ObesityCALIBRATENCT04786418
Low-Calorie Diet in People With Prediabetes/Metabolic Syndrome
A study testing Low-calorie diet in people with Obesity and NAFLD, run by University of Liverpool at 1 site in United Kingdom.
Trial summary
Significant weight reduction, achieved by low-calorie diet (LCD), will mobilise ectopic fat (visceral and particularly liver fat), improving insulin sensitivity and other metabolic syndrome components, with secondary beneficial effects on cardiac structure and function. Read more about this study
- Who is it for?
- Ages 18 to 55 yearsHealthy volunteers can take part
- Conditions the study is for
- Obesity, NAFLD, Fatty Liver
- What is being tested?
- Low-calorie diet
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 44 participants
- Where
- 1 siteUnited Kingdom
- Study dates
- 1 Jun 2021to 31 Dec 2024
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 55 years
- All sexes
- Healthy volunteers accepted
- Adult
Who may be able to join
- The investigators shall recruit participants with the following characteristics:
- Men and women
- aged 18-55 years*,
- BMI 30-40 kg/m2 , BMI>27 kg/m2 for Chinese/South Asians
- Any one of the following three metabolic criteria:
- a diagnosis of prediabetes (HbA1c 42-47 mmol/mol), OR
- NAFLD (based on fatty liver index, FLI >60). FLI will be determined using waist circumference, BMI, serum triglyceride and GGT (gamma-glutamyltransferase). OR
- a diagnosis of metabolic syndrome using the IDF metabolic syndrome criteria (see below,
Who cannot join
- Individuals with normal glucose tolerance (NGT) or type 1 or type 2 diabetes (T2D).
- Anyone engaged in active weight loss (>5kg weight loss in the last 6 months), currently engaged with weight management service, previous bariatric surgery, on weight-lowering medications (e.g. orlistat or liraglutide) or with a history of an eating disorder.
- planning pregnancy/6 months post-partum,
- known structural cardiac disease or anyone with major atherosclerotic disease
- history of stroke within the last 3 months
- Active mental health illness (e.g. severe depression, bipolar disorder, schizophrenia or other psychotic disorders). Use of drug with known major effects on bodyweight (e.g. corticosteroid, anti-psychotic, anticonvulsants etc).
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- Planning pregnancy within the next 6 months and until >6 months post-partum or breastfeeding
- Substance abuse e.g. drugs/alcohol.
- Eating disorder, previous bariatric surgery, currently taking weight loss drugs or already engaged with weight management service
- Learning difficulties
- A contraindication to magnetic resonance scanning will exclude the patient from the MRI component of the study
Trial locations and contacts
1 site in 1 country.
United Kingdom1 site
Liverpool University Hospital NHS Foundation Trust are an NHS organisation
Liverpool, L97AL
About this study
Official title: Metabolic, Multi-organ and Microvascular Effects of a Low-calorIe Diet in Younger Obese With Prediabetes and/or Metabolic Syndrome
Significant weight reduction, achieved by low-calorie diet (LCD), will mobilise ectopic fat (visceral and particularly liver fat), improving insulin sensitivity and other metabolic syndrome components, with secondary beneficial effects on cardiac structure and function.
This CALIBRATE study (metabolic, multi-organ and effects of low-calorie diet in younger obese patients with pre-diabetes) will compare the effects of a safe and effective 12-month weight management intervention, initially using a low-calorie, liquid replacement diet for 12 weeks, anticipating at least 10% reduction in body weight. The investigators will examine how much the weight loss improves the metabolic abnormalities that precede type 2 diabetes (T2D), and in reversing the pre-clinical/subtle clinical abnormalities of the liver and heart that precede liver and cardiovascular disease (CVD).
This study will compare the effects of a safe and effective 12-month weight management intervention, initially using a low-calorie, liquid replacement diet for 12 weeks, followed by a weight maintenance phase. The investigators will examine how much the weight loss improves the metabolic and neuropathic abnormalities that precede and accompany type 2 diabetes (T2D), and in reversing the pre-clinical/subtle clinical abnormalities of the liver and heart that precede liver and cardiovascular disease. In an additional optional sub-study, the investigators will additionally assess how the weight loss impacts upon appetite regulation within the brain with functional MRI (fMRI).
