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Body Composition clinical trials

View clinical trials related to Body Composition.

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NCT ID: NCT02440503 Completed - Body Composition Clinical Trials

How Infant Diets Would Affect Growth in Early Childhood

FYI-FU
Start date: June 2014
Phase: N/A
Study type: Observational

The investigators research group conducted a feeding study in 2012 (IRB 07-0003) that included breastfed infants consuming different infant solid foods. The investigators results showed that different solid foods, especially the protein content of the food, is important on infant's gut bacteria profile and growth. Although the first year of life is critical in obesity development later in life, data are very limited on the effect of protein from solid foods, an important component of infant diet, especially in breast-fed infants. In this study, the investigators will re-contact these participants, who are now in their early childhood (~5 years old), to evaluate the long-term effect of various macronutrient quantities in solid foods, by assessing the participants' growth, body composition, and gut bacteria profile.

NCT ID: NCT02383017 Completed - Body Composition Clinical Trials

Effects of Shroom Tech Sport Supplementation and Concurrent Training

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

This study will examine how the supplement Shroom Tech Sport (STS) affects body composition and different performance and health measures over the course of 12 weeks. The supplement will be combined with a concurrent training regime consisting of resistance and high intensity interval training. Subjects will be tested for percent body fat to determine body composition. Further, they will also be tested for maximal strength (squat and bench), maximal power output and fatigue, lactate threshold and maximal oxygen volume consumption (VO2max). And finally, subjects will be tested for health and hormone markers in the blood. All of these measures will be compared against a placebo group participating in the same exercise intervention.

NCT ID: NCT02380664 Active, not recruiting - Body Composition Clinical Trials

Swimming Training Repercussion on Metabolic and Structural Bone Development; Benefits of the Incorporation of Whole Body Vibration or Plyometric Training: The RENACIMIENTO Project

Start date: January 2012
Phase: N/A
Study type: Interventional

Swimming training is associated with decreased bone mass and lower bone mass acquisition during growth periods, mainly when compared to other weight-bearing sports. Little information is available in adolescents pointing in the same direction but still controversial. On the other hand, bone strength do not only depends on bone mass but on bone structure and microarchitecture. The cross sectional area, cortex thickness or trabecular density are important aspects of bone health. There are few studies on the effect of swimming on bone architecture of adolescents. This information is relevant for present and future health of adolescents practicing swimming and for all the organizations promoting this sport. Jumping and whole body vibration training programs seem to elicit important osteogenic effects; however, there is little information on this regard in adolescent population, even less in these adolescents with potentially decreased bone acquisition such as swimmers. The main aims of this research project are therefore, to analyze the effect of swimming training on bone mass, metabolism, structure and architecture in adolescents analyzing possible relationships among them. Secondly, to test whether including short boots of jumping or whole body vibration may be able to palliate the possible deleterious effects of swimming and facilitate a normal or even healthier bone development. And finally to study the durability of training-related bone gains over time.

NCT ID: NCT02211612 Completed - Obesity Clinical Trials

Overeating Different Fats and Influence on Muscle Mass and Body Fat Accumulation

LIPOGAIN-2
Start date: September 2014
Phase: N/A
Study type: Interventional

To investigate metabolic and molecular response to fatty acid-specific overfeeding in overweight subjects, in relation to changes in ectopic fat, lean tissue mass and insulin sensitivity

NCT ID: NCT02126410 Completed - Sleep Clinical Trials

Associations Between Self-Reported Sleep Duration and Sarcopenia in Community-Dwelling Older Adults

Start date: March 2014
Phase: N/A
Study type: Observational

1. BACKGROUNDS: Currently, elderly people comprise more than 10% of the total Taiwanese population. However, within the context of self-reported sleep duration and health risks, research into the association between sleep duration and body composition changes in older people is limited. It is important to gain an understanding of such an association of older people to estimate the public health burden. 2. OBJECTIVES: To assess the association between self-reported sleep duration and sarcopenia as well as obesity in community-dwelling older adults. 3. HYPOTHESIS: Self-reported sleep duration is associated with prevalence of sarcopenia and obesity in community-dwelling older adults. 4. DESIGN: A cross-sectional investigation. 5. SETTING: Communities in Zhongzheng district, Taipei. 6. PARTICIPANTS: Four hundred and forty-eight community-dwelling adults (224 men and 264 women) aged 65 years and older. 7. MEASUREMENTS: The investigators evaluated self-reported sleep duration by deriving from the Pittsburgh Sleep Quality Index and 7-d recall physical activity diary. Skeletal muscle mass was estimated by the predicted equation from a bioelectrical impedance analysis measurement. The Groningen Activity Restriction Scale and the Chinese Geriatric Depression Screening Scale were used to evaluate physical disability and depression, respectively.

NCT ID: NCT02118675 Completed - Body Composition Clinical Trials

Tanita BIA System Validation

Tanita
Start date: January 2014
Phase: N/A
Study type: Observational

The study is to collect the body composition data using five different methods-bioimpedance analysis (Tanita®), DXA (GE Medical), BodPod (Life Medical), deuterium dilution (heavy water), body circumferences (tape measure, TC2), and tissue thickness by ultrasound (GE Medical, BodyMetrix).

NCT ID: NCT02115425 Completed - Body Composition Clinical Trials

Calibrate Samsung's BIA to Meseaure Body Composition

Samsung
Start date: April 2014
Phase: N/A
Study type: Observational

The purpose of this study is to collect body composition data using bioimpedance analysis (Samsung) and DXA (GE Medical). Both of the methods are explained in more detail in section 5 of this consent. The data collected will help Samsung improve the products the company offers.

NCT ID: NCT02000492 Completed - Body Composition Clinical Trials

Frequent Ballgames Training for 9-11 Year Old Schoolchildren

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

Inactivity among schoolchildren is a challenge to public health and for the municipality in particular. This study´s aim is to evaluate the cognitive and physical as well as social and fitness adaptations, and learning outcomes of short- and long term ball training for 9-11 years old girls and boys, and to determine to what extend the organisation (5x12 minutes og 3x40 minute a week) and type of training (ball games, circuit training or running) influence the magnitude of response.

NCT ID: NCT01945320 Recruiting - Malnutrition Clinical Trials

The Effects Nutrition Status and Body Composition on HD Patients' Outcome

Start date: March 2012
Phase: N/A
Study type: Observational

A prospective long-term follow up of hemodialysis (HD) patients' outcome correlates with nutritional status and body composition. We will evaluate the body composition change among HD patients every three months with bioelectrical impedance analysis (BIA). The change of body composition will correlated with other clinical data including nutritional, inflammatory parameters and survival.

NCT ID: NCT01918319 Completed - Childhood Obesity Clinical Trials

Lifestyle in Pregnancy and Offspring

LiPO
Start date: February 2011
Phase: N/A
Study type: Interventional

Children born to obese women are at risk of increased adiposity and later adverse metabolic outcomes. We have conducted a follow-up study on an existing clinical trial, called the LiP study (Lifestyle in Pregnancy), registration number NCT00530439,in which 360 obese pregnant women were randomized to either lifestyle intervention or routine obstetric care. This present study follows the children until 3 years of age. We have the hypothesis, that the intervention during pregnancy results in a lower degree of adiposity and metabolic risk factors in the offspring. Clinical examination is taking place at age 2.5-3 years including anthropometric measurements, Dual energy x-ray (DXA) scans and blood samples measuring metabolic markers.