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Weight Loss clinical trials

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NCT ID: NCT02467036 Completed - Obesity Clinical Trials

Family Based Treatment for Weight Loss With Breakfast Prescription

FAB
Start date: January 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate whether a behavioral weight loss group in conjunction with a prescribed breakfast can help children between 8 and 12 years of age change their behaviors to help them lose weight and become healthier.

NCT ID: NCT02458053 Completed - Overweight Clinical Trials

Testing the Efficacy of a Spousal Support Enhanced Weight Loss Program on Weight Loss Among African American Men

TEAM
Start date: February 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the effect of a spousal support enhanced weight loss program on weight loss among African American men.

NCT ID: NCT02456636 Completed - Obesity Clinical Trials

Rural Engagement in Primary Care for Optimizing Weight Reduction

RE-POWER
Start date: February 15, 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to compare three methods for managing obesity in rural patients, to see which method will result in patients being able to attain their weight loss goal and maintain that weight loss.

NCT ID: NCT02451800 Completed - Obesity Clinical Trials

Exercise: Improving Compliance and Long-term Weight Loss

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

The overall aim of the proposed study is to determine the effectiveness of a 3-month yoga program on increasing compliance and improving weight loss while participating in the Sanford Profile program. Participants are randomized to one of three groups: in-class yoga, yoga by digital video disk (DVD), stretching by DVD. Changes in weight loss and stress levels are monitored.

NCT ID: NCT02449148 Completed - Obesity Clinical Trials

Nutrition and Energy Restriction for Cancer Prevention

HELENA
Start date: May 2015
Phase: N/A
Study type: Interventional

This study evaluates the effect of intermittent calorie restriction versus continued calorie restriction on weight loss, gene expression profile of subcutaneous adipose tissue and abdominal fat distribution.

NCT ID: NCT02445833 Completed - Obesity Clinical Trials

On-Line Intervention For Promoting Healthy Habits And Weight Loss In Hypertensive Patients

VIVIR-MEJOR
Start date: September 2014
Phase: N/A
Study type: Interventional

Efficacy of an Internet-based self-guided intervention for promoting healthy habits and weight loss in hypertensive people with overweight and obesity: A Randomized Controlled Trial

NCT ID: NCT02437643 Completed - Obesity Clinical Trials

An Enhanced Protein (Dairy) Weight Loss Intervention for Dynapenic Obesity: Impact on Muscle Quality and Composition

DDYNAMO
Start date: August 17, 2015
Phase: N/A
Study type: Interventional

The purpose of the trial is to assess the effects of combining regular, generous intakes of high quality protein (primarily from dairy and other animal source proteins) with calorie restriction and low-intensity exercise on muscle quality and muscle adipose infiltration (along with bone mineral density [BMD] and a number of secondary outcomes) in frail, obese, older adults participating in a 6 month intervention. The investigators will compare these effects to those of a traditional control regimen of calorie restriction and low-intensity exercise over the same duration.

NCT ID: NCT02421406 Completed - Obesity Clinical Trials

An Internet-based Behavioral Weight Loss Program for HIV+ Patients

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

The goal of this project is to determine whether an Internet-based weight loss program will lead to weight loss and improvements in cardiovascular disease risk factors in people living with HIV.

NCT ID: NCT02419092 Completed - Obesity Clinical Trials

Obstructive Sleep Apnea-induced Changes in Adipose and Liver Tissue and Effects of Massive Weight Loss on Inflammation

Start date: April 2015
Phase: N/A
Study type: Observational

UPDATED May 2016: Originally the study design included investigation of the effects of the bioactive compound resveratrol compared to placebo tablets and to CPAP treatment. Due to fewer subjects having OSA than estimated by pre-study and, therefore, difficulties in the recruiting process the investigators have found it necessary to descale the study design. Hence, we have discontinued the resveratrol and CPAP intervention and will focus on the cross-sectional investigation of metabolic changes in subjects with and without OSA and the effect of weight loss after bariatric surgery on inflammation, OSA severity, metabolism and arterial stiffness. Obstructive sleep apnea (OSA) is a common disorder especially among obese individuals and patients with type 2 diabetes. OSA is associated with an increased morbidity and mortality. Continuous positive airway pressure (CPAP) is the standard treatment. Also weight loss is known to reduce the severity of OSA, especially bariatric surgery has proven effective because of the massive weight loss. The investigators hypothesize that OSA via pro-inflammatory responses in various tissues causes low-grade inflammation which ultimately induce the associated co-morbidities. The investigators hypothesize that massive weight loss after bariatric surgery have beneficial effects on severity of OSA, inflammatory status and improves insulin sensitivity.

NCT ID: NCT02418546 Completed - Parkinson's Disease Clinical Trials

Electronic-health Application To Measure Outcomes REmotely Clinical Trial

EAT MORE
Start date: April 2015
Phase: N/A
Study type: Interventional

This is a phase II feasibility, safety, tolerability and preliminary efficacy study of an e-Health application versus in-person nutritional counseling to maintain or increase weight in patients with neurodegenerative diseases including amyotrophic lateral sclerosis (ALS), Parkinson's Disease (PD) and Huntington's disease (HD). Primary Objectives include the feasibility, safety, tolerability and efficacy of an e-Health application to maintain or increase body weight compared to in-person nutritional counseling. Secondary Objectives are to measure the number of calories required to maintain or increase body weight in neurodegenerative diseases at all stages of the disease. Tertiary Objectives are to test the effects of an e-Health application compared to in-person nutritional counseling on disease progression using the ALSFRS-R, UHDRS or UDysRS, on survival, and on quality of life using the PROMIS SF v1.1 scale.