Read the detailed description
Prediabetes affects up to 35% of the population. It is defined as an intermediate metabolic state of glucose dysregulation between normoglycaemia and type 2 diabetes (T2D). Prediabetic individuals have 3-12 times higher annual incidence of type 2 diabetes than the general population. Further, these individuals have a considerable increased risk of cardiovascular disease (CVD), (myocardial infarction, stroke, CV death) and even in the absence of coronary artery disease, an increased risk of heart failure. Individuals with prediabetes manifest the same clustering of cardiovascular risk factors (dysglycaemia, dyslipidaemia, hypertension, obesity, physical inactivity, insulin resistance, pro-coagulant state, endothelial dysfunction, inflammation) that confer the high risk for macrovascular complications in type 2 diabetes. For example, 37% and 51% of individuals with prediabetes have hypertension and dyslipidaemia.
Results of large randomised control trials focusing on diabetes management have shown improvements in cardiovascular and renal outcomes and treatments for patients with established type 2 diabetes. Studies examining cardiovascular and renal burdens in patients with prediabetes have demonstrated that the same therapeutic benefits have not been observed in adults with prediabetes. This study focuses on a younger age group considering the aggressive phenotype of young-onset type 2 diabetes as it provides the opportunity to address and effectively manage the associated cardio-metabolic risk factors, prevent progression from prediabetes to type 2 diabetes and reduce the burden of cardiovascular disease, heart failure and liver-related burden.
Liver fat predicts both cardiovascular disease and type 2 diabetes independent of obesity. NAFLD is a growing clinical problem which has become the most prevalent chronic liver disease in Western society. It can be associated with isolated hepatic triglyceride accumulation (steatosis), through steatosis plus hepatocellular damage with inflammation and fibrosis (non-alcoholic steatohepatitis (NASH), which may ultimately progress to liver fibrosis/cirrhosis and hepatocellular carcinoma.
Non-Alcoholic Fatty Liver Disease (NAFLD) is considered the hepatic manifestation of the metabolic syndrome and is commonly associated with insulin-resistant states including obesity, a higher prevalence of prediabetes and type 2 diabetes (T2D).
NAFLD has a bi-directional relationship with prediabetes and T2D being a risk factor for Non-Alcoholic Fatty Liver Disease but conversely, individuals with prediabetes and type 2 diabetes have significantly increased liver fat versus non-diabetic control subjects with a higher risk of NAFLD than Body Mass Index (BMI) -matched non-diabetic controls.
NAFLD is associated with a metabolic phenotype similar to that observed in T2D: hepatic and peripheral insulin resistance with reduced skeletal muscle glucose uptake and increased non-esterified fatty acid (NEFA) release from adipose tissue lipolysis. Once liver fat accumulates in the liver, insulin is unable to inhibit glucose and very-low-density lipoprotein (VLDL) production resulting in overproduction of glucose and very-low-density lipoprotein (VLDL) particles leading to hypertriglyceridaemia and low high-density lipoprotein (HDL)-cholesterol concentrations.
NAFLD is associated with an increased risk of cardiovascular disease with CVD now representing the leading cause of death in NAFLD. While it remains contentious whether the increased risk of CVD in NAFLD is explained by the combination of common risk factors shared by both NAFLD and CVD, most epidemiological studies evaluating CVD risk in NAFLD suggest the risk occurs independently of associated risk factors. These studies have relied upon biochemical and imaging surrogate markers of NAFLD (e.g. serum liver enzymes, abdominal ultrasound). Using more detailed assessment of NAFLD e.g. assessment of fibrosis with fibrosis panels, with Magnetic Resonance Imaging (MRI) or even biopsy-based.
Clinical studies have shown that sustained moderate weight loss of around 5-10%, achieved through lifestyle intervention lowers blood pressure, improves glucose control, prevents diabetes, and improves dyslipidaemia, as well as improving haemostatic and fibrinolytic factors. The effects of weight reduction on progression to T2D has been studied in pre-diabetes in the Diabetes Prevention Programme study (US) study. A 1 kg of weight loss is associated with a 16% reduction in the progression of pre-diabetes to T2D.
