Clinical Trials Logo

Body Composition clinical trials

View clinical trials related to Body Composition.

Filter by:

NCT ID: NCT04136821 Completed - Oxidative Stress Clinical Trials

The Long-term Effects of Oceanix™ on Resistance Training Adaptations

Start date: September 30, 2019
Phase: N/A
Study type: Interventional

This study will examine the effects of Oceanix™, an antioxidant supplement, on muscle performance, immune and endocrine function, recovery and safety in participants undergoing resistance training. Measures of muscle performance will include isometric testing in the bench-press and mid-thigh pull and ground reaction forces in the counter movement- and squat-jump. Markers of immune function will include salivary immunoglobulin A (IgA) as well as serum total antioxidant capacity (TAC) and superoxide dismutase (SOD) while endocrine function will be measured by salivary cortisol and testosterone. Recovery will be measure by plasma creatine kinase (CK) and perceptual measures will be assessed using a validated perceived recovery status (PRS) scale. Safety metrics will be indicated by a comprehensive metabolic panel (CMP), complete blood count (CBC), and urinalysis (UA). Additionally, the modified Borg Rating of Perceived Exertion (RPE) will be administered following each training session to grade physical exertion and monitor progression of the training protocol.

NCT ID: NCT04076592 Completed - Breastfeeding Clinical Trials

NUTRIPROTECT-Children Nutrition as a Protective or Health-risk Factor

My-Milk-2
Start date: February 1, 2018
Phase:
Study type: Observational

Despite the intensive worldwide research dedicated to the nutrition and faecal microbiota, the studies that follow the link between the early nutrition, initial intestinal microbiota, and development of children over a longer time period are limited. From 2010 to 2013, the investigators conducted a study "My-Milk" in Slovenia. From 185 participating pregnant women involved in the detailed part of the protocol (comprising of 4-days weighed dietary record, visits at clinic and biological sample collection), 152 participants completed the study at the child's first year of age. Five of the participants bore twins whose data was excluded from the research because infant's identity was not consistently followed throughout the research. In addition to studying the microbiota and fatty acid composition of breast milk and the initial development of intestinal microbiota of breastfed babies, the investigators also monitored the diet of expecting and nursing participants, concentration of vitamin D in serum and bone mineral density in participating mothers and children. The investigators performed anthropometric measurements of children during the first year of age. All singleton children who have completed My-Milk study (N= 147) will be invited in the follow-up study "My-Milk-2". The first step of the proposed study will be the evaluation of nutritional status of children aged 6 to 7 years in 2017/2018, including the assessment of the body composition (bone density, percentage of fat and muscle tissue), health indicators (blood pressure, blood cholesterol, frequency and severity of infections) and fecal microbiota. The obtained data of My-Milk and My-Milk-2 studies will enable the prospective cohort study to be carried out on the effects of early nutrition and various factors of mother and child during the first year of age on the health and developmental status of children aged 6- 7 years. The project results will significantly improve the progress in research areas of public health and nutrition. The interactions along the axis nutrition in early childhood, gut microbiota composition/ diversity and potential health problems in later life are still not fully explored. The investigators expect the results of the proposed study will contribute to the scientific development in this field in global prospective. The acquired information will also be an excellent basis for development of new dietary guidelines for children.

NCT ID: NCT03884010 Completed - Body Composition Clinical Trials

Accuracy of Anthropometric Equations to Estimate DXA-Derived Skeletal Muscle Mass in Professional Male Soccer Players

Start date: August 2009
Phase:
Study type: Observational

This study aimed to analyze the accuracy of different anthropometric equations to estimate skeletal muscle mass in professional male soccer players, setting dual-energy x-ray absorptiometry (DXA) skeletal muscle mass as the reference.

NCT ID: NCT03883997 Completed - Body Composition Clinical Trials

Accuracy of Anthropometric Equations for Estimating Body Fat in Professional Male Soccer Players Compared With DXA

Start date: August 2009
Phase:
Study type: Observational

This study aimed to analyze the accuracy of different anthropometric equations to estimate body fat in professional male soccer players, setting DXA body fat as the reference.

NCT ID: NCT03828812 Completed - Blood Pressure Clinical Trials

Temporal Patterns of Diet and the Changes in Body Composition and Blood Pressure

Start date: August 1, 2015
Phase: N/A
Study type: Interventional

The study includes two parts: 1) an observational study examines the association of meal frequency, meal timing, and meal regularity with short-term changes in blood pressure and body composition; 2) a randomized controlled intervention examines the influence of recommendation of increase breakfast frequency and decrease nighttime snacking on 1-year changes in blood pressure and body composition.

NCT ID: NCT03759951 Completed - Body Composition Clinical Trials

Hybrid Exercise Training for Health, Performance and Well-Being (DoIT II)

Start date: July 1, 2019
Phase: N/A
Study type: Interventional

Observing a lack of research investigating the chronic physiological and psychological responses to this type of exercise training the aim of this study is to investigate the optimal training configurations of DoIT to produce positive effects on health, performance and quality of life markers in sedentary overweight or obese adults aged 30-55 years. The DoIT program will be performed in a small-group setting indoor or outdoor implementing a progressive manner for 12 months and using bodyweight exercises with alternative modes.

NCT ID: NCT03749200 Completed - Metabolic Syndrome Clinical Trials

Motivational Approach to Treat Childhood Obesity

OBEMAT20
Start date: January 1, 2016
Phase: N/A
Study type: Interventional

The treatment of childhood obesity is challenging. Although dietary and physical activity recommendations are widely known, the willingness to change lifestyles within the family is not easy to be achieved. Motivational interviewing has been shown as a possibly effective method to increase adherence to dietary recommendations in the obese adult. There is scarce evidence showing whether implementing a motivational interview in obese children could be effective. The aim of this clinical trial is assessing the effect of a motivational interview, coordinated between the clinical and primary care services on 8 to 14 years old obese children.

NCT ID: NCT03722602 Completed - Stroke Clinical Trials

Body Composition of People After a Stroke

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

The study enabled assessment of changes in body mass composition, metabolic syndrome and lipid profile in patients after stroke, following rehabilitation in hospital.

NCT ID: NCT03683238 Completed - Clinical trials for Vitamin D Deficiency

Nutritional Status and Hidradenitis Suppurativa (Acne Inversa)

NutriHidra
Start date: May 2015
Phase:
Study type: Observational

Hidradenitis suppurativa (HS) is a chronic inflammatory, debilitating skin disorder. The exacerbating factors of HS include nutrition and adiposity. The objective of this study was to investigate the relationships between body composition and the adherence to the Mediterranean diet (MD) with the severity of HS in a sample of naïve-treatment patients with HS. In the wake of this evidence, in the study to investigate the relationships between nutritional status, the adherence to the MD, body composition, and the severity of HS in a sample of naïve-treatment patients with HS compared to control group matched for sex, age, and body weight.

NCT ID: NCT03603041 Completed - Sleep Clinical Trials

Nutrition, Body Composition, and Sleep

SHAPE
Start date: July 16, 2018
Phase: N/A
Study type: Interventional

The purpose of the research is to determine if protein and omega-3 fatty acid supplementation improve sleep, improve body composition, and improve markers of metabolic health in postmenopausal women.