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RecruitingNCT05968378Updated Aug 1, 2023

Diet, Immunometabolism and Non-alcoholic Fatty Liver Disease

An interventional study of Standard healthy eating advice and eTRE plus Mediterranean diet in Non-Alcoholic Fatty Liver Disease, Liver Fat and Obesity, sponsored by University College Dublin. Recruiting at 1 site in Ireland. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2023-08-01.

Sponsored by University College Dublin · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Jun 2024, 2 years 4 months ago, but the record still lists the study as recruiting.
  • Started Jun 2023; still recruiting 3 years 4 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

This study will assess the impact of 8-hour time restricted eating (8 hours of eating, 16 hours fasting) combined with a Mediterranean diet on metabolism and inflammation in adults with non-alcoholic fatty liver disease (NAFLD).

Read the detailed description

Non-alcoholic fatty liver disease (NAFLD), defined as the accumulation of fat in the liver that is not related to alcohol intake, is the number 1 global cause of chronic liver disease. Excessive consumption of energy, saturated fat, and simple sugars is a key contributor to hepatic lipid accumulation and obesity-induced metabolic inflammation, reflecting cross-talk between immune and metabolic pathways. Moreover, dietary factors including saturated fatty acids, cholesterol, and their derivatives, as well as gut-derived metabolites, can prime innate immune cells to induce an exaggerated pro-inflammatory response upon re-exposure to such stimuli and may contribute to chronic low grade inflammation.

Dietary strategies focusing on replacing inflammatory dietary triggers with monounsaturated fats, fiber and complex carbohydrates have been shown to improve metabolic dysfunction, but how this relates to a rewiring of the innate immune system is less clear. Time-restricted eating (TRE) is another dietary strategy which has been shown to elicit beneficial effects that reduce the risk of chronic metabolic disease and consolidates eating to a 6-10 hour period daily. Early TRE (eTRE), wherein eating occurs from morning to early afternoon, is associated with greater cardiometabolic health benefits than eating late in the evening. This includes improved insulin sensitivity, glucose tolerance and lipid metabolism, and reduced inflammatory markers.

This study will determine the impact of an 8-week intervention of 8-hour eTRE combined with an anti-inflammatory Mediterranean diet on the metabolic and immune phenotype of individuals with NAFLD, a population at high risk of progressive cardiometabolic decline and chronic inflammation. By focusing on improving both nutrient quality and nutrient timing, a greater understanding of the interaction between systemic metabolism and immune cell rewiring will be gained.

02

Conditions studied

  • Non-Alcoholic Fatty Liver Disease
  • Liver Fat
  • Obesity
  • Inflammation
03

In context

Liver Diseases

2,081 studies on the registry are indexed under Liver Diseases; 390 are open to participants now.

This study's planned enrollment of 60 is above the median of 50 across 1,323 interventional studies indexed under Liver Diseases.

Browse Liver Diseases studies →

Lead sponsor

University College Dublin is the lead sponsor of 108 studies on the registry; 31 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Males and females
  • Age 18-65 years, from all ethnic groups, capable of providing informed consent to participate
  • Obesity (body mass index >30kg/m\^2) and of stable body weight (±3% for ≥3 months)
  • Fasting blood glucose \<7.0 mmol/L and HbA1c \<6.5%.
  • Liver fat >10% (CAP score >238 dB/m) and no fibrosis (liver stiffness score 2-7 kPa) as assessed by liver elastography (FibroScan)

Exclusion criteria

Exclusion Criteria:

  • Impaired renal function
  • Abnormal hematocrit
  • History of cardiovascular events
  • Uncontrolled hypertension
  • Type 2 diabetes
  • Medications or supplements known to affect glucose or lipid metabolism
  • Active inflammatory, autoimmune, infectious, gastrointestinal, or malignant disease
  • Uncontrolled neurological or psychiatric disease
  • Iron deficiency anemia, (hemoglobin \< 12g/dl men, \< 11g/dl women)
  • Fatty acid supplements and consumers of high doses of anti- antioxidant vitamins (A, C, E, b-carotene)
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
60 participants (estimated)

Study arms

  • Active comparator
    Standard healthy eating advice

    Subjects in this group will be counselled according to the Irish National Healthy Eating Guidelines.

