In Spain, obesity epidemic is one of the leading contributors of chronic disease and disability. Obesity is associated with higher morbidity and all-cause mortality risk especially when fat is stored in the abdominal area (i.e., increased visceral adipose tissue, VAT). Although current approaches such as energy restriction may be effective at reducing body fat and improving cardiometabolic health, their long-term adherences are limited. Time-restricted eating (TRE; e.g., 8 hours eating: 16 hours fasting on a daily basis) is a recently emerged intermittent fasting approach with promising cardiovascular benefits. Results from pioneering pilot studies in humans are promising and suggest that simply reducing the eating time window from ≥12 to ≤8-10 hours/day improves cardiometabolic health. However, currently, there is no consensus regarding whether the TRE eating window should be aligned to the early or middle to late part of the day. The EXTREME study will investigate the efficacy and feasibility of three different 8 hours TRE schedules (i.e., early, late and self-selected) over 12 weeks on VAT (main outcome) and cardiometabolic risk factors (secondary outcomes) in adults with overweight/obesity and abdominal obesity. The final goal of the EXTREME study is to demonstrate the health benefits of a novel and pragmatic intervention for the treatment of obesity and related cardiometabolic risk factors; an approach readily adaptable to real-world practice settings, easy for clinicians to deliver, and intuitive for patients to implement and maintain in their lives.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
197
Participants will eat ad libitum within an 8-hour early eating window starting not later than 10am. No calorie-containing food or beverage intake will be allowed outside the 8-hour eating window. Participants will also receive standard recommendations on healthy lifestyle based on Mediterranean dietary pattern and physical activity recommendations for weight loss and health promotion
Participants will eat ad libitum within an 8-hour late eating window starting not earlier than 1pm. No calorie-containing food or beverage intake will be allowed outside the 8-hour eating window. Participants will also receive standard recommendations on healthy lifestyle based on Mediterranean dietary pattern and physical activity recommendations for weight loss and health promotion
Participants will self-selected an 8-hour eating window to eat ad libitum. No calorie-containing food or beverage intake will be allowed outside the 8-hour eating window. Participants will also receive standard recommendations on healthy lifestyle based on Mediterranean dietary pattern and physical activity recommendations for weight loss and health promotion
Universidad Pública de Navarra
Pamplona, Navarre, Spain
University of Granada
Granada, Spain
Change in visceral adipose tissue
Visceral adipose tissue will be assessed by Magnetic Resonance Imaging (MRI)
Time frame: Change from baseline to 12 weeks
Change in Hepatic fat content
Hepatic fat content will be assessed by Magnetic Resonance Imaging (MRI)
Time frame: Change from baseline to 12 weeks
Change in Pancreatic fat content
Pancreatic fat content will be assessed by Magnetic Resonance Imaging (MRI)
Time frame: Change from baseline to 12 weeks
Change in Intramuscular fat content
Intramuscular fat content will be assessed by Magnetic Resonance Imaging (MRI)
Time frame: Change from baseline to 12 weeks
Change in Hepatic elasticity
Hepatic elasticity will be assessed by US elastography
Time frame: Change from baseline to 12 weeks
Change in Pancreatic elasticity
Pancreatic elasticity will be assessed by US elastography
Time frame: Change from baseline to 12 weeks
Change in Fasting glucose metabolism
Fasting blood samples will be used to analyse different biomarkers of glucose metabolism
Time frame: Change from baseline to 12 weeks
Change in Fasting lipid metabolism
Fasting blood samples will be used to analyse different biomarkers of lipid metabolism (e.g., triglycerides, total cholesterol, high-density lipoprotein cholesterol, low-density lipoprotein cholesterol)
Time frame: Change from baseline to 12 weeks
Change in Inflammatory profile
Fasting blood samples will be used to analyse inflammatory profile (e.g., C-reactive protein and interleukin 6)
Time frame: Change from baseline to 12 weeks
Change in Hepatic profile