Metabolic surgery is associated with remission of T2D. There is overwhelming evidence that LCDs have a useful role in T2D resulting in substantial weight loss (mean difference in weight vs. controls after 3 months was 7.38 kg (CI: 16.2, 1.5) with high levels of adherence. They can potentially cause profound weight loss of 15-20% of body weight in severe and medically complicated obesity. The weight loss is associated with significant reductions in hepatic and pancreatic fat with associated improvements in insulin sensitivity and pancreatic ß-cell function resulting in remission of T2D in many cases. This dramatic dietary intervention, initially believed to be unmanageable and difficult to maintain, has been demonstrated to be implementable and highly efficacious even when delivered through primary care settings.
In one primary care study, using LCD in T2D patients recorded a weight loss of 15kg or more in 24% of patients after 12 months. It is unsurprising that 46% of the participants achieved remission of their T2D. LCD produces bariatric type weight loss and improves glycaemic control in diabetes and results in remission of T2D in the majority of patients, however the impact on complications, remains to be determined particularly in obese people without diabetes. One non-pharmacological strategy to improve cardio-metabolic health in obesity, pre-diabetes and type 2 diabetes mellitus (T2DM) includes the application of a low-calorie diet (LCD), utilising reduced daily energy intake (<800kcal).
To this extent, the purpose of this study is to examine the impact of intensive weight management on metabolic, liver and cardiac health, measures on neuropathy and on appetite regulation. The investigators will study younger (<55y) obese people with pre-diabetes and/or metabolic syndrome who exhibit early or pre-clinical evidence of metabolic and cardiovascular complications. The investigators will investigate the effects of a low-calorie diet (LCD) as one of the most effective and least invasive mechanism by which these various factors can be improved.
- Conditions
- Obesity, NAFLD, Fatty Liver, Pre Diabetes, Metabolic Syndrome
- Being tested
- Standard of care, Low-calorie diet
- Keywords
- Obesity, Metabolic Syndrome, Pre Diabetes, NAFLD, Fatty Liver, Low-calorie diet, functional magnetic resonance imaging, skin biopsy, appetite regulation
- Medical subject headings
- Obesity, Non-alcoholic Fatty Liver Disease, Fatty Liver, Glucose Intolerance, Metabolic Syndrome
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Standard of careOther
Participants allocated to the control group will be given standard clinical information regarding healthy eating, physical activity and management of weight, in line with current NHS practise.
Low-calorie dietDietary supplement
The LCD intervention group, will received a well validated, commercially available, intensive weight management protocol Counterweight-Plus.
| Study group | Role | What they receive |
|---|---|---|
| Control group | Active comparator | Participants will be given standard advice about healthy eating, physical activity and management of weight during the study visit, in line with current NHS practice. There will be a total of 9 study visits for this group. Receives: Other: Standard of care |
| Low-calorie diet intervention group | Experimental | Participants will received a special diet involving 25 regular visits and intensive management. Participants will be given a supply of especially formulated soups and shakes, a special diet in a form of powder that need to be mixed with 200 ml water. Receives: Dietary Supplement: Low-calorie diet |
What is being measured
The primary outcome is the main question the study is designed to answer.
Changes in liver fat >5 percent, determined by MRI, from baseline to after 12 months of intervention.
For liver fat, diagnosis of NAFLD is based on a threshold of a value >5.5 percent. The investigators anticipate having a 45 percent difference in the proportion in whom liver fat percentage reduces by at least 5 percent between the groups (50 percent of LCD will have an absolute reduction in liver fat of 5 percent vs. 5 percent of controls). The investigators chose an absolute reduction of liver fat of 5 percent as this reduction is clinically meaningful.
Measured: Changes will be measured at baseline and at 12 months.
Secondary outcomes (30)
Body Mass Index
Weight (kg) and height (cm) to measure body mass index (BMI) and to assess the changes in body mass index (BMI).
Measured: Changes will be measured at baseline and at 12 months.
Body weight
Body weight (kg) and to assess the changes in body weight (kg).
Measured: Changes will be measured at baseline and at 12 months.
Waist Circumference
To access changes of waist circumference that is correlated with visceral (abdominal) adiposity (cm).
Measured: Changes will be measured at baseline and at 12 months.
Blood pressure
Systolic and Diastolic (mmHg)
Measured: Changes will be measured at baseline and at 12 months.
Liver biochemistry: Alanine transaminase
To access liver function tests of ALT (u/L).
Measured: Changes will be measured at baseline and at 12 months.
