Lifestyle Modification for MAFLD Based on TTM

Lifestyle Modification for the Treatment of Metabolic Associated Fatty Liver Disease Based on Transtheoretical Model: a Single-center, Randomized, Controlled Study

Lifestyle changes aiming at weight loss remain the cornerstone of MAFLD treatment.Evaluating the motivational stage of patients' change and providing targeted lifestyle guidance may significantly improve the efficiency of weight loss. The investigators hypothesize that gut microbiota may affect motivation to lose weight, and the changes in gut microbiota due to weight loss may positively feedback the behavior of motivation, forming a virtuous circle. Thus, this study aims at ①evaluating the relationships between motivational stage of weight loss and the gut microbiota (Gut-brain axis); ②investigating the effects of lifestyle interventions on the gut microbiota in MAFLD patients.

Study Overview

Detailed Description

Fatty liver associated with metabolic dysfunction is common, affects a quarter of the population, and has no approved drug therapy. In 2020, two position articles have proposed not only the change of the terminology from NAFLD to metabolic associated fatty liver disease (MAFLD), but also an update and revision of the definition of fatty liver disease. According to these papers, indeed, the diagnosis of MAFLD can be made with the presence of hepatic steatosis (detected by serum biomarker scores, imaging methods or histology) and at least one of the fol- lowing metabolic criteria: (a) overweight/obesity, (b) T2DM and (c) metabolic dysregulation (that means at least two factors among increased waist circumference, hypertension, hypertriglyceridemia, low serum HDL-cholesterol levels, impaired fasting glucose, homeostatic model assessment of insulin resistance [HOMA-IR] > 2.5 or high sensitivity C-reactive protein > 2 mg/L). Here,the investigators focus on the obese NAFLD, which considered as a sub-phenotype in MAFLD.

Lifestyle changes aiming at weight loss remain the cornerstone of MAFLD treatment. However, it is not easy to make patients change their unhealthy lifestyle. Behavior therapy may only be successful in motivated patients, and motivation to dieting and exercising may be different according to age and sex. Personal motivation for change plays a pivotal role in behavior changes. The transtheoretical model (TTM) is an empirically validated model of individual behavioral change, which involves progress through a series of stages to make a particular behavioral change. TTM-based interventions have been applied to facilitate health behavioral changes, such as physical exercise, smoking cessation, and weight management, studies of which continue to demonstrate positive effects. Evaluating the motivational stage of patients' change and providing targeted lifestyle guidance may significantly improve the efficiency of weight loss. The investigators hypothesize that gut microbiota may affect motivation to lose weight, and the changes in gut microbiota due to weight loss may positively feedback the behavior of motivation, forming a virtuous circle.

Thus, a total of seventy obese patients with NAFLD will be recruited in this study, divided into lifestyle modification program group(n=35) and usual care group(n=35). All subjects will undergo dietary assessment based on Food Frequency Questionnaire ( FFQ) and motivational stages evaluation based on TTM. Stool samples will be collected at each visit. Demographic data will be recorded, consisted of age, weight, height, waist circumference, BMI, and so on. MRI-PDFF will be performed to evaluate liver steatosis. Meanwhile, vibration-controlled transient elastography will be carried out, which include liver stiffness (LSM) and controlled attenuation parameter (CAP) measurements. Biochemistry tests will be conducted as supplementary for assessment of NAFLD and cardiovascular risks, comprising liver function test, lipid, fasting glucose, etc.

The investigators aim at ①evaluating the relationships between motivational stage of weight loss and the gut microbiota (Gut-brain axis); ②investigating the effects of lifestyle interventions on the gut microbiota in MAFLD patients.

Study Type

Interventional

Enrollment (Anticipated)

75

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Guangdong
      • Guangzhou, Guangdong, China
        • Recruiting
        • Hepatology Unit, Department of Infectious Diseases, Nanfang Hospital, Southern Medical University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 80 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. With age range of 18-65 years.
  2. BMI ≥ 28kg/m2
  3. Fatty infiltration of the liver was confirmed on imaging studies (ultrasound, transient elastography, computed tomography, or magnetic resonance imaging) or liver biopsy.
  4. With valid motivational stage assessment based on TTM.
  5. Written consent form obtained.

