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Weight clinical trials

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NCT ID: NCT02005224 Completed - Insulin Sensitivity Clinical Trials

Effect of Low-carbohydrate/High-fat Diet on Glucose Tolerance and Lipid Profile in Lean, Healthy Women

LCHF
Start date: August 2012
Phase: N/A
Study type: Interventional

Intervention studying the effect of a low-carbohydrate/high-fat (LCHF) diet as well as on bout of exercise in combination with either a normal diet or a LCHF diet, in relation to glucose metabolism, insulin sensitivity, lipid profile and body composition.

NCT ID: NCT01770366 Completed - Physical Activity Clinical Trials

A Virtual Support Pilot Program for Weight Loss Surgery Patients

Start date: January 2013
Phase: Phase 1/Phase 2
Study type: Interventional

Obesity affects over one-third of the US population, and is associated with serious medical problems like diabetes and heart disease. Weight loss surgery is the most effective treatment for obesity, but some weight loss surgery patients lose less weight than others, and some patients regain the weight they lost. Researchers have found that support groups help post-surgical patients lose more weight, but long-term support programs often aren't available or are difficult for patients to get to. Physical activity is also important for weight loss surgery patients, but most post-surgical support programs don't focus on helping patients exercise. Our pilot study will test an Internet-based weight loss surgery support program that patients can use from home, and will include new devices such as wireless weight scales and wireless pedometers to help patients track their weight loss and physical activity and share their progress with their clinicians over the Internet. If successful, our support intervention will help more patients successfully lose weight after surgery, and therefore will improve their long-term health.

NCT ID: NCT01763775 Completed - Body Fat Disorder Clinical Trials

Clinical Trial of Transtek Body Fat Analyzer (GBF-1251-B & Other 3 Models)

BS-BT
Start date: October 2012
Phase: N/A
Study type: Interventional

The clinical protocol of the clinical testing of this device: 1. Objective of the test: To verify the functions and efficiency of devices. 2. Test methods and procedures: Comparison Test. 3. Device Under Test (DUT): Transtek Body Fat Analyzer, Model: GBF-1251-B, BF-1255-B, BF-1256-B, and GBF-1257-B. 4. Comparison device: Transtek, Glass Body Fat Analyzer, GBF-950-D. 5. Study endpoints: DUT and the comparison device are substantial equivalence. 6. Statistical methodology used: Description of statistical methods.

NCT ID: NCT01507090 Completed - Weight Clinical Trials

Validation of the Mercy TAPE

TAPE
Start date: February 2012
Phase: N/A
Study type: Observational

In 'real-world' health care settings there exist a number of circumstances where the weight of a child is desirable or even necessary but unavailable. Numerous weight estimation strategies have been described but each has limitations. Investigators at Children's Mercy Hospitals and Clinics recently developed a weight estimation method and tool that addresses the limitations of previously published methods. This study is intended to validate the device in a population of children 2 months to 16 years of age.

NCT ID: NCT01501994 Completed - Weight Clinical Trials

Personalized Approach for Promoting Physical Activity in Mayo Clinic Physicians

Start date: July 2009
Phase: N/A
Study type: Interventional

The purpose of the study is to determine if providing physicians with a walking workstation, exercise counseling, and accelerometer feedback about activity will increase physician activity.

NCT ID: NCT01440894 Completed - Body Fat Disorder Clinical Trials

Clinical Trail of Transtek Glass Body Fat Analyzer

GBFA
Start date: February 2011
Phase: N/A
Study type: Observational

The clinical protocol of the clinical testing of this device: 1. Objective of the test: To verify the functions and efficiency of devices. 2. Test methods and procedures: Comparison Test. 3. DUT(Device Under Test): Transtek Glass Body Fat Analyzer, Model: GBF-733-W1, GBF-1012, BF-1039, BF-1041-A, and GBF-950-D. 4. Comparison device: Transtek Glass Body Analyzer, GBF-950 (Predicate Device). 5. Study endpoints: Transtek devices and the predicate device are substantial equivalence. 6. Statistical methodology used: Description of statistical methods. 7. Result: Efficiencies of Transtek devices and predicate device are in the same level.

NCT ID: NCT01342471 Completed - Physical Activity Clinical Trials

Physical Activity and Leisure-time Study (PALS)

PALS
Start date: September 2010
Phase: Phase 1
Study type: Interventional

Physical inactivity is a major public health problem and a primary contributing factor to the obesity epidemic. While most Americans do not meet the physical activity (PA) guidelines (30 min/day, 5 day/wk), they do report watching several hours of TV each day, and frequently site "lack of time" as a barrier for engaging in PA. The Physical Activity and Leisure-time Study examines an approach convert sedentary TV watching into active TV watching time by having adults step in place during commercials (TV commercial stepping).

NCT ID: NCT01296048 Completed - Body Fat Disorder Clinical Trials

Clinical Test for Transtek Glass Body Analyzer

GBA
Start date: November 2010
Phase: N/A
Study type: Observational

The clinical protocol of the clinical testing of this device: 1. Objective of the test: To verify the functions and efficiency of devices. 2. Test methods and procedures: Comparison Test. 3. DUT: Transtek Glass Body Analyzer, Model: GBF-830, GBF-835, GBF-950, and SA-15. 4. Comparison device: Scaleman Body Fat Scales, FS-148BW1 (Predicate Device). 5. Study endpoints: Transtek devices and the predicate device are substantial equivalence. 6. Statistical methodology used: Description of statistical methods. 7. Result: Efficiencies of Transtek devices and predicate device are in the same level.

NCT ID: NCT01253876 Completed - Weight Clinical Trials

Effect of Soymilk Replacement on Anthropometric and Blood Pressure Value

Start date: March 2010
Phase: Phase 4
Study type: Interventional

Soymilk components such as isoflavones, essential fatty acids, phytoesterols, good fats, inositols might have beneficial effects on weight control and blood pressure management. Most studies in this regard have been conducted on postmenopausal or premenopausal women and there are few studies on female youths. Therefore, we are going to determine the effects of soy consumption on the weight, waist circumference and blood pressure in overweight and obese female youths. This was a cross-over randomized clinical trial which was conducted in 2010 in Isfahan on overweight or obese young female youths. After three weeks run-in, females were randomly assigned to consume a diet containing caw's milk or a diet in which only one glass of soy milk was substituted; each one for six weeks. Random sequencing generated in SPSS was used for allocating females in different group randomly. Patients were not blinded because they had to use soy milk in one period of trial and use caw's milk in another period.

NCT ID: NCT01180465 Completed - Weight Clinical Trials

A Dose-ranging, Study of the Safety and Efficacy of Subcutaneous Injections of LIPO-102 Compared With Placebo for the Reduction of Abdominal Subcutaneous Adiposity

Start date: April 2010
Phase: Phase 2
Study type: Interventional

LIPO-102 is under evaluation for treatment of abdominal adiposity