Changes in HbA1c
Changes of HbA1c of 6 mmol/mol in approximately 50 percent of the LCD intervention group vs. 5 percent in the control group. The investigators believe the application of thresholds in looking at the changes in HbA1c are justified based on the diagnostic thresholds used in the diagnosis of normal glucose tolerance (NGT) (HbA1c<42 mmol/mol), prediabetes (42-47 mmol/mol) and type 2 diabetes (T2D) (>48 mmol/mol). By using a threshold of HbA1c reduction of 6 mmol/mol, all participants, irrespective of their baseline HbA1c would have remission of prediabetes to NGT. The investigators avoided categorising individuals as moving from prediabetes to NGT would capture small changes in HbA1c that were less clinically significant (e.g. an individual who goes from 43 to 41 mmol/mol).
Measured: Changes will be measured at baseline, at 12 weeks, at 24 week and at 12 months.
Lipid profile
LDL, HDL, total cholesterol and triglycerides (mmol/L)
Measured: Changes will be measured at baseline and at 12 months.
Metabolic measures of fatty liver
Fatty liver index (FLI) score:
<30/Low/Fatty liver ruled out (LR- = 0.2)
30 to <60/Indeterminate/Fatty liver neither ruled in nor ruled out
≥60/High/Fatty liver ruled in (LR+ = 4.3)
Measured: Changes will be measured at baseline and at 12 months.
Markers of fibrosis in liver
FIB-4 Score (Approximate fibrosis stage*) <1.45 = 0-1
1.45-3.25 = 2-3
3.25 = 4-6
Measured: Changes will be measured at baseline and at 12 months.
The NAFLD scoring screening tool
NAFLD fibrosis score
= -1.675 + 0.037 × age (years) + 0.094 × BMI (kg/m2) + 1.13 × IFG/diabetes (yes = 1, no = 0) + 0.99 × AST/ALT ratio - 0.013 × platelet (×109/l) - 0.66 × albumin (g/dl).
< -1.455: predictor of absence of significant fibrosis (F0-F2 fibrosis) ≤ -1.455 to ≤ 0.675: indeterminate score 0.675: predictor of presence of significant fibrosis (F3-F4 fibrosis)
Measured: Changes will be measured at baseline and at 12 months.
Peripheral insulin sensitivity
Oral Glucose Tolerance Test (mmol/L)
Measured: Changes will be measured at baseline and at 12 months.
Changes in hepatic insulin sensitivity
Hepatic insulin sensitivity
Measured: Changes will be measured at baseline and at 12 months.
Changes in insulin secretion
Pancreatic beta cell function
Measured: Changes will be measured at baseline and at 12 months..
Changes in fatty acid metabolism
Fatty acid handling
Measured: Changes will be measured at baseline and at 12 months.
Measures of neuropathy: Change in intra-epidermal nerve fibres densities, length and branch densities.
- Change in corneal nerve fibre density (CNFD) - Number of major nerves/ mm2 of corneal tissue.
- Change in corneal nerve fibre length (CNFL) - Length of nerves/ mm2 of corneal tissue.
- Change in corneal nerve branch density (CNBD) - Number of nerve branches/mm2 of corneal tissue.
Measured: Changes will be measured at baseline and at 12 months.
Measures of neuropathy: Change in sural nerve velocity
Velocity (m/s)
Measured: Changes will be measured at baseline and at 12 months.
Measures of neuropathy: Change in sural nerve amplitude
Amplitude (mV)
Measured: Changes will be measured at baseline and at 12 months.
Functional MRI
Changes in brain signals in response to food cues
Measured: Changes will be measured at baseline and at 12 months.
Appetite measurement
Visual Analog Score for Appetite: Scale range from 0 to 10 (not at all to extremely)
Hungry : 0 (Not at all hungry) - 10 (Extremely hungry)
Fullness: 0 (Not at all full) - 1- (Extremely full)
Satisfied: 0 (Not at all satisfied) - 10 (Extremely satisfied)
Strong desire to eat: 0 (not at all strong) - 10 (Extremely strong)
How much food you could eat : 0 (Not at all) - 10 (a large amount)
Thirsty: 0( not at all thirsty) - 10 (Extremely thirsty)
Nauseous: 0 (not at all nauseous) - 10 (Extremely nauseous)
Measured: Changes will be measured at baseline and at 12 months.
MRI-derived fat volumes
Subcutaneous and visceral fat content (litres)
Measured: Changes will be measured at baseline and at 12 months.
