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Body Weight clinical trials

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NCT ID: NCT02923674 Completed - Obesity Clinical Trials

Empowered With Movement to Prevent Obesity and Weight Regain

EMPOWER
Start date: December 6, 2016
Phase: N/A
Study type: Interventional

This study will help determine the appropriate type, amount and intensity of physical activity most beneficial for preventing weight regain after weight loss in older adults.

NCT ID: NCT02911337 Completed - Weight Loss Clinical Trials

Weight Loss as Therapy for Heart Failure With Preserved Ejection Fraction

WTLSSCHF
Start date: August 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to examine the efficacy of an intensive, supervised, lifestyle modification program on symptoms and signs of heart failure as well as laboratory and echocardiographic measures of cardiac structure and function. This will be a 6 month trial in 50 patients with a clinical diagnosis of heart failure with preserved ejection fraction (HFpEF). Patients will be enrolled in the Medical University of South Carolina weight management 15 week lifestyle change program which will involve weekly visits that rotate among the clinical specialities (dietary, exercise and behavioral) and scheduled visits with the research Registered Nurse. Each patients baseline data will be used as the control and compared with the same measurements at the 6 month end point.

NCT ID: NCT02906787 Completed - Smoking Cessation Clinical Trials

Behavioral Activation for Smoking Cessation and the Prevention of Post-Cessation Weight Gain

Start date: September 13, 2016
Phase: N/A
Study type: Interventional

The purpose of this research study is to better understand (1) why people gain weight when they quit smoking and (2) whether certain types of smoking cessation (i.e. quit smoking) counseling combined with the nicotine patch help people quit smoking and gain less weight.

NCT ID: NCT02899559 Completed - Body Weight Clinical Trials

Messages and Plans to Increase Gym Utilization

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

This primary object of this study is to test to the hypothesis that the both the nudge and boost messages will increase short term gym utilization relative to the control condition but that only the boost message will increase long-term gym utilization. Non-technical summary: College students will receive one of three messages about exercise. Their card swipe data as a measure of gym utilization will be tracked as an assessment of the effect of those messages.

NCT ID: NCT02896140 Completed - Obesity Clinical Trials

Effect of Dairy Consumption on Glycemic Control, Body Weight and Cardiovascular Risk Factors

Start date: April 2016
Phase:
Study type: Observational

The aim of this study is to determine the relationship between the percentage of calories from dairy intake and long-term glycemic control and weight maintenance in patients with type 2 diabetes who participate in an intensive lifestyle intervention program. The investigators hypothesize that overweight and obese patients with type 2 diabetes who consume higher percentage of calories from dairy products during intensive lifestyle intervention programs have better glycemic control and maintenance of weight loss as compared to those who consume lower percentage of calories from dairy products.

NCT ID: NCT02895867 Completed - Type 2 Diabetes Clinical Trials

Effect of Dairy Consumption on Glycemic Control, Body Weight and Cardiovascular Risk in Patients With Type 2 Diabetes

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

This is a randomized prospective clinical study in patients with type 2 diabetes to evaluate the effect of dairy products with full or low fat on glycemic control and cardio-metabolic risk factors in comparison to a regular diet.

NCT ID: NCT02893319 Completed - Body Weight Clinical Trials

Maternal and Infant Growth Study

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

Rapid growth early in infancy is a risk factor for obesity and cardiovascular disease later in the lifespan. Evidence is limited, but both pre- and postnatal factors are associated with early rapid growth, and include high maternal BMI prior to pregnancy and excessive gestational weight gain. This research focuses on aspects of early feeding as potentially modifiable factor affecting early infant weight gain. Formula feeding mothers are randomized to receive either 5 oz of 8 oz bottles to use in feeding their infants from 2- to 16 weeks postpartum. In addition, a reference group of exclusively breastfeeding mother-infant dyads are also included. The hypothesis is that differences in feeding practices will be associated with differences in growth and that infants randomized to be fed from smaller bottles will grow more slowly that those randomized to larger bottles. Growth patterns of formula fed infants will also be compared to those of exclusively breastfed infants.

NCT ID: NCT02877004 Completed - Weight Loss Clinical Trials

LLLT for Reducing Waste Circumference and Weight

LLLT
Start date: September 30, 2016
Phase: N/A
Study type: Interventional

The purpose of this research is to gather preliminary information on the effectiveness of Low Level Laser Therapy (LLLT) in helping people reduce their weight gain in the central body region.

NCT ID: NCT02840916 Completed - Clinical trials for Postpartum Weight Retention

Laser Acupuncture for Postpartum Weight Retention

Start date: January 2014
Phase: Phase 3
Study type: Interventional

Objective: To determine the therapeutic effect of acupuncture on postpartum weight retention. Methods: 66 subjects after delivery with postpartum weight retention will be randomly divided into laser acupuncture and control group. A single-blind clinical trial will be conducted and the subjects will be treated with verum or sham laser acupuncture 5 sessions per week. After about 3 weeks of treatment, the differences of the subjects' body weight, body mass index, and waist circumference will be analyzed with ANOVA between laser acupuncture and control group.

NCT ID: NCT02812264 Completed - Weight Loss Clinical Trials

Using an API to Commercialize an Evidence-Based Weight Loss Intervention

Start date: June 7, 2017
Phase: N/A
Study type: Interventional

This study will test the effectiveness of a mobile application that uses an Application Program Interface (API) to distribute evidence-based weight loss interventions. Half of the participants will receive this API-based application, and the other half of the participants will use a non API-based application.