First Name & Middle Initial & Last Name & Degree
Ju-Sheng Zheng, PhD
Facility Name
Hangzhou Third People's Hospital
City
Hangzhou
State/Province
Zhejiang
ZIP/Postal Code
310058
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Peng Li, Master
First Name & Middle Initial & Last Name & Degree
Yu Chen, Master
First Name & Middle Initial & Last Name & Degree
Peng Li, Master

12. IPD Sharing Statement

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The PRECISION-T2D Study: Precision Nutrition Study for Type 2 Diabetes

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