Non Alcoholic Fatty Liver Disease Clinical Trial
— FLIPANOfficial title:
Prevention and Reversion of Non-Alcoholic Fatty Liver Disease in Obese Patients With Metabolic Syndrome by Mediterranean Diet and Physical Activity
Verified date | June 2020 |
Source | University of the Balearic Islands |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This prospective randomized trial evaluates the role of customized dietary and physical
activity intervention on the progression of Non-Alcoholic Fatty Liver Disease (NAFLD) in
patients with obesity and presenting at least three of the main Metabolic Syndrome traits.
The project proposes a personalized nutritional intervention based on a Mediterranean
customized diet which introduces plenty of antioxidant and anti-inflammatory bioactive
components, coupled with physical activity promotion to prevent and reverse NAFLD among obese
patients with metabolic syndrome. This will be compared with two more dietary strategies
including a Mediterranean Diet intervention with seven meals a day and the conventional
dietary approach proposed by the American Association for the Study of Liver Diseases
(AASLD).
Status | Active, not recruiting |
Enrollment | 150 |
Est. completion date | December 1, 2021 |
Est. primary completion date | November 29, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 40 Years to 60 Years |
Eligibility |
Inclusion Criteria: - Age between 40 and 60 years - Diagnosis of NAFLD by ultrasound - BMI = 27 and < 40 kg/m2 - Meeting at least 3 of 5 criteria for the metabolic syndrome [as described in the International Diabetes Federation consensus]: (1) BMI >30kg/m² or increased waist circumference: = 94 cm in males; = 80 cm in females; (2) Triglycerides (TG) levels = 150 mg/dL (1.7 mmol/L) or specific treatment; (3) Reduced HDL cholesterol: < 40 mg/dL (1.03 mmol/L) in males; < 50 mg/dL (1.29 mmol/L) in females or specific treatment; (4) Raised blood pressure: systolic BP = 130 or diastolic BP = 85 mm Hg or treatment of previously diagnosed hypertension; (5) Raised fasting plasma glucose (FPG) = 100 mg/dL (5.6 mmol/L), or previously diagnosed type 2 diabetes - Written informed consent Exclusion Criteria: - Inability or unwillingness to give informed consent or communicate with staff study - Documented history of prior cardiovascular disease [angina; myocardial infarction; coronary revascularization procedures; stroke (ischemic or hemorrhagic including transient ischemic attacks); symptomatic peripheral artery disease that required surgery or was diagnosed with vascular imaging techniques; ventricular arrhythmia; uncontrolled atrial fibrillation; congestive heart failure (New York Heart Association Class III or IV); hypertrophic myocardiopathy; and history of aortic aneurism >=5.5cm in diameter or aortic aneurism surgery] - Documented history of prior liver diseases (other than NAFLD) - Active cancer or a history of malignancy in the last 5 years - Low predicted probability to change food habits according to the Stages of Change Model (Nigg, 1999) - Unwillingness or inability to adhere to the dietary and physical activity intervention over the entire period of the study - Failure to follow scheduled visits - Weight loss (>5 kg) during 6 months prior to visit - Previous surgical procedures for weight loss or scheduled bariatric surgery within the next 12 months - Use of weight loss medications during 6 months prior to visit - Previous history of bowel resection, inflammatory bowel disease - Obesity associated with endocrine disease (except treated hypothyroidism) - Allergy to Mediterranean diet foods or components - Severe psychiatric disorders (schizophrenia, bipolar disorder, eating disorders, or depression with hospitalization within the last 6 months) or Beck Depression Inventory score > 30 - Severe condition with less than 24 months life expectancy - Chronic abuse of drugs or alcohol (>21 and >14 units of alcohol a week for men and women, respectively; 1 unit = 125 mL of wine) - Treatment with steroids - Pregnancy |
Country | Name | City | State |
---|---|---|---|
Spain | University of the Balearic Islands | Palma | Balearic Islands |
Lead Sponsor | Collaborator |
---|---|
University of the Balearic Islands | Fundació La Marató de TV3 |
Spain,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Changes in liver steatosis | The primary outcome is to measure the change of liver steatosis (expressed as percentage of liver steatosis) after applying a different intervention to each group (PA-MD; HMF-MD; or CD) of participants with metabolic syndrome. It will be measured (at baseline, and after 6, 12 and 24 months of intervention) by means of a 1.5-T Magnetic Resonance Imaging (MRI) (Signa Explorer 1.5T, General Electric Healthcare, Chicago, Illinois., U.S.A) by using a 12-channel phased-array coil. |
At baseline, 6, 12 and 24 months | |
Secondary | Changes in liver fibrosis | The secondary otucome is to measure the changes of liver fibrosis (expressed as percentage of liver fibrosis) after applying a different intervention to each group (PA-MD; HMF-MD; or CD) of participants with metabolic syndrome. It will be measured (at baseline, and after 6, 12 and 24 months of intervention) by using Shear Wave Measurement (SWM) (Hitachi Ltd, Japan) and the echograph Arietta V70 (Hitachi Medical System Europe Holding AG, Steinhausen, Switzerland). |
At baseline, 6, 12 and 24 months |
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