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Metabolic Syndrome X clinical trials

View clinical trials related to Metabolic Syndrome X.

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NCT ID: NCT03147339 Completed - Metabolic Syndrome Clinical Trials

The Effects of Restricted Dietary of AGEs on the Glycemic Control, Oxidative Stress and Inflammation

AGEs
Start date: January 10, 2017
Phase: N/A
Study type: Interventional

To evaluate the effects of dietary restriction of advanced glycated end products (AGEs) on glycemic control, oxidative stress and systemic inflammation, in a randomized, 44 subjects with metabolic syndrome for 8 weeks.Both groups will be advised to follow same low energy diet and no changing in physical activity pattern.Parameters related to metabolic syndrome, anthropocentric factors, oxidative stress(Malondialdehyde), CML(AGEs factor in blood) and systemic inflammation factors (hs-CRP وTNF-α ) will be measured at the baseline and at the end of the study.

NCT ID: NCT03142503 Completed - Metabolic Syndrome Clinical Trials

The DIET Trial - Dietetic Intervention in Psoriatic Arthritis

DIET
Start date: January 21, 2013
Phase: N/A
Study type: Interventional

Psoriasis (Ps) and psoriatic arthritis (PsA) are associated with increased risk of metabolic syndrome (MetS), body fatness and cardiovascular risk. Additionally, oxidative stress and inflammation are also contributing mechanisms on Ps and PsA. However, little is known about the influence of diet and micronutrients on the main outcomes of these diseases. The aim of the investigators is to evaluate the effectiveness of an intervention diet program on disease activity, metabolic profile and oxidative stress inpatients with Psoriasis and Psoriatic Arthritis.

NCT ID: NCT03139214 Completed - Metabolic Syndrome Clinical Trials

Parenting Intervention and Metabolic Syndrome

Start date: August 27, 2001
Phase: N/A
Study type: Interventional

This study aimed to test the effect of a parenting intervention on metabolic syndrome in African American youth. The investigators hypothesized that a parenting intervention would produce reductions in metabolic syndrome, particularly for those families that started out high in difficulties with parenting.

NCT ID: NCT03121755 Completed - Obesity Clinical Trials

CCK1R Function in Patient Leukocytes

Start date: January 21, 2015
Phase: N/A
Study type: Observational

The type 1 cholecystokinin receptor (CCK1R) is a potential target for the treatment of obesity, due to the ability of this GI hormone to elicit satiety. However, this receptor has been shown to be sensitive to the cholesterol content of the membrane in which it is expressed. Because some patients who might be candidates for the use of CCK agonists to treat their obesity and co-morbidities, the goal of this study is to determine how metabolic abnormalities might affect the responsiveness of this receptor to CCK. Because the normal site mediating CCK-stimulated satiety is on vagal afferent neurons that cannot easily be studied, we will collect buffy coat cells from a peripheral blood sample from patients involved in the Sangre Por Salud Biobank at Mountain Park Medical Center. Ex vivo, the CCK1R will be expressed on these cells and will be functionally characterized, and the cholesterol content of the cells will be assayed. These data will be correlated with the clinical, biochemical, and metabolic phenotypic data collected as part of the parent study.

NCT ID: NCT03119493 Completed - Metabolic Syndrome Clinical Trials

Periodized Aerobic Interval Training in Metabolic Syndrome

Start date: June 1, 2015
Phase: N/A
Study type: Interventional

Autonomic disfunction present in metabolic syndrome subjects is related by a greater vulnerability of the heart and risk of cardiovascular events. In this context, aerobic interval training has been highlighted by its easy applicability and benefits effects in autonomic modulation in different populations. Therefore the studies that use de aerobic interval training in this different populations didn't realize a periodization of training with preparatory periods with progressive increase of load, specific phases with less duration predominating the intensity and transition periods for recuperation. Additionally, there isn't studies that investigate the effects of aerobic interval training in autonomic modulation of individuals with metabolic syndrome. In this context, periodized aerobic interval training can arise like a new type of treatment that offering security and efficacy in subjects with metabolic syndrome. So, the aim of the study is evaluate the effect of periodized aerobic interval training in cardiac autonomic modulation and cardiovascular and anthropometric parameters of individuals with metabolic syndrome.