    Behavioral: Standard healthy eating advice

  • Experimental
    eTRE plus Mediterranean diet

    Subjects in this group will be asked to restrict their eating to 8-hours daily (8am - 4pm) and to adhere to a Mediterranean style diet.

    Behavioral: eTRE plus Mediterranean diet

Interventions

  • BehavioralStandard healthy eating advice

    Subjects in this group will be provided with standard healthy eating advice according to the Irish National Healthy Eating Guidelines and Food Pyramid and will be asked to follow this advice for 8-weeks.

  • BehavioraleTRE plus Mediterranean diet

    Subjects in this group will be asked to consume all meals between 8am - 4pm and to adhere to a Mediterranean style diet daily for 8-weeks.

06

What researchers measure

Primary outcomes

  1. Change in plasma inflammatory response to a high-fat meal: C-reactive protein (CRP)

    Postprandial changes in CRP (mg/L) will be measured in response to a high-fat meal

    Time frame: To be assessed at baseline and post 8-week intervention

  2. Change in plasma inflammatory response to a high-fat meal: Interleukin-6 (IL-6)

    Postprandial changes in IL-6 (pg/mL) will be measured in response to a high-fat meal

    Time frame: To be assessed at baseline and post 8-week intervention

  3. Change in plasma inflammatory response to a high-fat meal: Interleukin-1-beta (IL-1β)

    Postprandial changes in IL-1β (pg/mL) will be measured in response to a high-fat meal

    Time frame: To be assessed at baseline and post 8-week intervention

  4. Change in plasma inflammatory response to a high-fat meal: Tumor necrosis factor alpha (TNF-α)

    Postprandial changes in (TNF-α) (pg/mL) will be measured in response to a high-fat meal

    Time frame: To be assessed at baseline and post 8-week intervention

Secondary outcomes

  1. Change in metabolic response to a high-fat meal: Glucose

    Plasma glucose (mg/dL) response to a high-fat meal will be assessed

    Time frame: To be assessed at baseline and post 8-week intervention

  2. Change in metabolic response to a high-fat meal: Insulin

    Plasma insulin (μU/mL) response to a high-fat meal will be assessed

    Time frame: To be assessed at baseline and post 8-week intervention

  3. Change in metabolic response to a high-fat meal: Glucagon

    Plasma glucagon (pg/mL) response to a high-fat meal will be assessed

    Time frame: To be assessed at baseline and post 8-week intervention

  4. Change in metabolic response to a high-fat meal: Triglycerides

    Plasma triglycerides (mg/dL) response to a high-fat meal will be assessed

    Time frame: To be assessed at baseline and post 8-week intervention

  5. Change in metabolic response to a high-fat meal: Non-esterified fatty acids (NEFA)

    Plasma NEFA (mmol/L) response to a high-fat meal will be assessed

    Time frame: To be assessed at baseline and post 8-week intervention

  6. Innate immune function

    8-week change in innate immune function will be assessed ex-vivo using whole blood simulation assay.

    Time frame: To be assessed at baseline and post 8-week intervention

  7. Innate immune training

    8-week change in innate immune function will be assessed in isolated monocytes stimulated with beta glucan and restimulated with lipopolysaccharide.

    Time frame: To be assessed at baseline and post 8-week intervention

  8. Insulin resistance

    8-week change in insulin resistance using Homeostatic Model Assessment for Insulin Resistance (HOMA-IR).

    Time frame: To be assessed at baseline and post 8-week intervention

  9. Adipose tissue insulin resistance

    8-week change in adipose tissue insulin resistance using the adipose tissue insulin resistance index (Adipo-IR).