Cardiac structure (volumes)
Cardiac chamber volumes at various phases in cardiac cycle (LVESV, LVEDV)
Measured: Changes will be measured at baseline and at 12 months.
Cardiac health: cardiac magnetic resonance imaging
LV mass (g)
Measured: Changes will be measured at baseline and at 12 months.
Cardiac health: LV Mass Indexed to Body Surface Area
LV Mass Indexed to Body Surface Area (g/m2)
Measured: Changes will be measured at baseline and at 12 months.
Cardiac health: Multi-parametric cardiac MRI
LV Mass: volume ratio (LVM/LVEDV)
Measured: Changes will be measured at baseline and at 12 months.
Changes in early diastolic strain rate by cardiovascular magnetic resonance
Peak early diastolic strain rate (s-1)
Measured: Changes will be measured at baseline and at 12 months.
Changes in load and contractility of the cardiac function
Peak systolic strain (percent)
Measured: Changes will be measured at baseline and at 12 months.
Charcterisation of organ fat content
Liver, pancreas, kidney, skeletal muscle
Measured: Changes will be measured at baseline and at 12 months.
Multi-organ MRI measure for pancreas, spleen and kidney
Fibrosis score cT1 (ms)
Measured: Changes will be measured at baseline and at 12 months.
Multi organs pancreas, spleen and kidney volume
Volumes (cm3)
Measured: Changes will be measured at baseline and at 12 months.
Multi organs pancreas, spleen and kidney fat content
Fat content (percent)
Measured: Changes will be measured at baseline and at 12 months.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted8 Mar 2021
- Study start1 Jun 2021
- Primary completion31 Dec 2024
- Study completion31 Dec 2024
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for ObesityStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- There are two study groups: Control groups and low-calorie diet intervention group running alongside.
- Masking
- None (open label)
- Enrolment
- 44 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Liverpool
- Sponsor type
- University, hospital or other
- Collaborators
- University of Surrey, Perspectum
- Responsible party
- Sponsor
- Investigators
- Daniel Cuthbertson, Principal investigator, University of Liverpool
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04786418
- Sponsor's protocol ID
- UoL001503
- Acronym
- CALIBRATE
- Status last verified
- Jun 2025
- First submitted
- 21 Jan 2021
- Last updated
- 27 Jun 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Leslie WS, Ford I, Sattar N, Hollingsworth KG, Adamson A, Sniehotta FF, McCombie L, Brosnahan N, Ross H, Mathers JC, Peters C, Thom G, Barnes A, Kean S, McIlvenna Y, Rodrigues A, Rehackova L, Zhyzhneuskaya S, Taylor R, Lean ME. The Diabetes Remission Clinical Trial (DiRECT): protocol for a cluster randomised trial. BMC Fam Pract. 2016 Feb 16;17:20. doi: 10.1186/s12875-016-0406-2.
PubMed 26879684
Study at a glance
From the registry record, last updated by the sponsor on 27 Jun 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Metabolic, Multi-organ and Microvascular Effects of a Low-calorIe Diet in Younger Obese With Prediabetes and/or Metabolic Syndrome
- ClinicalTrials.gov ID
- NCT04786418
- Acronym / sponsor ID
- CALIBRATE / UoL001503
- Conditions
- Obesity, NAFLD, Fatty Liver, Pre Diabetes, Metabolic Syndrome
- Keywords
- Obesity, Metabolic Syndrome, Pre Diabetes, NAFLD, Fatty Liver, Low-calorie diet, functional magnetic resonance imaging, skin biopsy
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 44 participants (actual)
- Lead sponsor
- University of LiverpoolUniversity, hospital or other
- Collaborators
- University of Surrey, Perspectum
- Study start
- 1 Jun 2021 (actual)
- Primary completion
- 31 Dec 2024 (actual)
- Study completion
- 31 Dec 2024 (actual)
- First posted
- 8 Mar 2021 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Significant weight reduction, achieved by low-calorie diet (LCD), will mobilise ectopic fat (visceral and particularly liver fat), improving insulin sensitivity and other metabolic syndrome components, with secondary beneficial effects on cardiac structure and function.
