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NCT Number: NCT05439226

Liver Fat as a Dietary Target of the Chinese Medical Nutrition Therapy (CMNT) Diet for Treating Type 2 Diabetes With Nonalcoholic Fatty Liver Disease

Type 2 diabetes (T2D) represents a serious public health problem. Patients with T2D and non-alcoholic fatty liver disease(NAFLD) demonstrate a poor metabolic profile and increase mortality compared with patients with only NAFLD or T2D. Nutritional intervention is the most basic treatment for T2D. Previous study showed that a Chinese medical nutrition therapy (CMNT) diet, which intermittent use of low-calorie medicinal food, has a glucose-lowering effect in T2D. This study aims to investigate the effect of a Chinese medical nutrition therapy (CMNT) diet accompanied by intermittent energy restriction on reducing liver fat and glycated hemoglobin (HbA1c) in patients with T2D and NAFLD.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Physical Examination Center of Gezhouba central hospital of Sinopharm, Yichang, Hubei, China

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About this study

Diet composition of CMNT is a multicomponent Chinese medicinal food, which mainly enriched with whole grains and edible medicine and food homologous (MFH) plants such as Rhizoma Dioscoreae, Momordica Grosvenori, Folium Mori, Radix Puerariae, Fructus lycii, Poria cocos that meets the requirements of a food for special medical purpose. The CMNT group was instructed to consumed the provided CMNT diet consisting of 6 cycles of 5 consecutive days followed by 10 days of ad libitum food consumption. Participants received a 917 kcal/day preprepared human CMNT diet (44.75% carbohydrate, 9.1% protein and 46.15% fat) for 5 consecutive days per cycle. CMNT diet is composed of four ready-to-consume prepared foods including composite nutritional rice, solids beverages, meal replacement biscuit and fruit and vegetable gruel mainly from wholegrains and traditional Chinese medicinal food plants. The intervention lasted for 3 months (6 cycles) and follow-up measurements will be performed in all subjects after 3-months from end of the intervention. The glucose-lowering medication use of participants strictly implemented by their physician according to the diabetes medications management protocol. Treatment-as-usual control group continued to be given standard medication and dietary advice by their physician followed guidelines for the prevention and control of T2D in China.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients diagnosed with type 2 diabetes and NAFLD
  • Age between 18 and 75 years
  • BMI between 18.0 and 35.0 kg/m2
  • Weight stable for at least 3 months prior to the study (gain or loss < 4 kg)
  • Stable treatment for at least 3 months with 1-3 oral antidiabetic medications (with or without insulin therapy), or not yet received antidiabetic medication prior to the beginning of the study
  • Able to give written informed consent

Exclusion criteria

  • Self-reported a food allergy
  • Alcohol abuse in the last 3 months (alcohol intake greater than 20 g per day for women; Alcohol intake for men greater than 40 g per day)
  • Other liver diseases such as chronic hepatitis B and C, autoimmune hepatitis, primary biliary cirrhosis, hemochromatosis, nodular regenerative hyperplasia and focal nodular hyperplasia
  • Scheduled to be hospitalized for any surgical treatment during screening
  • Pregnant or planning of pregnancy during the study
  • Inability, physically or mentally, to adhere the procedures required by the study protocol
  • Level 3 hypoglycemic events (at least 3 times) occurring within the 90 days prior to screening
  • Hospitalization or emergency department visit for hyperglycemia, diabetic ketoacidosis, lactic acidosis, hyperosmolar nonketotic coma, or diabetes
  • History of cancer within the past 5 years
  • Acute coronary or cerebrovascular event in the past 90 days, or heart failure
  • Hemorrhagic or ischemic stroke within the last 6 months

Treatment and study plan

CMNT diet

Other

Hypocaloric CMNT diet plan: A diet plan with intermittent use of enriched traditional-Chinese-medicinal-foods CMNT diet

Primary outcomes

  1. Controlled attenuation parameter (CAP) value by transient elastography

    Time frame: 3, 6, 12, 24 months

    The CAP score, which be measured by FibroScan, will be used to quantify and detect liver fat. CAP < 238 dB/m indicated no hepatic steatosis, 238 ≤ CAP ≤ 259 dB/m denoted mild steatosis, 260 ≤ CAP ≤291 dB/m indicated moderate steatosis, and CAP > 291 dB/m denoted severe steatosis.

  2. HbA1C

    Time frame: 3, 6, 12, 24 months

    Blood test to measure glucose control

Secondary outcomes

  1. Fatty liver index (FLI)

    Time frame: 3, 6, 12, 24 months

    FLI will also be applied to quantify the degree of steatosis of patients with type 2 diabetes and NAFLD. FLI values < 30 rule out liver steatosis, whereas FLI ≥ 60 confirmed NAFLD with a specificity of 61%.

