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

Sponsor
Westlake University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05885828
Collaborator
Hangzhou Third People's Hospital (Other)
1,500
1
2
126.1
11.9

Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Other: White bread
  • Other: Whole wheat bread
  • Behavioral: Plant-based diet
  • Other: Conventional diabetic diet
  • Other: Follow-up visit every 1-2 years
N/A

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
1500 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Investigator, Outcomes Assessor)
Primary Purpose:
Other
Official Title:
The PRECISION-T2D Study: Precision Nutrition Study for Type 2 Diabetes
Anticipated Study Start Date :
May 30, 2023
Anticipated Primary Completion Date :
Dec 1, 2024
Anticipated Study Completion Date :
Dec 1, 2033

Arms and Interventions

Arm Intervention/Treatment
Experimental: Plant-based diet

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.

Other: White bread
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.
Other Names:
  • Breakfast A
  • Other: Whole wheat bread
    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.
    Other Names:
  • Breakfast B
  • Behavioral: Plant-based diet
    After wearing CGM on Day 1, participants will be asked to follow the plant-based diet in next 30 days.

    Other: Follow-up visit every 1-2 years
    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.

    Experimental: Conventional diabetic diet

    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.

    Other: White bread
    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.
    Other Names:
  • Breakfast A
  • Other: Whole wheat bread
    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.
    Other Names:
  • Breakfast B
  • Other: Conventional diabetic diet
    Volunteers will be asked to have a diet following 2023 Chinese Diabetes Society guidelines in next 30 days.

    Other: Follow-up visit every 1-2 years
    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.

    Outcome Measures

    Primary Outcome Measures

    1. Changes in gut microbiome profile [Day 1 and Day 31]

      Shotgun metagenomic sequencing will be performed in stool samples.

    2. Blood glucose profile [2 weeks]

      Real-time blood glucose fluctuations will be recorded using continuous glucose monitoring.

    Secondary Outcome Measures

    1. Carotid plaque [At enrollment]

      Grade carotid plaque using ultrasound.

    2. Carotid intima-media thickness [At enrollment]

      Measure of carotid intima-media thickness using ultrasound.

    3. Number of participants with chronic kidney disease [Up to 10 years]

      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.

    4. Cognitive function [Up to 10 years]

      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.

    5. Changes in fasting blood glucose [Day 1 and Day 31]

      Fasting glucose will be examined in mmol/L.

    6. Changes in fasting blood C-peptide [Day 1 and Day 31]

      Fasting blood C-peptide will be examined in μg/L.

    7. Changes in fasting blood HbA1c [Day 1 and Day 31]

      Fasting blood HbA1c will be examined in %.

    8. Changes in lipid metabolism [Day 1 and Day 31]

      Triglyceride, cholesterol, high density lipoprotein cholesterol and low density lipoprotein cholesterol will be examined in mmol/L.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    35 Years to 70 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    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

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Hangzhou Third People's Hospital Hangzhou Zhejiang China 310058

    Sponsors and Collaborators

    • Westlake University
    • Hangzhou Third People's Hospital

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Westlake University
    ClinicalTrials.gov Identifier:
    NCT05885828
    Other Study ID Numbers:
    • 20230306ZJS002
    First Posted:
    Jun 2, 2023
    Last Update Posted:
    Jun 2, 2023
    Last Verified:
    Mar 1, 2023
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Westlake University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jun 2, 2023