Exclusion Criteria:

  1. History of other chronic liver disease (Viral hepatitis B or C, autoimmune hepatitis, cholestatic and Inherited metabolic liver diseases) and hemochromatosis.
  2. Self-reported HIV-positive status, active tuberculosis, active malaria, or inflammatory bowel disease.
  3. Excessive alcohol consumption (>30g/d for men and >20g/d for women).
  4. Patient has known cirrhosis (compensated/decompensated) either based on clinical criteria or liver histology or Imaging techniques.
  5. Subjects using thyroid hormones, oestrogens, amiodarone, steroids, tamoxifen and other medicine known to affect liver fat accumulation.
  6. Subjects using thiazolidinedione hypoglycemic drugs, vitamin E and other medicine have potential benefits for NASH within six months.
  7. Subjects with organ failure.
  8. Subjects with hepatocellular carcinoma or other active malignancy.
  9. Solid organ transplant recipients.
  10. Antibiotic treatment within the previous 3 months.
  11. Suffering from any acute or chronic cardiovascular, GI or immunological condition.
  12. Gastric or duodenal ulcer in the past six months.
  13. Currently pregnant or nursing.
  14. Concomitant diseases with reduced life expectancy.
  15. Combined mental illness.
  16. Contraindication to MRI scanning.
  17. Exclusions may also be made at the discretion of the attending physician or the eligibility committee.
  18. Inability to provide informed consent.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Dietitian led life style modification intervention.
Lifestyle changes supervised by dietitians
All participants received recommendations for a low-fat hypocaloric diet that was 750 kcal/day less than their daily energy need which supervised by dietitians. Additionally, patients were encouraged to walk 200 minutes per weeks and a short self-report questionnaire for the measurement of habitual physical activity was implemented at baseline, 4, 16, 32 and 48 weeks.
Experimental: Conventional care (control)
Receive routine care
Receive routine care

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Hepatic fat
Time Frame: 12 months
Change of liver proton density fat fraction (PDFF) in MAFLD assessed by magnetic resonance imaging (MRI)
12 months
Obesity
Time Frame: 1, 4, 8, 12, 24 months
Changes in body weight
1, 4, 8, 12, 24 months
Gut microbiota
Time Frame: 1, 4, 8, 12, 24 months
Changes in bacterial component of the gut microbiome
1, 4, 8, 12, 24 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Blood pressure
Time Frame: 1, 4, 8, 12, 24 months
Changes in blood pressure
1, 4, 8, 12, 24 months
Central obesity
Time Frame: 1, 4, 8, 12, 24 months
Changes in waist circumference
1, 4, 8, 12, 24 months
Insulin resistance
Time Frame: 1, 4, 8, 12, 24 months
Changes in insulin resistance eveluated by HOMA-IR
1, 4, 8, 12, 24 months
FPG
Time Frame: 1, 4, 8, 12, 24 months
Changes in fast plasma glucose
1, 4, 8, 12, 24 months
HbA1c
Time Frame: 1, 4, 8, 12, 24 months
Changes in HbA1c
1, 4, 8, 12, 24 months
Plasma triglycerides
Time Frame: 1, 4, 8, 12, 24 months
Changes in plasma triglycerides
1, 4, 8, 12, 24 months
Plasma HDL-cholesterol
Time Frame: 1, 4, 8, 12, 24 months
Changes in plasma HDL-cholesterol
1, 4, 8, 12, 24 months
Plasma high-sensitivity C-reactive protein level
Time Frame: 1, 4, 8, 12, 24 months
Changes in plasma high-sensitivity C-reactive protein level
1, 4, 8, 12, 24 months
Gut microbiota diversity
Time Frame: 1, 4, 8, 12, 24 months
Changes in diversity of gut microbiome(α-diversity and β-diversity)
1, 4, 8, 12, 24 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 17, 2020

Primary Completion (Anticipated)

May 17, 2024

Study Completion (Anticipated)

December 30, 2024

Study Registration Dates

First Submitted

April 20, 2021

First Submitted That Met QC Criteria

April 29, 2021

First Posted (Actual)

May 4, 2021

Study Record Updates

Last Update Posted (Actual)

May 4, 2021

Last Update Submitted That Met QC Criteria

April 29, 2021

Last Verified

April 1, 2021

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • NFEC-2019-254

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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