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Body Weight Changes clinical trials

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NCT ID: NCT04464278 Not yet recruiting - Body Weight Changes Clinical Trials

Variation in Body Composition on the Fate of Older Subjects During SSR Hospitalization

VALCOR
Start date: July 2020
Phase:
Study type: Observational

The aim of this study is to correlate weight variation as well as body composition with mortality and unscheduled readmission of geriatric population

NCT ID: NCT04434079 Completed - Critical Illness Clinical Trials

Fluid Balance and Body Weight Changes in Critically Ill Adult Patients

Start date: June 1, 2018
Phase:
Study type: Observational

Positive fluid status has been consistently associated with worse prognosis in critically ill adult patients.However, observational studies showed poor agreement between fluid balance and body weight changes. The objective of the study is to compare the measurements of FB and BW over time and to assess correlation with ICU mortality.

NCT ID: NCT04429581 Completed - Body Weight Clinical Trials

Differences in Fat Mass Estimation Formulas in Physically Active Adult Population and Relation With Skinfold Sums.

Start date: February 2, 2013
Phase:
Study type: Observational

The objective of the present study was to analyze the differences between the formulas used to estimate fat mass and to establish the existing relationship with the skinfold sum in anthropometry. A total of 2,458 active subjects participated in the study (mean age: 27.98±7.43 years-old). Basic measurements and skinfolds variables were measured following the guidelines of the International Society for the Advancement in Kinanthropometry (ISAK), and Kerr, Durnin-Womersley, Faulkner and Carter equations were used to assess fat mass. Significative differences were found between all the formulas for the percentage of fat mass and the fat mass in kilograms. The correlations among the skinfolds sums and the different equations were high and significative in all the cases. There were differences between all the formulas used to estimate the fat mass. The six or eight skinfold sums could be a valid and better alternative than the fat mass equations or the BMI to assess the subcutaneous fat mass in physically active adults.

NCT ID: NCT04417582 Recruiting - Obesity Clinical Trials

Life Style Modification Medical and Surgical Management in Patients With Obesity

Start date: January 1, 2020
Phase:
Study type: Observational [Patient Registry]

In this is an observational study, obese patients that administed and followed in endocrinology clinic of Marmara University Medical school hospital will follow for clinical and laboratory parameters prospectively for 5 years

NCT ID: NCT04373434 Completed - Weight Change, Body Clinical Trials

Healthy Homes/Healthy Families (HH/HF) Intervention in 2-1-1 Callers

Start date: September 18, 2020
Phase: N/A
Study type: Interventional

This trial will evaluate a healthy eating and weight gain prevention intervention for delivery through calls to the 2-1-1 number.

NCT ID: NCT04348019 Completed - Blood Pressure Clinical Trials

Effects of a Daily Time-Restricted Feeding Protocol on Diet Quality

Start date: October 11, 2019
Phase: N/A
Study type: Interventional

As a result of unhealthful lifestyle practices including nighttime ingestion and excess energy-dense food and beverage intake, college students are presenting with metabolic abnormalities and excess weight gain that increases their risk for chronic health conditions including cardiovascular diseases and type 2 diabetes. Research has shown that prolonging nightly fasting intervals can result in health improvements in both animal models and human subjects. Time-restricted feeding (TRF), a form of intermittent fasting may offer an exciting, non-pharmacologic approach to improve cardiometabolic health in this population by restricting food intake to feeding windows that align with circadian biology.

NCT ID: NCT04340388 Completed - Vascular Diseases Clinical Trials

Contribution of Dolutegravir to Obesity and Cardiovascular Disease

Start date: September 17, 2020
Phase: Phase 4
Study type: Interventional

The goal of the study is to combine a collaborative and translational approach to evaluate the effect antiretroviral regimen switch to a dolutegravir containing regimen compared to continued treatment with a non- dolutegravir based regimen on on lipid and metabolic profiles, renal function, body composition, vascular function and diet.

NCT ID: NCT04289168 Completed - Body Weight Changes Clinical Trials

Infant Peer Interaction Study by Examining the Effect of a 6-week Music Enhancement Program

Start date: August 11, 2014
Phase: N/A
Study type: Interventional

The overall purpose of this study is to better understand food reinforcement in infants. The results of this study should help to further our understanding of how individuals relate to food and how an enriched environment can change this behavior.

NCT ID: NCT04230824 Completed - Body Weight Changes Clinical Trials

Chronic Study on Body Composition, Training, Performance, and Recovery

Start date: February 1, 2021
Phase: N/A
Study type: Interventional

The chronic phase of the study will evaluate the effects of pre-exercise and post-exercise ingestion of a multi-ingredient supplement on adaptations to a 6-week exercise program consisting of both resistance training and high intensity aerobic exercise, using a randomized, double-blind, placebo-controlled design. Participants will complete an enrollment/familiarization visit, a baseline testing session, followed by a 6-week supervised exercise intervention, and post-testing session identical to baseline testing. Participants will be randomized during the baseline session to groups receiving either 1) Active Treatment (pre-post supplementation), 2) placebo (noncaloric beverage), or 3) control, not participating in exercise or consuming a treatment. During the supervised 6-week resistance training program, participants will complete a moderate-intensity warm-up, a full-body resistance training workout (2 x per week) and an interval training session (1 x per week). Thirty-minutes prior to each training session, and within 15 minutes post-exercise, participants will consume their randomly assigned treatment beverage. Body composition, blood markers of muscle damage/recovery, strength, and performance tests will be measured before (baseline) and after training (Post) to evaluate the effects of supplementation. All data collection will be conducted by the Principal Investigator and Research Assistants. All subjects will report to the Applied Physiology Laboratory and Human Performance Center in Fetzer Hall for all testing and training sessions, which will span approximately 8 weeks.

NCT ID: NCT04201028 Completed - Obesity Clinical Trials

A Remote Delivered Lifestyle Therapeutics Program

Start date: January 6, 2021
Phase: N/A
Study type: Interventional

Heart disease is the leading cause of death in the United States. The overall risk for heart disease is a composite measure of various modifiable factors including blood pressure, cholesterol, and tobacco use; which are exacerbated by a sedentary lifestyle, unhealthy diet, and being overweight. Approximately 32% of the adult U.S. population has high blood pressure and 46% of them have uncontrolled hypertension. Successful management of high blood pressure and other cardiovascular risk is a complex process that requires significant lifestyle changes but adopting and adhering to these changes is challenging. A promise approach to overcoming these challenges is utilizing health coaching. The purpose of this research study is to compare at home devices for blood pressure and weight measurements (DEV) group compared to not using any at home devices Group (NODEV). Both groups will be supported throughout this study by meeting with obesity medicine doctor monthly in office and have a virtual health coaching visits throughout the study duration.