Skip to content

Personalized Nutrition Services to Reduce Postprandial Glucose Levels Using Gut Microbiota and Artificial Intelligence

Personalized Nutrition Services to Reduce Postprandial Glucose Levels Using Gut Microbiota and Artificial Intelligence

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20251016021
Enrollment
200
Registered
2025-10-16
Start date
2025-11-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Postprandial Hyperglycemia Prediabetes Type 2 Diabetes Mellitus precision nutrition postprandial glucose gut microbiota artificial intelligence Thai food

Interventions

The intervention is an 14-day personalized nutrition program. Upon enrollment, all 200 participants will undergo a baseline assessment that includes a review of their medical and dietary history, phys
Experimental Other

Sponsors

Program Management Unit for Competitiveness (PMUC)
Lead Sponsor
Modish Food Design Co., Ltd.
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Age 18-80 years. 2. Body Mass Index (BMI) greater than 18.5 kg/m2. 3. Participants may have normal blood glucose, prediabetes (fasting plasma glucose 100-125 mg/dL or HbA1c 5.7-6.5 percent), or type 2 diabetes treated with lifestyle modification, metformin, and or pioglitazone with an HbA1c level less than or equal to 9 percent. 4. If on medication for hypertension, diabetes (metformin), or hyperlipidemia, the dosage must be stable for at least 3 months prior to enrollment. 5. Must own a smartphone capable of installing the necessary application for the continuous glucose monitoring (CGM) system.

Exclusion criteria

Exclusion criteria: 1.History of allergy to food or components in the study products. 2.Significant weight change (greater than 5 kg) within 6 weeks before the study. 3.Severe uncontrolled hypertension (greater than or equal to 180 over 110 mmHg) or hypertriglyceridemia (greater than 500 mg per dL). 4.HbA1c greater than 9 percent or fasting plasma glucose greater than 200 mg per dL. 5.Use of steroids or antibiotics within 6 weeks before the study. 6.Pregnant or lactating. History of diseases affecting digestion and absorption (e.g., short bowel syndrome, inflammatory bowel disease, chronic pancreatitis). 7.Previous bariatric surgery.

Design outcomes

Primary

MeasureTime frame
Change in Postprandial Glycemic Response. over 14-day period of dietary intervention Glucose levels measured via a continuous glucose monitoring (CGM) device every 5 minutes for 14 days. Analysis will include standard metrics such as Area Under the Curve (AUC).

Secondary

MeasureTime frame
Gut microbiota composition Baseline Analysis of stool samples using 16S rRNA sequencing to determine the relative abundance of microbial genera.,Metabolic markers Baseline Blood tests including fasting plasma glucose, fasting insulin, HbA1c, and lipid profile (total cholesterol, triglycerides, HDL and LDL cholesterol).

Countries

Thailand

Contacts

Public ContactPornpoj Pramyothin

Mahidol University

pornpoj.pra@mahidol.edu0895140091

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026