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Overweight clinical trials

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NCT ID: NCT04323995 Completed - Clinical trials for Overweight and Obesity

Efficacy of Sprint Interval Training on Anthropometric Measures

Start date: March 2, 2020
Phase:
Study type: Observational

Due to the rising problem of overweight and obesity, many strategies are implemented to combat this issue and one of the most common ways is exercise training. Aerobic exercise is a popular and effective conservative strategy for weight and adiposity management and commonly used exercise protocols are moderate-intensity continuous training (MICT) and interval training (IT). MICT is typically defined as continuous effort that elicits 55%-70% of the maximal heart rate or promotes oxygen consumption equivalent to 40%-60% of the maximum oxygen intake. IT involves repeated exercise with periods of recovery, which includes high intensity interval training (HIIT) and Sprint interval training (SIT). HIIT is exercising at 80% to 100% of maximal heart rate while SIT involves "all-out" or "supramaximal" effort at the intensity of 100% of maximal oxygen uptake. Multiple systematic reviews on the effect of SIT on aerobic capacity or comparisons between other forms of exercise protocols to reduce body adiposity has been conducted, but so far no systematic review has been carried out to evaluate the efficacy of this protocol solely on anthropometric measures on young obese and overweight adults alone. Hence, in this study, a systematic review of the effect of SIT on anthropometric measurements in young obese or overweight adults will be reviewed, filtered and assembled.

NCT ID: NCT04321590 Completed - Clinical trials for Overweight and Obesity

Efficacy of Hydroxycinnamates and Beta-glucans as a Dietary Tool Against obesity_Pilot Study (OBHEALTH_PS)

OBHEALTH_PS
Start date: September 11, 2017
Phase: N/A
Study type: Interventional

Randomized, double blind, parallel study to assess the effect of a dietary supplement combining polyphenols (hydroxycinnamates from green coffee) and a soluble dietary fiber (oat beta-glucans) in obese/overweight subjects.

NCT ID: NCT04318288 Completed - Obesity Clinical Trials

Comparison of Anthropometric Parameters and Cardiometabolic Risk Factors Among Subjects With Overweight and Obesity

Start date: January 7, 2019
Phase:
Study type: Observational

The study was aimed at comparing four different anthropometric parameters to cardiometabolic risk factors in overweight and obese subjects (Body Mass Index (BMI)≥25)

NCT ID: NCT04317079 Completed - Body Weight Clinical Trials

Effects of Hydroxytyrosol Administration in Anthropometric Parameters in Overweight and Obese Women

Start date: October 30, 2017
Phase: N/A
Study type: Interventional

This study aims to investigate the potential effects of the administration of hydroxytyrosol, which is an extra virgin olive oil phenolic compound, in doses 15 milligrams and 5 milligrams daily versus placebo for 6 months in anthropometric parameters such as body weight, body fat and visceral fat, in combination with diet, in overweight and obese women.

NCT ID: NCT04315220 Completed - Childhood Obesity Clinical Trials

Corestability Training in Overweight Children

Start date: October 13, 2020
Phase: N/A
Study type: Interventional

A total of 52 overweight children aged between eight and sixteen years will be recruited by criterion based purposive sampling to participate in the two groups pretest post test randomized clinical study. Random allocation of the eligible subjects for treatment will be done by the block randomization method with matrix of thirteen rows and four columns (13x4). The subject will be allotted to the group randomly, based on the chit selected by the person other the primary researcher.Once the block is filled, the next row block will be opened. Thus equal distribution of overweight children in the each group will be ensured. Group A will be receiving actual core stability training (Level 1 - Mat exercises and Level 2 - Swiss Ball exercises) for 6 weeks with a frequency of three sessions per week.Group B will receive no training. Each session will last for 30 minutes of duration. The static and dynamic balance, foot pressure distribution and core strength will be assessed at the baseline and at the end of the treatment sessions.

NCT ID: NCT04311450 Completed - Clinical trials for Overweight and Obesity

Behavioral Weight Loss Treatment for Individuals With Food Addiction

FA Pilot
Start date: March 1, 2021
Phase: N/A
Study type: Interventional

The purpose of this research study is to examine how well an existing weight loss treatment works for individuals with food addiction. Treatment will consist of a preliminary 12-week RCT pilot of the feasibility and effectiveness of behavioral weight loss (BWL) compared to a waitlist control.

NCT ID: NCT04311411 Completed - Obesity Clinical Trials

A Study of Tirzepatide in Overweight and Very Overweight Participants

Start date: August 24, 2020
Phase: Phase 1
Study type: Interventional

The main purpose of this study is to measure the effect of tirzepatide on food intake in participants who are overweight or very overweight. The study will also use imaging to learn more about how tirzepatide affects specific parts of the brain. The effect of tirzepatide on appetite will also be studied. The study will last up to about four months and will include up to 14 visits to the study center.

NCT ID: NCT04307212 Completed - Overweight Clinical Trials

How Exercise Signals Health Responses

Start date: January 10, 2020
Phase: N/A
Study type: Interventional

The purpose of this research is to determine the blood signals that promote health and well-being in response to exercise at different intensities.

NCT ID: NCT04300478 Completed - Breast Cancer Clinical Trials

Appetite and Exercise in Breast Cancer Survivors

EARNESt
Start date: February 7, 2020
Phase: N/A
Study type: Interventional

The overall aim of this research is to investigate the acute effects of resistance exercise (REx) on the hormonal and behavioral indices of energy balance regulation in breast cancer survivors. This pilot study is designed to provide preliminary data to support future exercise interventions with more comprehensive energy balance profiling.

NCT ID: NCT04298944 Completed - Hypertension Clinical Trials

Association of Mood With Risk for Atherosclerosis

AuRA
Start date: March 11, 2020
Phase:
Study type: Observational [Patient Registry]

The investigators will aim to determine the association of mood disorders (MDO) with preclinical and clinical cardiovascular (CVD) risk factors among children. The investigators will also aim to identify traditional and non traditional predictors of CVD risk among children with MDO.