Fasting blood samples will be used to analyse hepatic profile (e.g., alkaline phosphatase, bilirubin, alanine transaminase and gamma-glutamyl transferase)
Time frame: Change from baseline to 12 weeks
Change in Kidney profile
Fasting blood samples will be used to analyse kidney profile (e.g., creatinine and creatine kinase)
Time frame: Change from baseline to 12 weeks
Change in Glycemia (Continuous Glucose Monitoring)
Glycemia will be assessed by Continuous Glucose Monitoring during 2 weeks
Time frame: Change from baseline to 12 weeks
Change in Body weight
Body weight will be measured by a digital scale
Time frame: Change from baseline to 12 weeks
Change in Body composition (Fat mass and fat free mass)
Body composition will be assessed by Dual-energy X-ray Absorptiometry (DXA)
Time frame: Change from baseline to 12 weeks
Change in Anthropometric measures
Neck, hip and waist circumferences will be assessed by standard procedures
Time frame: Change from baseline to 12 weeks
Change in Blood pressure
Systolic and Diastolic blood pressure will be assessed by standard procedures
Time frame: Change from baseline to 12 weeks
Change in energy intake
Energy intake (kcal/day) will be assessed by 24h recalls
Time frame: Change from baseline to 12 weeks
Change in macronutrients intake
Macronutrients intake (g/day and percentage of energy intake) will be assessed by 24h recalls
Time frame: Change from baseline to 12 weeks
Change in dietary habits
Dietary habits will be assessed by food frequency questionnaires
Time frame: Change from baseline to 12 weeks
Change in Food craving
Food craving will be assessed by the Food Craving Inventory (FCI)
Time frame: Change from baseline to 12 weeks
Change in Appetitive traits
Appetitive traits will be assessed by the Adult Eating Behavior Questionnaire (AEBQ)
Time frame: Change from baseline to 12 weeks
Change in Subjective sleep quality
Subjective sleep quality will be assessed by the Pittsburgh Sleep Quality Index (PSQI)
Time frame: Change from baseline to 12 weeks
Change in Objectively sleep quality
Objectively sleep quality will be assessed by accelerometry
Time frame: Change from baseline to 12 weeks
Change in Chronotype
Chronotype will be assessed by the Munich Chronotype Questionnaire (MCTQ)
Time frame: Change from baseline to 12 weeks
Change in Morning-Evening type
Morning-Evening type will be assessed by the Morningness-Eveningness Questionnaire Self-Assessment Version.
Time frame: Change from baseline to 12 weeks
Change Subjective physical activity levels
Subjective physical activity levels will be assessed by the International Physical Activity Questionnaire short form
Time frame: Change from baseline to 12 weeks
Change Objectively physical activity levels
Objectively physical activity levels will be assessed by accelerometry
Time frame: Change from baseline to 12 weeks
Change in Depression aspects
Depression aspects will be assessed by the Beck Depression Inventory Fast Screen (BDI-FS)
Time frame: Change from baseline to 12 weeks
Change in Stress aspects
Stress aspects will be assessed by the Perceived Stress Scale (PSS)
Time frame: Change from baseline to 12 weeks
Change in Anxiety aspects
Anxiety aspects will be assessed by the State-Trait Anxiety Inventory (STAI)
Time frame: Change from baseline to 12 weeks
Change in General health
General health will be assessed by the EuroQol 5 dimensions 5 levels (EQ-5D-5L)
Time frame: Change from baseline to 12 weeks
Change in Quality of life
Quality of life will be assessed by the Rand Short Form 36 (SF-36)
Time frame: Change from baseline to 12 weeks
Change in Gut microbiota composition
DNA sequencing to determine gut microbiota composition (e.g., phylum and genera)
Time frame: Change from baseline to 12 weeks
Change in Gut microbiota diversity
DNA sequencing to determine gut microbiota diversity (e.g., beta and alpha)
Time frame: Change from baseline to 12 weeks
Feasibility of recruitment
Feasibility of recruitment (i.e., percent of response rate).
Time frame: 12 weeks
Feasibility of the intervention
Retention during the intervention (i.e., percent of attrition).
Time frame: 12 weeks
Adherence to the intervention
Adherence will be assessed by eating records
Time frame: Every day during the intervention, up to 90 days
Genetic variants in Clock genes
Genetic variantes in clock genes will be determined by Illumina sytem
Time frame: Baseline
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