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Prediabetic State clinical trials

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NCT ID: NCT03193229 Completed - Obesity Clinical Trials

MapTrek to Increase Activity Among Patients at Risk for Type 2 Diabetes

Start date: May 15, 2017
Phase: N/A
Study type: Interventional

The overarching objective of our work is to provide an inexpensive and scalable m-health tool to increase both volume and intensity of physical activity and reduce sedentary behavior in patients at risk for type 2 diabetes. The objective of this study is to pilot test MapTrek, a text-messaging based intervention.

NCT ID: NCT03184337 Completed - Metabolic Syndrome Clinical Trials

Women's Lifestyle Balance Study

LB
Start date: April 24, 2017
Phase: N/A
Study type: Interventional

This pilot study aims to determine whether adding a sleep extension and sleep hygiene intervention to an existing lifestyle improvement program improves its efficacy for weight loss in those at risk for diabetes and cardiovascular disease. Half of the participants will receive the Centers for Disease Control's standard PreventT2 program and half of the participants will receive the same program with an additional sleep intervention.

NCT ID: NCT03178019 Completed - Overweight Clinical Trials

DPP4 Activity, Microvascular Reactivity and Inflammation

DPP4
Start date: February 1, 2014
Phase: N/A
Study type: Observational

Dipeptidyl peptidase 4 (DPP4) is a serine exopeptidase able to inactivate various oligopeptides involved in inflammation, immunity and vascular function. Our aim was to investigate the associations between constitutive levels of DPP4 activity and inflammatory biomarkers, skin microvascular reactivity, gut peptides, insulin resistance indexes, heart rate and blood pressure variability, and measures of adiposity in subjects with different grades of glucose tolerance.

NCT ID: NCT03167996 Completed - Hypertension Clinical Trials

Chronic Cardiovascular Risk Outpatient Management in South Asians Using Digital Health Technology

HealthPals
Start date: June 23, 2016
Phase: N/A
Study type: Interventional

This platform will enable investigation the cardiovascular risk reduction and the increase in participant engagement in their heart-healthy goals, through the use of virtual care/telemedicine with a digital platform that connects them to their own doctors, nurses, and dietitians.

NCT ID: NCT03154073 Completed - Aging Clinical Trials

Effects of Progressive Intensity Exercise Training on Glycemic Control in Older Adults

GLYDE
Start date: July 20, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the effects of moderate versus vigorous intensity exercise training on glycemic control in older adults. Glycemic control will be assessed using an oral glucose tolerance test and continuous glucose monitors. In addition, the investigaotrs will investigate whether engaging in an exercise training program elicits changes in sedentary behavior, non-exercise physical activity, sleep, and total daily energy expenditure.

NCT ID: NCT03136289 Completed - Adolescent Behavior Clinical Trials

Family Consumer Behaviors, Adolescent Prediabetes and Diabetes

Start date: December 2013
Phase: N/A
Study type: Observational

The aim of this study was to examine the association between family consumer behaviors (healthy food availability and supermarket spending) and adolescent prediabetes and diabetes.

NCT ID: NCT03126981 Completed - PreDiabetes Clinical Trials

Effects of Almonds on Insulin Sensitivity in Prediabetes

Start date: April 20, 2017
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to evaluate the effects of consuming 1.5 oz almonds twice daily on insulin sensitivity and markers of cardiometabolic health in men and women with prediabetes.

NCT ID: NCT03124134 Completed - Obesity Clinical Trials

Gelesis Glycemic Index Study

GLIDE
Start date: April 18, 2017
Phase: N/A
Study type: Interventional

A study to determine glucose and insulin responses to 50g and 100 g of carbohydrate with and without Gelesis200.

NCT ID: NCT03117829 Completed - PreDiabetes Clinical Trials

Study: Diet and Exercise Study to Improve Brain Blood Flow: Blood Flow Improvement Trial

BFIT
Start date: March 15, 2017
Phase: N/A
Study type: Interventional

Project Summary Metabolic syndrome (MetS) is associated with the development of diabetes and cardiovascular disease; however it is also linked with cognitive decline and dementia. The study investigators have shown that MetS is associated with lower cerebral blood flow (CBF) and memory function in late middle-aged adults at increased risk for developing Alzheimer's disease (AD). Insulin resistance (IR) is at the core of MetS, and a hallmark feature of IR is higher fasting blood glucose (FBG) as well as post prandial hyperglycemia. While the study investigators and others have demonstrated links between IR and CBF as well as cognition from an observational perspective, no studies have investigated CBF and cognition after an intervention involving exercise and a carbohydrate restricted diet (CRD) designed to improve or normalize IR and glucose homeostasis. The study investigators propose to determine the effect of improving or normalizing glucose homeostasis on CBF and cognition, through diet and exercise, in individuals with IR and at risk for the development of AD. While exercise and a CRD have been shown to improve IR and glycemic control, we have only limited knowledge of the mechanisms behind these improvements. Nutritional metabolomics, the global measurement and interpretation of metabolic profiles, assesses the interaction of diet with the endogenous gene-protein cascade and the gut microbiome. Additionally, exercise has been shown to have an impact on the human metabolome. Finally, numerous metabolites have been specifically linked to IR and impaired fasting glucose (IFG). The study investigators propose to use metabolomics to measure changes in metabolites as individuals normalize or improve IR and glucose homeostasis. Should this exploratory study reveal increased brain blood flow and improved memory in response to diet and exercise, then early treatment of these individuals at risk might offer new avenues for disease-course modification. Strategies towards early and effective risk factor management could be of value in reducing the risk of metabolic as well as cognitive decline. In addition, should this study reveal changes in metabolic abnormalities consistent with early indications of diabetes, metabolomics could be an effective approach to complement disease risk analysis in our goal toward precision care.

NCT ID: NCT03113916 Completed - Obesity Clinical Trials

De Por Vida: A Diabetes Risk Reduction Intervention for Hispanic Women

Start date: June 23, 2014
Phase: N/A
Study type: Interventional

This pragmatic randomized clinical trial will assess the efficacy, cost, and sustainability of a culturally tailored weight-loss program targeting obese Hispanic women with pre-diabetes or T2D. The intervention will be integrated into patient care at a Federally Qualified Health Center serving over 30,000 low-income patients, and will be delivered by trained clinic staff, with minimal support from research staff. After the effectiveness clinical trial, two cohorts of clinic patients will receive the intervention in a sustainability test.