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Completed

NCT Number: NCT05866744

Effects of Time-restricted Hypocaloric Diet in Patients with NAFLD

The effects of a time-restricted hypocaloric Mediterranean type diet compared to a conventional hypocaloric Mediterranean type diet on blood glucose metabolism and liver steatosis in people with non-alcoholic fatty liver disease will be investigated.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Agricultural University of Athens, Athens, Attica, Greece

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About this study

The goal of this clinical trial is to evaluate the effects of the time in which food intake is restricted (morning or evening hours or no restriction in time) on glucose metabolism and liver steatosis in the context of a hypocaloric diet plan in 54 patients with non-alcoholic fatty liver disease (NAFLD). The participants will be divided into 3 groups of 18 individuals each and will be randomly assigned to one of the 3 dietary interventions. In the first group (control group), participants will be given a weight loss program based on the principles of the Mediterranean Diet (energy deficit of 500 kcal/day with the aim of losing 0.5 kg per week) with the instruction to consume their meals throughout the day, without time restriction. In the second group (early eaters), individuals will be given a weight loss program based on the principles of the Mediterranean Diet (energy deficit of 500 kcal/day with the aim of losing 0.5 kg per week), and they will be asked to consume all of their meals within 10 hours (between 07:00-09:00 and 17:00-19:00) and refrain from consuming caloric foods and drinks for the remaining 14 hours. In the third group (late eaters), individuals will be given a weight loss program based on the principles of the Mediterranean Diet (energy deficit of 500 kcal/day with the aim of losing 0.5 kg per week), and they will be asked to consume all of their meals within 10 hours (between 11:00-13:00 and 21:00-23:00) and refrain from consuming caloric foods and drinks for the remaining 14 hours.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Body Mass Index >25 kg/m2
  • Liver steatosis with Magnetic Resonance Elastography (MRE)

Exclusion criteria

  • Other chronic liver diseases
  • Alcohol consumption >20 g/day (female) and >30 g/day (male)
  • Medications that cause liver disease or secondary NAFLD (e.g. tamoxifen, corticosteroids, Methotrexate, tetracycline, estrogens, valproic acid)
  • Changes in body weight ± 3 % in the last 3 months
  • Patients following a hypocaloric diet program and/or time-restricted feeding and/or other intermittent fasting protocols
  • Unstable glucose-lowering medications in the last 6 months
  • Body weight lowering medications and/or history of bariatric surgery
  • Statins and/ or other fat-reducing medications if not taken in steady dosage for at least 3 months
  • Uncontrolled type 2 diabetes mellitus defined as HbA1c value > 9.0% or insulin depending type 1 and 2 diabetes mellitus
  • Pregnancy
  • Lactation
  • Immunologic or inflammatory diseases
  • Depression and other psychiatric diseases
  • Patients working in shifts
  • Cancer

Treatment and study plan

Early Time-Restricted Feeding Plus Hypocaloric Mediterranean Diet

Other

18 patients with NAFLD will be asked to follow an early 14:10 (14 hours fasting and 10 hours feeding) time-restricted (eating between 08:00-18:00) and individualized Mediterranean diet plan with caloric restriction (energy deficit of 500 kcal/day) for 12 weeks

Late Time-Restricted Feeding Plus Hypocaloric Mediterranean Diet

Other

18 patients with NAFLD will be asked to follow a late 14:10 (14 hours fasting and 10 hours feeding) time-restricted (eating between 12:00-22:00) and individualized Mediterranean diet plan with caloric restriction (energy deficit of 500 kcal/day) for 12 weeks

Hypocaloric Mediterranean Diet Without Time Restriction In Feeding

Other

18 patients with NAFLD will be asked to follow an individualized Mediterranean diet plan with caloric restriction (energy deficit of 500 kcal/day) without time restriction in feeding (eating throughout the day) for 12 weeks

Primary outcomes

  1. Change in blood glucose concentrations

    Time frame: 12 weeks

    Clinically significant change in blood glucose concentrations (mg/dL)

Secondary outcomes

  1. Change in body weight

    Time frame: 12 weeks

    Clinically significant change in body weight (kg)

  2. Change in blood insulin concentrations

    Time frame: 12 weeks

    Clinically significant change in blood insulin concentrations (μU/L)

  3. Change in Controlled Attenuation Parameter (CAP)

    Time frame: 12 weeks

    Clinically significant change in CAP (dB/m)

  4. Change in blood lipids levels

    Time frame: 12 weeks

    Clinically significant change in triglycerides (mg/dL), total cholesterol (mg/dL), low-density lipoprotein (mg/dL) and high-density lipoprotein (mg/dl)

  5. Change in Chronic Liver Disease Questionnaire (CLDQ)

    Time frame: 12 weeks

    Clinically significant change in health status within individuals with NAFLD. The CLDQ includes 29 items in the following domains: abdominal symptoms, fatigue, systemic symptoms, activity, emotional function and worry. Overall CLDQ scores calculated for each domain range from 1 (most impaired) to 7 (minimum frequency of symptoms). The total score is calculated as the average score of the 29 items.

Sponsors and collaborators

Lead sponsor

Agricultural University of Athens

Other

Collaborators

  • Laikο General Hospital, Athens

Registry information

Official study title

Effects of a Time-restricted Hypocaloric Mediterranean Diet in Patients with Non-alcoholic Fatty Liver Disease on Glucose Metabolism (CHRONO-NAFLD Project)

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
May 19, 2023
Registry last updated
Oct 30, 2024

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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