Obesity Clinical Trial
Official title:
Evaluation of Liver and Cardiometabolic Health Benefits on Low Carbohydrate Ketogenic Diet
To evaluate the impact of a Low Carbohydrate Ketogenic Diet (LCKD) weight loss program and compare to the standard of care program established for patients with Non-Alcoholic Fatty Liver Disease (NAFLD) on: (1) Liver fat and liver stiffness scores, (2) lipid profile and insulin sensitivity; and (3) depression scores and quality of life, and (4) Cardiometabolic measures such as cardiopulmonary exercise test (CPET) and transthoracic echocardiogram (TTE).
This prospective pilot pragmatic trial will investigate the role of a LCKD weight loss
program for obese patients (BMI ≥30 kg/m2) and compare it to the group of known obese NAFLD
patients who receive dietetic counseling as part of their standard of care in a dedicated
NAFLD program. All participants (n=50) will be recruited at Virginia Commonwealth University
(VCU).
Patients will do initial paperwork including
Questionnaires QOL, eating disorder screen, depression screen:
QOL, eating disorder screen and depression screen.
Labwork:
Data will be collected from routine care labwork to include a fasting cholesterol panel,
insulin, A1c and comprehensive panel (if they have not received these labs in the preceding 3
months), and at 6 and 12 months. A1c will be collected at 3,6,9 months as well (if A1c >/=7),
or just additionally at 6 months if A1c <7
Study labs will be collected:
Blood at 0, 3, 6 and 12 months Urine, stool and saliva at 0, 1, 3 and 12 months
Fibroscan will be done at 0, 3, 6 and 12 months
Echo/CPET testing and Room calorimetry will be offered and the patients agreeing to do this
will have them done at 0, 3 and 12 months
;
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