    Time frame: To be assessed at baseline and post 8-week intervention

  10. Change in intrahepatic triglyceride content

    Liver elastography (FibroScan) will be used to determine change in liver fat after the 8-week intervention.

    Time frame: To be assessed at baseline and post 8-week intervention

  11. Change in liver stiffness measurement

    Liver elastography (FibroScan) will be used to determine change in liver stiffness after the 8-week intervention.

    Time frame: To be assessed at baseline and post 8-week intervention

  12. HDL Proteome

    8-week change in the composition of the HDL proteome.

    Time frame: To be assessed at baseline and post 8-week intervention

  13. Body weight

    8-week change in body weight in kilograms

    Time frame: To be assessed at baseline and post 8-week intervention

  14. Body mass index (BMI)

    8-week change in BMI

    Time frame: To be assessed at baseline and post 8-week intervention

  15. Body fat percentage

    8 week change in body fat percentage using bioelectrical impedance analysis

    Time frame: To be assessed at baseline and post 8-week intervention

  16. Waist and hip circumferences

    8-week change in waist and hip circumference measured in centimeters using a body tape measure

    Time frame: To be assessed at baseline and post 8-week intervention

  17. Gut microbiome composition and function

    8-week functional changes in gut microbiome will be assessed by integrating 16S sequencing of fecal samples with fecal water metabolomics.

    Time frame: To be assessed at baseline and post 8-week intervention

  18. Dietary intake

    8-week change in dietary intake using a 3-day semi-weighed food diary.

    Time frame: To be assessed at baseline and post 8-week intervention

  19. Physical activity level (PAL)

    8-week change in PAL using the International Physical Activity Questionnaire - Short form (IPAQ-SF). This form has 7 questions about time spent doing physical activity(leisure time, work, domestic tasks, and travel) in the last 7 days. Activities are grouped according to vigorous or moderate intensity, and walking. Each intensity is assigned a metabolic equivalent (MET). The time spent at each intensity is used to estimate weekly physical activity using the associated METs. Minimum and maximum values are 0 and 154,224 METs. Classification as 'sufficiently active' requires ≥600 METs/week which may be achieved through a combination of intensities. Classification as 'highly active' requires: a) vigorous-intensity activity on ≥3 days achieving a minimum of ≥1500 METs/week OR b) ≥7 days of any combination of walking, moderate-intensity or vigorous-intensity activities achieving ≥ 3000 METs/week. A physical activity level below these categories is undesirable.

    Time frame: To be assessed at baseline and post 8-week intervention

  20. Mediterranean diet adherence

    8-week change in Mediterranean diet adherence score using the PREDIMED 14-item Mediterranean Diet Assessment Tool. This questionnaire is used to assess adherence to the traditional Mediterranean Diet. Two of the 14 questions relate to the use of olive oil, a key component of the Mediterranean Diet, and 12 questions relate to the consumption of foods which characterize the Mediterranean Diet. Each item has a criteria which must be met to achieve 1 point e.g., at least 3 pieces of fruit daily. The minimum score is 0 and the maximum is 14, where a score of ≤ 5 indicates low adherence, 6-9 moderate adherence, and \> 9 high adherence.

    Time frame: To be assessed at baseline and post 8-week intervention

07

Study locations

1 of 1 sites recruiting
  • University College Dublin
    Dublin, Leinster D04 V1W8, Ireland
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 1, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05968378
Lead sponsor
University College Dublin
Collaborators
St. James's Hospital, Ireland
Responsible party
Sponsor
First posted
Aug 1, 2023
Start date
Jun 1, 2023
Primary completion
Jun 2024 (estimated)
Completion
Jul 2024 (estimated)
Last update
Aug 1, 2023

Study contacts

Helen M Roche, Professor
Contact
helen.roche@ucd.ie
+353017164031
Christopher E Shannon, PhD
Contact
christopher.shannon@ucd.ie

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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