Obesity Clinical Trial
Official title:
Effects of Low-intensity Resistance Exercise Training and Diet on Central Hemodynamics and Arterial Stiffness in Obese Middle-aged Women With High Blood Pressure
- Obesity is a major risk factor for premature arterial abnormalities including high
blood pressure and increased stiffness. Previous studies have shown that weight loss
via lifestyle modifications is associated with a decrease in large artery (aorta)
stiffness. However, along with decreases in fat mass, hypocaloric diet reduces muscle
mass. Low-intensity resistance exercise training (LIRET) results in similar increases
in muscle mass and strength than those observed after high-intensity resistance
exercise.
- The investigators hypothesis is that weight loss via diet combined with LIRET would
additively reduce arterial stiffness and blood pressure (BP) in obese women. The
investigators also hypothesize that the improved arterial function with weight loss
would be associated with beneficial changes in the main mechanisms involved in BP
regulation.
The purpose of the study is to examine the effects of 12 weeks of low-intensity resistance
exercise training (LIRET) and diet on arterial function, autonomic function, and body
composition in obese women with high blood pressure (BP). Specific aims of the study are to:
- To evaluate the extent to which diet and LIRET will improve body composition assessed
by changes in fat mass and lean mass using dual-energy x-ray absorptiometry and waist
circumference.
- To investigate that combined diet and LIRET are more efficacious than either treatment
alone in ameliorating cardiovascular disease risk factors by assessing arterial
stiffness (aortic, systemic, and leg), aortic BP and wave reflection, and autonomic
function (heart rate variability, vascular sympathetic activity [low-frequency power of
systolic BP variability], and baroreflex sensitivity). Circulating levels of
adipocytokines (adiponectin and leptin) and endothelial-derived vasodilators (NO
metabolites [NOx] and prostacyclin) and vasoconstrictors (endothelin-1 and
prostaglandin F2α) will be assessed as secondary outcome variables.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Basic Science
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