This CALIBRATE study (metabolic, multi-organ and effects of low-calorie diet in younger obese patients with pre-diabetes) will compare the effects of a safe and effective 12-month weight management intervention, initially using a low-calorie, liquid replacement diet for 12 weeks, anticipating at least 10% reduction in body weight. The investigators will examine how much the weight loss improves the metabolic abnormalities that precede type 2 diabetes (T2D), and in reversing the pre-clinical/subtle clinical abnormalities of the liver and heart that precede liver and cardiovascular disease (CVD).
This study will compare the effects of a safe and effective 12-month weight management intervention, initially using a low-calorie, liquid replacement diet for 12 weeks, followed by a weight maintenance phase. The investigators will examine how much the weight loss improves the metabolic and neuropathic abnormalities that precede and accompany type 2 diabetes (T2D), and in reversing the pre-clinical/subtle clinical abnormalities of the liver and heart that precede liver and cardiovascular disease. In an additional optional sub-study, the investigators will additionally assess how the weight loss impacts upon appetite regulation within the brain with functional MRI (fMRI).
Detailed description
Prediabetes affects up to 35% of the population. It is defined as an intermediate metabolic state of glucose dysregulation between normoglycaemia and type 2 diabetes (T2D). Prediabetic individuals have 3-12 times higher annual incidence of type 2 diabetes than the general population. Further, these individuals have a considerable increased risk of cardiovascular disease (CVD), (myocardial infarction, stroke, CV death) and even in the absence of coronary artery disease, an increased risk of heart failure. Individuals with prediabetes manifest the same clustering of cardiovascular risk factors (dysglycaemia, dyslipidaemia, hypertension, obesity, physical inactivity, insulin resistance, pro-coagulant state, endothelial dysfunction, inflammation) that confer the high risk for macrovascular complications in type 2 diabetes. For example, 37% and 51% of individuals with prediabetes have hypertension and dyslipidaemia.
Results of large randomised control trials focusing on diabetes management have shown improvements in cardiovascular and renal outcomes and treatments for patients with established type 2 diabetes. Studies examining cardiovascular and renal burdens in patients with prediabetes have demonstrated that the same therapeutic benefits have not been observed in adults with prediabetes. This study focuses on a younger age group considering the aggressive phenotype of young-onset type 2 diabetes as it provides the opportunity to address and effectively manage the associated cardio-metabolic risk factors, prevent progression from prediabetes to type 2 diabetes and reduce the burden of cardiovascular disease, heart failure and liver-related burden.
Liver fat predicts both cardiovascular disease and type 2 diabetes independent of obesity. NAFLD is a growing clinical problem which has become the most prevalent chronic liver disease in Western society. It can be associated with isolated hepatic triglyceride accumulation (steatosis), through steatosis plus hepatocellular damage with inflammation and fibrosis (non-alcoholic steatohepatitis (NASH), which may ultimately progress to liver fibrosis/cirrhosis and hepatocellular carcinoma.
Non-Alcoholic Fatty Liver Disease (NAFLD) is considered the hepatic manifestation of the metabolic syndrome and is commonly associated with insulin-resistant states including obesity, a higher prevalence of prediabetes and type 2 diabetes (T2D).
NAFLD has a bi-directional relationship with prediabetes and T2D being a risk factor for Non-Alcoholic Fatty Liver Disease but conversely, individuals with prediabetes and type 2 diabetes have significantly increased liver fat versus non-diabetic control subjects with a higher risk of NAFLD than Body Mass Index (BMI) -matched non-diabetic controls.
NAFLD is associated with a metabolic phenotype similar to that observed in T2D: hepatic and peripheral insulin resistance with reduced skeletal muscle glucose uptake and increased non-esterified fatty acid (NEFA) release from adipose tissue lipolysis. Once liver fat accumulates in the liver, insulin is unable to inhibit glucose and very-low-density lipoprotein (VLDL) production resulting in overproduction of glucose and very-low-density lipoprotein (VLDL) particles leading to hypertriglyceridaemia and low high-density lipoprotein (HDL)-cholesterol concentrations.
NAFLD is associated with an increased risk of cardiovascular disease with CVD now representing the leading cause of death in NAFLD. While it remains contentious whether the increased risk of CVD in NAFLD is explained by the combination of common risk factors shared by both NAFLD and CVD, most epidemiological studies evaluating CVD risk in NAFLD suggest the risk occurs independently of associated risk factors. These studies have relied upon biochemical and imaging surrogate markers of NAFLD (e.g. serum liver enzymes, abdominal ultrasound). Using more detailed assessment of NAFLD e.g. assessment of fibrosis with fibrosis panels, with Magnetic Resonance Imaging (MRI) or even biopsy-based.