NCT ID: NCT03115866 Active, not recruiting - Metabolic Syndrome Clinical Trials

FRUVEDomics: Behavioral Intervention in Young Adults to Identify Metabolomics and Microbiome Risk

FRUVEDomics
Start date: January 15, 2015
Phase: N/A
Study type: Interventional

Rates of obesity and the metabolic syndrome are increasing in the young adult population (years 18-28). Modifying diet, especially increasing fruit and vegetable intake, can help assist in health maintenance and disease prevention. The purpose of this project is to evaluate the impact of the FRUVEDomics behavior intervention on dietary behaviors and metabolic parameters on young adults "at-risk" of disease. FRUVEDomics is an 8-week free-living dietary intervention, based on the USDA Dietary Guidelines for Americans and driven by the Social Cognitive Theory, conducted in young adults (18-28 years old) at West Virginia University. Individuals were recruited if they had pre-existing poor nutritional habits. A metabolic syndrome risk screening score was given to participants at baseline to measure "risk" status for chronic disease. Subjects were randomized into one of three nutritional intervention groups: 1) "FRUVED" (50% fruit & vegetable), 2) "FRUVED+LRC" (50% fruit & vegetable plus low refined carbohydrate), and 3) "FRUVED+LF" (50% fruit & vegetable plus low fat). Anthropometrics, surveys, venous blood samples and body composition were collected before and after the intervention. Group nutrition education including basic nutrition for the prescribed intervention, culinary tool kit distribution, sample budget and grocery shopping tips were delivered to each participant group prior to the start of the intervention. Participants underwent individual weekly consultations with a Registered Dietitian Nutritionist using food logs, food pictures and receipt management, to assess adherence and cost of the intervention.

NCT ID: NCT03111693 Recruiting - Obesity Clinical Trials

CT Evaluation of Cardiovascular Risk Markers in Obese Patients

RisqOScan
Start date: November 2014
Phase: N/A
Study type: Observational

Obesity is a chronic metabolic disorder : it leads to coronary heart disease and early atherosclerosis. Coronary artery calcium measured by CT is known as a robust predictor to predict risk for cardiac events in symptomatic and asymptomatic individuals. Furthermore, recent studies show that other CT risk factor exists, independent of calcium scoring, such as epicardial fat, intrathoracic fat and visceral fat. The aim of this prospective study is to evaluate these new cardiovascular risk markers in obese patients, using standard dose CT and low dose CT with adaptative statistical iterative reconstruction.

NCT ID: NCT03098446 Completed - Metabolic Syndrome Clinical Trials

The Effect of Sitting and Moderate Exercise on Plasma Triglyceride Elevation After a Meal

Start date: April 8, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the effect of 4 days of sitting and moderate exercise on plasma triglyceride elevation after a meal.

NCT ID: NCT03089437 Completed - Metabolic Syndrome Clinical Trials

The Effects of Prolonged Standing Compared to Prolonged Sitting on Postprandial Lipemia

Start date: March 31, 2017
Phase: N/A
Study type: Interventional

The effects of 12 hours of prolonged standing will be compared to prolonged standing on a high fat tolerance test the following day. Plasma triglycerides, insulin, and glucose will be measured in a crossover study design.

NCT ID: NCT03058016 Not yet recruiting - Metabolic Syndrome Clinical Trials

Personalized Nutrition Prediction for Metabolic Syndrome Patients, an Open Single-center Study

Start date: April 1, 2017
Phase: N/A
Study type: Interventional

This clinical study is designed to evaluate the providing of a computational prediction engine for optimization of personalized nutrition Personalized recommendations for effective diet, lifestyle and activities based on the patient's parameters measurements and reactions will be provided on a bi-weekly basis, all Lab tests and dietician control will be performed twice a month.