Calisthenics Versus High Intensity Interval Training in NAFL
Non-Alcoholic Fatty Liver Disease
About this trial
This is an interventional treatment trial for Non-Alcoholic Fatty Liver Disease focused on measuring NAFLD , Calisthenics , High intensity interval training
Eligibility Criteria
Inclusion Criteria: 1. Sixty patients with non-alcoholic fatty liver disease (NAFLD) of both genders. 2. Patients with mild non-alcoholic fatty liver disease (NAFLD) according to ultrasonography fatty liver indicator (US-FLI) score (2-4).( Chen et al.,2020) 3. Their age will be ranged from 30s-40s. 4. Body mass index (BMI) from 30 to 34.9 kg/m2. 5. Body free fat mass (FFM) percentage > 25 % for men,> 35 % for women. 6. Lean body mass (LBM) parentage < 76 % for men; < 69% for women. 7. Waist circumference ≥ 102 cm for men, > 88 cm for women. 8. Waist/Hip ratio > 0.9% for men and > 0.8% for women. 9. Elevated liver enzymes (ALT> 55 U/L, AST> 48 UL, GGT>85 U/L, AST/ALT <1 U/L). 10. Patient with dyslipidemia who has one or more from the following blood lipid values (total cholesterol > 200 mg\dl, LDL > 130 mg\dl, TG >150 mg\dl, HDL< 40mg\dl or LDL/HDL ratio > 4). 11. Low levels of physical activity (using the International Physical Activity Questionnaire- Short Version (IPAQ)) ≤ 10 min walking per day. 12. Liver size estimated by ultrasonography more than 5% from the normal liver size without hepatocellular damage. Exclusion Criteria: The patient will be excluded if he has one of the following:- Unstable cardiovascular problems like arrhythmia and heart failure. Active Hepatitis C virus HCV. Diabetes mellitus (DM). Hypertensive patients (>140/90mmHg). Active Smoker. Chronic chest disease. Patients on medications affecting muscle power as steroids. Auditory and visual problems. Pregnancy & lactation. Clinically significant peripheral vascular disease (ABPI < 80 %). Patients who take beta-blockers. Severe anemia. Patients with chronic renal failure. Musculoskeletal or neurological limitation to physical exercise. Any cognitive impairment that interferes with prescribed exercise procedures. .Participation in regular exercise training of any type in the previous 3 months
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
Experimental
Study group A (Calisthenics exercise)
Study group B (High intensity interval training)
Group (A) (n =30) will receive calisthenics exercise three times /week for eight weeks, patients in this group will receive four forms of calisthenics exercise (squats, curl up, push up, blank) starting free and upgrading intensity according to ability of the patients.
Group (B) (n =30) will receive high intensity interval training three times /week for eight weeks, A motorized treadmill device (KETTLER, laufband alpha run 600, German) with a minimum speed of 0.5km/hr and capability to display the distance in kilometer per hour will be used in this study. Intensity of HIIT will be measured using Bruce protocol to calculate target heart rate of each patient.