Clinical studies have shown that sustained moderate weight loss of around 5-10%, achieved through lifestyle intervention lowers blood pressure, improves glucose control, prevents diabetes, and improves dyslipidaemia, as well as improving haemostatic and fibrinolytic factors. The effects of weight reduction on progression to T2D has been studied in pre-diabetes in the Diabetes Prevention Programme study (US) study. A 1 kg of weight loss is associated with a 16% reduction in the progression of pre-diabetes to T2D.
Metabolic surgery is associated with remission of T2D. There is overwhelming evidence that LCDs have a useful role in T2D resulting in substantial weight loss (mean difference in weight vs. controls after 3 months was 7.38 kg (CI: 16.2, 1.5) with high levels of adherence. They can potentially cause profound weight loss of 15-20% of body weight in severe and medically complicated obesity. The weight loss is associated with significant reductions in hepatic and pancreatic fat with associated improvements in insulin sensitivity and pancreatic ß-cell function resulting in remission of T2D in many cases. This dramatic dietary intervention, initially believed to be unmanageable and difficult to maintain, has been demonstrated to be implementable and highly efficacious even when delivered through primary care settings.
In one primary care study, using LCD in T2D patients recorded a weight loss of 15kg or more in 24% of patients after 12 months. It is unsurprising that 46% of the participants achieved remission of their T2D. LCD produces bariatric type weight loss and improves glycaemic control in diabetes and results in remission of T2D in the majority of patients, however the impact on complications, remains to be determined particularly in obese people without diabetes. One non-pharmacological strategy to improve cardio-metabolic health in obesity, pre-diabetes and type 2 diabetes mellitus (T2DM) includes the application of a low-calorie diet (LCD), utilising reduced daily energy intake (<800kcal).
To this extent, the purpose of this study is to examine the impact of intensive weight management on metabolic, liver and cardiac health, measures on neuropathy and on appetite regulation. The investigators will study younger (<55y) obese people with pre-diabetes and/or metabolic syndrome who exhibit early or pre-clinical evidence of metabolic and cardiovascular complications. The investigators will investigate the effects of a low-calorie diet (LCD) as one of the most effective and least invasive mechanism by which these various factors can be improved.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- There are two study groups: Control groups and low-calorie diet intervention group running alongside.
| Arm | Type | Receives |
|---|---|---|
| Control group | Active comparator | Other: Standard of careParticipants will be given standard advice about healthy eating, physical activity and management of weight during the study visit, in line with current NHS practice. There will be a total of 9 study visits for this group. |
| Low-calorie diet intervention group | Experimental | Dietary Supplement: Low-calorie dietParticipants will received a special diet involving 25 regular visits and intensive management. Participants will be given a supply of especially formulated soups and shakes, a special diet in a form of powder that need to be mixed with 200 ml water. |
Who may qualify
- Ages
- 18 to 55 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (8 listed)
- The investigators shall recruit participants with the following characteristics:
Key exclusion criteria (11 listed)
- Individuals with normal glucose tolerance (NGT) or type 1 or type 2 diabetes (T2D).
- Anyone engaged in active weight loss (>5kg weight loss in the last 6 months), currently engaged with weight management service, previous bariatric surgery, on weight-lowering medications (e.g. orlistat or liraglutide) or with a history of an eating disorder.
- planning pregnancy/6 months post-partum,
- known structural cardiac disease or anyone with major atherosclerotic disease
- history of stroke within the last 3 months
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Standard of careParticipants allocated to the control group will be given standard clinical information regarding healthy eating, physical activity and management of weight, in line with current NHS practise. | Other | Control group |
| Low-calorie dietThe LCD intervention group, will received a well validated, commercially available, intensive weight management protocol Counterweight-Plus. | Dietary supplement | Low-calorie diet intervention group |
Primary outcome
Changes in liver fat >5 percent, determined by MRI, from baseline to after 12 months of intervention.
Time frame: Changes will be measured at baseline and at 12 months.
