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Prediabetic State clinical trials

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NCT ID: NCT02621008 Recruiting - Hypertension Clinical Trials

Mobile Phone-based Intervention for Promoting Healthy Habits and Weight Loss

Start date: November 2015
Phase: N/A
Study type: Interventional

A self administered 16 weeks plus follow up study to explore the efficacy of mobile phone driven apps for stress reduction coupled with guidance for healthy living among obese and overweight populations. The Study primary end points are weight of the participants, as well as glucose measurements (for subject with diabetes) and blood pressure (of subjects with hypertension).

NCT ID: NCT02617693 Completed - Clinical trials for Diabetes Mellitus, Type 2

Development of Pre-pregnancy Intervention to Reduce the Risk of Diabetes and Prediabetes

Jom Mama
Start date: November 23, 2015
Phase: Phase 4
Study type: Interventional

This study is conducted in Asia. The aim of this study is to assess the efficacy of a pre-pregnancy life style intervention to reduce the risk of diabetes and prediabetes.

NCT ID: NCT02609243 Recruiting - Obesity Clinical Trials

Diabetes Nutrition Algorithm - Prediabetes

DiNA-P
Start date: July 2013
Phase: N/A
Study type: Interventional

Prediabetes, defined by either impaired fasting glucose and/or impaired glucose tolerance, is a known high-risk condition predisposing to future diabetes mellitus type 2. Strategies to prevent progression from prediabetes to diabetes have been widely studied, however, without striking long-term effects of any kind of intervention (pharmacological, behavioral...). The investigators therefore investigate certain nutritional approaches concerning nutrient content and favorable food components, targeting metabolic improvement.

NCT ID: NCT02605148 Active, not recruiting - Type 1 Diabetes Clinical Trials

TEFA Family Prevention: Glutenfree Diet to Preserve Beta-cell Function

TEFA
Start date: December 2015
Phase: N/A
Study type: Interventional

To evaluate the effect of Gluten Free Diet (GFD) on beta-cell function and glucose metabolism in subjects with one or several islet autoantibodies without and with dysglycemia at baseline. Additionally, all subjects will be given treatment with Vitamin D, omega fatty acids and probiotics. Subjects will be randomized to GFD or normal diet during 18 months. Beta cell function will be evaluated at baseline, and during follow-up by glucose tolerance tests.

NCT ID: NCT02596776 Completed - Metabolic Syndrome Clinical Trials

Cold Induced Changes in White Adipose

Start date: March 2016
Phase: Early Phase 1
Study type: Interventional

An adaptation to a cold environment is a tendency to generate heat within our body. Some of this heat comes from our fat tissue. Although most fat tissue is "white fat", there are pockets deep within the body that are called "brown fat", which are specially adapted to burning fat and making heat. The investigator believes that our white fat, just underneath the surface of our skin, also has this property to burn fat and make heat, although not at the high level of brown fat. This study is to examine this fat-burning property of the white fat under the skin in response to seasons and to cold. Many such studies have been done in mice, but little has been done in humans. There are a number of factors, including age, weight, and medical history, that may make a person eligible or ineligible to participate in this study. Certain medications could make a person ineligible, but if these medications can be safely altered, the individual may become eligible.

NCT ID: NCT02583061 Recruiting - Clinical trials for Type 2 Diabetes, Gestational Diabetes, Pre-diabetes

Toronto Gestational Glucose Tolerance Cohort

Start date: September 2003
Phase:
Study type: Observational

In this prospective observational cohort study, women representing the full spectrum of gestational glucose tolerance status are undergoing longitudinal cardiometabolic characterization at regular intervals in the years after the index pregnancy.

NCT ID: NCT02565979 Completed - Pre-diabetes Clinical Trials

Long-term Resveratrol and Metabolism

Start date: April 2016
Phase: N/A
Study type: Interventional

The main objective of the study is to investigate if 6 months resveratrol supplementation can improve glucose tolerance in overweight/obese individuals. As secondary objectives we want to investigate whether resting energy metabolism, intra-hepatic lipid content, physical performance, body composition and quality of life change by 6 months resveratrol supplementation in these individuals.

NCT ID: NCT02561377 Recruiting - Prediabetic State Clinical Trials

Effect of Resistance Training on Metabolic Control and Outcome in Prediabetes (NMR-based Metabonomics)

Start date: September 2015
Phase: N/A
Study type: Interventional

This study evaluates the efficacy of a 12-month resistance training on metabolic control and reducing the risk of diabetes.

NCT ID: NCT02559479 Recruiting - Obesity Clinical Trials

A Study to Assess the Effect of a Normal vs. High Protein Diets in Carbohydrates Metabolism in Obese Subjects With Diabetes or Prediabetes

Start date: September 2015
Phase: N/A
Study type: Interventional

The objective of the study is to assess the effect of low-calorie diets with normal (18%) vs. high (35%) protein (mainly coming from animal source) composition on body weight and carbohydrates metabolism in overweight and obese subjects with pre-diabetes or diabetes. A dietary intervention is carried out during 6 months in 100 subjects who are individually randomized to an energy-restricted diet with two types of macronutrients composition: 1) 35% protein, 30% fat and 35% carbohydrates and 2) 18% protein, 30% fat and 52% carbohydrates. Around 80% of total protein in diet comes from animal source (of whom around 40% from lean red meat). Subjects are provided with weekly menus and different recipes to use them as part of the diet. Monitoring visits with the nutritionist will be performed every 15 days. At the beginning of the study, after 3 and 6 months, the following parameters are determined: anthropometric (weight, waist circumference, body mass index and body composition), blood pressure, dietary (72-hours dietary registry) and exercise and biochemical analysis (total cholesterol, triglycerides, HDL cholesterol, LDL cholesterol, apolipoproteins A1 and B, iron, transferring, ferritin, uric acid, glucose, HbA1c, insulin, adiponectin and resistin). Urine samples are also collected to assess microalbuminuria and ureic nitrogen.

NCT ID: NCT02552355 Completed - Physical Activity Clinical Trials

Milk Protein Feeding After Aerobic Exercise in Older Adults With Pre-diabetes Taking the Biguanide Metformin

Start date: August 2015
Phase: Phase 2
Study type: Interventional

The investigators propose that post-exercise milk protein feeding will enhance the mitochondrial protein synthesis (biogenesis) response to an exercise-training program. In addition, the investigators propose that this stimulatory effect of protein feeding will overcome the potential blunting effect of metformin on exercise responses. The investigators will investigate these outcomes over a 12-week exercise-training program in older adults with pre-diabetes with or without metformin treatment.