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Body Weight clinical trials

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NCT ID: NCT02416921 Completed - Obesity Clinical Trials

Preventing Weight Gain in African American Reproductive-Aged Women

FB--Pilot
Start date: April 2015
Phase: N/A
Study type: Interventional

The purpose of this research study is to evaluate the effect of a Facebook-delivered weight-gain prevention program versus a Facebook-delivered program with general women's health information.

NCT ID: NCT02413866 Completed - Weight Clinical Trials

Weight Outlooks by Restriction of Diet and Sleep

WORDS
Start date: January 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to examine whether chronic moderate sleep restriction effects the amount of body fat and lean mass loss, and calorie expenditure, in individuals who are participating in a dietary weight loss program.

NCT ID: NCT02408692 Completed - Contraception Clinical Trials

Emergency Contraception and Body Weight: Pilot Study

Start date: February 2015
Phase: Phase 4
Study type: Interventional

The purpose of this research study is to determine how body weight changes the drug level of an emergency contraceptive pill containing a hormone called levonorgestrel (LNG). This emergency contraceptive is available to women without a prescription, but has recently been found to not work as well to prevent pregnancies in women of higher body weight. The overall goal of this research is to improve the effectiveness of contraception for women, no matter their weight.

NCT ID: NCT02404090 Not yet recruiting - Obesity Clinical Trials

Impact of the Excess Weight Loss on Mineralization Patterns of the Knee After Bariatric Operations

CT-OAM
Start date: August 2015
Phase: N/A
Study type: Observational

Evaluation of the subchondral mineralization plate after excess weight loss in patientes undergoing bariatric operation by means of CT-osteoabsorptiometry.

NCT ID: NCT02402985 Completed - Obesity Clinical Trials

Comparison of a Plant Protein Diet to a Animal Protein Diet Emphasized in Type 2 Diabetics

LeguAN
Start date: September 2013
Phase: N/A
Study type: Interventional

This 6-week parallel randomised prospective dietary intervention study with type 2 Diabetes investigates the nutrition influence of animal protein in comparison to plant protein on the glucose metabolism.

NCT ID: NCT02400398 Completed - Pancreatic Cancer Clinical Trials

Evaluating Weight Stability of Pancreatic Cancer Cachexia Patients

PanCax
Start date: April 27, 2015
Phase:
Study type: Observational

Eligible patients will have a diagnosis of both pancreatic adenocarcinoma and cachexia defined as greater than 5% unintentional weight loss within 6 months prior to screening visit. Patients must be greater than 18 years of age; and have greater than 3 months life expectancy. This study will observe a standard of care intervention (tube feeding) for potential benefit. Peptamen will be administered through a jejunal or a gastrojejunal feeding tube and dosing will be calculated using the Mifflin St. Jeor equation. It will be administered daily for the duration of the protocol.

NCT ID: NCT02399423 Completed - Obesity Clinical Trials

The GlasVEGAS Study (Glasgow Visceral & Ectopic Fat With Weight Gain in South AsianS)

GlasVEGAS
Start date: March 11, 2015
Phase: N/A
Study type: Interventional

South Asians have a much higher risk of diabetes compared to Europeans and investigators don't know why this is. Investigators think that South Asians' capacity to store fat safely under the skin is lower than Europeans, so they start to store fat around internal organs and in liver and muscle, and at lower body weights than Europeans. These increased levels of internal fat storage are thought to increase risk of diabetes. The purpose of the study therefore is to investigate whether there are differences with weight gain and weight loss in fat storage, fat cell function and metabolic risk factors, in South Asians compared with Europeans. Investigators will compare South Asian and European men at the start of the study, after they have gained about 7% body weight, and again after they have lost 7-15% body weight (from peak weight) to see how gaining and losing weight affects fat storage within the body and the function of fat cells. Investigators will also assess the effect of weight gain and weight loss on metabolism, fitness and risk factors for diabetes and heart disease.

NCT ID: NCT02396654 Completed - Fetal Weight Clinical Trials

5D LB Ultrasound in Determination of Fetal Weight in Normal Pregnancy : A Pilot Study

Start date: March 2015
Phase: N/A
Study type: Observational

5D and 2D ultrasound will be done to normal pregnant women between 37 to 42 weeks gestation and fetal weight will be estimated using the hadlock formula using biometry measured by both ultrasounds. Accuracy of 5D ultrasound in determining fetal weight will be determined.

NCT ID: NCT02395835 Completed - Body Weight Clinical Trials

Methylation of the PPARg Promoter Region in Pregnancy

Start date: September 2009
Phase: N/A
Study type: Observational [Patient Registry]

The main objective of this study was to assess whether clinical, anthropometric, and biochemical variables of the mother were associated with changes in the methylation of the PPARg promoter region (-351 to -260). Methodology: This was a matched cohort study with two groups: a) normal weight (NW) pregnant women (n = 21) and their offspring, and b) overweight (OW) pregnant women (n = 20) and their offspring. DNA was extracted from leukocytes (4000-10,000 cells) in the MagnaPure (Roche) using the MagNAPure LC DNA Isolation Kit 1 (Roche, Germany). The treatment of DNA (2 µg) was performed with sodium bisulfite (EZ DNA Methylation-Direct Kit, ZymoResearch). Real-time polymerase chain reaction (qPCR) was performed in a LightCycler 2.0 (Roche) using the SYBR® Advantage® qPCR Premix Kit (Clontech).

NCT ID: NCT02387671 Completed - Body Weight Clinical Trials

Weight Management Among Breast Cancer Survivors

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

The long-term goal of this research is to develop, evaluate and implement effective mHealth technology interventions that improve cancer management outcomes by changing lifestyle behaviors among urban health- disparity facing populations. To accomplish this goal, the investigators will need to determine the feasibility and preliminary efficacy of an intervention in which breast cancer survivors receive counseling about lifestyle behaviors (weight, nutrition, and physical activity) from a health counselor trained in evidenced-based behavioral counseling methods.