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Body Weight Changes clinical trials

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NCT ID: NCT06127511 Not yet recruiting - Inflammation Clinical Trials

Peanut Consumption on Cognitive, Weight, and Inflammation

PEANUTY
Start date: January 2024
Phase: N/A
Study type: Interventional

A multi-school, two-arm parallel cluster-randomized controlled trial will be conducted in 200 healthy young adolescents from Barcelona (Spain) to evaluate the effect of peanut consumption on cognitive performance, weight management and inflammation. Schools willing to participate will be randomly assigned to either the intervention or the control group. After the recruitment, the participants will follow a peanut-free diet for two weeks. Both arms will receive a multidimensional educational intervention designed by the Gasol Foundation to promote healthy dietary habits based on Mediterranean diet recommendations, along with exercise performance, healthy sleeping habits and emotional knowledge. Half of the participants (intervention group) will consume 25 g of whole skin roasted peanuts as a daily snack to be incorporated into their diet for six months.

NCT ID: NCT06046755 Not yet recruiting - Breast Cancer Clinical Trials

Nutritional Intervention-induced Weight Loss During the Oncological Treatment of Obesity-related Breast Cancer

NUTOBREST
Start date: October 15, 2023
Phase: N/A
Study type: Interventional

Obesity could become the first evitable cause of breast cancer in the near future. Due to the relatively slow rate of development in this field, greater efforts must be applied in this area. The HYPOTHESIS of this work is that "a therapy to lose weight in breast cancer women with obesity during the oncological treatment could contribute to slowing carcinogenesis, and to improve the response to the chemotherapy, survival and prevent future recurrences by erasing deleterious epigenetic marks". A group of breast cancer women with obesity (n=90) will be treated to lose weight during the oncologic treatment with a low calorie-ketogenic diet or a group educational intervention program of healthy lifestyle. The reversibility of the obesity-related breast cancer epigenetic signatures (EPIC array and pyrosequencing) and other molecular features (QRTPCR, ELISA assays) in blood leukocytes and plasma and the progression of disease will be compared with an obesity (n=30) and normalweight (n=30) group under conventional anticancer therapy. A matched-group of tumor-free women (n=60) with obesity will be also treated to lose weight with the same nutritional interventions and compared with tumor-free women with normal weight (n=30) in order to evaluate the potential preventive function of weight loss therapies on cancer-related odds. The outcomes of this project will directly benefit overweight and obese patients from healthcare systems, and also to have an economic value supporting pharmaceutical and food industry companies in the design of innovative treatments, useful biomarkers and preventive tools.

NCT ID: NCT06024161 Not yet recruiting - Obesity Clinical Trials

Weight Change and the Risk of Chronic Pain Following Hip and Knee Arthroplasties

Start date: November 1, 2023
Phase:
Study type: Observational [Patient Registry]

The study is a nationwide, register-based cohort survey study. The objective of this study is to investigate whether weight change is associated with the incidence of persistent postoperative pain following total hip arthroplasty and knee arthroplasty across non-obese and obese and patients.

NCT ID: NCT05644717 Not yet recruiting - Liver Fibrosis Clinical Trials

Effect of Erugliflozin On Liver Fat, Liver Fibrosis and Glycemic Control in Type II DM Patients With NASH/NAFLD

Ertu-NASH
Start date: March 1, 2023
Phase: Phase 4
Study type: Interventional

Open-label, prospective, single-arm, multicenter study to determine effects of Ertugliflozin on liver fat, liver fibrosis & glycemic control in subjects with Type 2 Diabetes Mellitus (T2DM) with Non-Alcoholic Fatty Liver Disease (NAFLD)/Non-Alcoholic Steatohepatitis (NASH)

NCT ID: NCT05616052 Not yet recruiting - Weight Change, Body Clinical Trials

Comparison of Body Weight Change Through Different Smeglutide Administration Methods

Start date: December 1, 2022
Phase: Phase 4
Study type: Interventional

Investigators determined to detect the effect of smeglutide on body weight and metabolic indexes among overweight and obese participants through two different dosing programs.

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: NCT03436277 Not yet recruiting - Body Weight Changes Clinical Trials

Effect of the Administration of L-Carnitine on Body Weight in Women in Crossfit Training

Start date: December 17, 2018
Phase: Phase 2
Study type: Interventional

The L-carnitine has demonstrated effects in the treatment of obesity mainly promoting the fat degradation during exercise.

NCT ID: NCT03196453 Not yet recruiting - Overweight Clinical Trials

Fit Child - Clinical Study on Weight Control

FITCHI
Start date: August 1, 2017
Phase: N/A
Study type: Interventional

Children with abnormal weight development of BMI will be given either placebo or a probiotic protein formula and measures of weigh gain during a 3-mont treatment will be conducted

NCT ID: NCT02715895 Not yet recruiting - Body Weight Changes Clinical Trials

Clinical Trial of Infant Formula-fed

Start date: April 2016
Phase: N/A
Study type: Interventional

Compared with breast milk and another commercially available formula, infants' growth rate after 12 weeks' Friso formula with different ways of processing feeding will be assessed.

NCT ID: NCT01989871 Not yet recruiting - Breast Feeding Clinical Trials

Adjusted Individual Oral Feeding for Improving Short and Long Term Outcomes of Preterm Infants

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

The authors hypothesize that adjusted individual feeding (AIF) for preterm infant starting from transition to oral feeding (33 weeks corrected age) will result in less episodes of apnea/bradycardia, early achievement of full oral feeding, improved weight gain and shorten hospitalization duration in the short term. In the long term AIF will result in higher scores on the Griffith's developmental scales, decreasing parental anxiety and feeding disorders .