  2. Hepatic steatosis index (HSI)

    Time frame: 3, 6, 12, 24 months

    HSI will also be applied to quantify the degree of steatosis of patients with type 2 diabetes and NAFLD. HSI values < 30 excludes NAFLD with a sensitivity of 93.1%, while values > 36 detected NAFLD with a specificity of 92.4%.

  3. Liver stiffness measurement (LSM) value by transient elastography

    Time frame: 3, 6, 12, 24 months

    Liver fibrosis will be assessed by using a non-invasive vibration-controlled transient elastography to estimate LSM. A median LSM ≥ 8.2 kPa was considered indicative of significant fibrosis (≥ F2), whereas LSM ≥ 9.7 kPa was considered indicative of advanced (≥ F3) fibrosis, whereas LSM ≥ 13.6 kPa was considered indicative of cirrhosis (F4).

  4. Fibrosis-4 index (FIB-4)

    Time frame: 3, 6, 12, 24 months

    The FIB-4 index, a non-invasive measurement, will be used to evaluate the degree of liver fibrosis. The FIB-4 index <1.45 had a negative predictive value of 94.7% to exclude progressive fibrosis, whereas FIB-4 index >3.25 was considered advanced fibrosis or cirrhosis.

  5. NAFLD fibrosis score (NFS)

    Time frame: 3, 6, 12, 24 months

    Degree of liver fibrosis will also be assessed by NFS.The probability of advanced liver fibrosis was classified into three groups: high NFS (NFS > 0.676), intermediate NFS (NFS: -1.455 to 0.676, or 0.120 to 0.676 if age > 65), or low NFS (NFS < -1.455, or < 0.120 if age > 65) .

  6. Liver function test

    Time frame: 3, 6, 12, 24 months

    γ-glutamyl transferase (γ-GGT), alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP) and ect will be assessed.

  7. Blood glucose

    Time frame: 3, 6, 12, 24 months

    Fasting plasma glucose (FPG) and postprandial 2-hour plasma glucose (2 h-PG)

  8. Blood lipid

    Time frame: 3, 6, 12, 24 months

    triglyceride, total cholesterol, low-density lipoprotein cholesterol (LDL-C) and high-density lipoprotein-cholesterol (HDL-C)

  9. Insulin

    Time frame: 3, 6, 12, 24 months

    Glucose homeostasis

  10. HOMA-IR

    Time frame: 3, 6, 12, 24 months

    Fasting glucose times fasting insulin divided by 22.5

  11. IGF-1

    Time frame: 3, 6, 12, 24 months

    Glucose homeostasis

  12. Body mass index

    Time frame: 3, 6, 12, 24 months

    Body mass in kilograms divided by height in meters squared.

  13. waist-to-hip ratio

    Time frame: 3, 6, 12, 24 months

    Waist circumference in centimeter divided by height in centimeter.

  14. Blood pressure

    Time frame: 3, 6, 12, 24 months

    Systolic blood pressure and diastolic blood pressure.

  15. Energy intake

    Time frame: 3, 6, 12, 24 months

    3-day diet record and Food Frequency Questionnaire

  16. Macronutrient intake

    Time frame: 3, 6, 12, 24 months

    3-day diet record and Food Frequency Questionnaire

  17. Sleep quality

    Time frame: 3, 6, 12, 24 months

    Pittsburgh Sleep Quality Index Questionnaire

  18. Physical activity

    Time frame: 3, 6, 12, 24 months

    International Physical Activity Questionnaire

  19. Self-reported depressive symptoms

    Time frame: 3, 6, 12, 24 months

    Patient Health Questionnaire 9

  20. Anxiety symptoms

    Time frame: 3, 6, 12, 24 months

    Generalized Anxiety Disorder scale

  21. Social support

    Time frame: 3, 6, 12, 24 months

    Social Support Rate Scale

  22. Reduction in glucose-lowering medication

    Time frame: 3, 6, 12, 24 months

    Reduction in total dose of glucose-lowering medications

  23. Fecal microbiota profile

    Time frame: 3, 6, 12, 24 months

    Fecal samples will be collected and will be sequenced.

  24. Metabolomics

    Time frame: 3, 6, 12, 24 months

    Blood, fecal and urine samples will be collected and metabolites will be analyzed through a metabolomics approach.

Study contacts

Contact information is provided by the study sponsor or research team.

Sponsors and collaborators

Lead sponsor

State Key Laboratory of Subhealth Intervention Technology

Other

Registry information

Important dates

Study start
2022
Primary completion
2026
Study completion
2026
First posted
Jun 30, 2022
Registry last updated
Jul 25, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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