For liver fat, diagnosis of NAFLD is based on a threshold of a value >5.5 percent. The investigators anticipate having a 45 percent difference in the proportion in whom liver fat percentage reduces by at least 5 percent between the groups (50 percent of LCD will have an absolute reduction in liver fat of 5 percent vs. 5 percent of controls). The investigators chose an absolute reduction of liver fat of 5 percent as this reduction is clinically meaningful.
30 secondary outcomes
Body Mass Index
Time frame: Changes will be measured at baseline and at 12 months.
Body weight
Time frame: Changes will be measured at baseline and at 12 months.
Waist Circumference
Time frame: Changes will be measured at baseline and at 12 months.
Blood pressure
Time frame: Changes will be measured at baseline and at 12 months.
Liver biochemistry: Alanine transaminase
Time frame: Changes will be measured at baseline and at 12 months.
Changes in HbA1c
Time frame: Changes will be measured at baseline, at 12 weeks, at 24 week and at 12 months.
Lipid profile
Time frame: Changes will be measured at baseline and at 12 months.
Metabolic measures of fatty liver
Time frame: Changes will be measured at baseline and at 12 months.
Markers of fibrosis in liver
Time frame: Changes will be measured at baseline and at 12 months.
The NAFLD scoring screening tool
Time frame: Changes will be measured at baseline and at 12 months.
Peripheral insulin sensitivity
Time frame: Changes will be measured at baseline and at 12 months.
Changes in hepatic insulin sensitivity
Time frame: Changes will be measured at baseline and at 12 months.
Changes in insulin secretion
Time frame: Changes will be measured at baseline and at 12 months..
Changes in fatty acid metabolism
Time frame: Changes will be measured at baseline and at 12 months.
Measures of neuropathy: Change in intra-epidermal nerve fibres densities, length and branch densities.
Time frame: Changes will be measured at baseline and at 12 months.
Measures of neuropathy: Change in sural nerve velocity
Time frame: Changes will be measured at baseline and at 12 months.
Measures of neuropathy: Change in sural nerve amplitude
Time frame: Changes will be measured at baseline and at 12 months.
Functional MRI
Time frame: Changes will be measured at baseline and at 12 months.
Appetite measurement
Time frame: Changes will be measured at baseline and at 12 months.
MRI-derived fat volumes
Time frame: Changes will be measured at baseline and at 12 months.
Cardiac structure (volumes)
Time frame: Changes will be measured at baseline and at 12 months.
Cardiac health: cardiac magnetic resonance imaging
Time frame: Changes will be measured at baseline and at 12 months.
Cardiac health: LV Mass Indexed to Body Surface Area
Time frame: Changes will be measured at baseline and at 12 months.
Cardiac health: Multi-parametric cardiac MRI
Time frame: Changes will be measured at baseline and at 12 months.
Changes in early diastolic strain rate by cardiovascular magnetic resonance
Time frame: Changes will be measured at baseline and at 12 months.
Changes in load and contractility of the cardiac function
Time frame: Changes will be measured at baseline and at 12 months.
Charcterisation of organ fat content
Time frame: Changes will be measured at baseline and at 12 months.
Multi-organ MRI measure for pancreas, spleen and kidney
Time frame: Changes will be measured at baseline and at 12 months.
Multi organs pancreas, spleen and kidney volume
Time frame: Changes will be measured at baseline and at 12 months.
Multi organs pancreas, spleen and kidney fat content
Time frame: Changes will be measured at baseline and at 12 months.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 27 Jun 2025.
- Results publication: PubMed 26879684Leslie WS, Ford I, Sattar N, Hollingsworth KG, Adamson A, Sniehotta FF, McCombie L, Brosnahan N, Ross H, Mathers JC, Peters C, Thom G, Barnes A, Kean S, McIlvenna Y, Rodrigues A, Rehackova L, Zhyzhneuskaya S, Taylor R, Lean ME. The Diabetes Remission Clinical Trial (DiRECT): protocol for a cluster randomised trial. BMC Fam Pract. 2016 Feb 16;17:20. doi: 10.1186/s12875-016-0406-2.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Daniel Cuthbertson principal investigator
University of Liverpool
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Low-calorie diet in people with Obesity and NAFLD, run by University of Liverpool at 1 site in United Kingdom.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 8 inclusion and 11 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 27 Jun 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Changes in liver fat >5 percent, determined by MRI, from baseline to after 12 months of intervention. (time frame: Changes will be measured at baseline and at 12 months.). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT04786418, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 27 Jun 2025.