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Active clinical trials for "Weight Loss"

Results 361-370 of 1462

Loss of Control Eating Following Weight Loss Surgery

Loss of Control Eating

This study will test the effectiveness of two distinct behavioral treatments for loss of control eating following bariatric surgery: Behavioral Weight Loss Treatment Cognitive Behavioral Therapy These treatments will be compared to Standard-of-Care.

Completed11 enrollment criteria

Behavioral Activation for Smoking Cessation and the Prevention of Post-Cessation Weight Gain

Smoking CessationWeight Loss

The purpose of this research study is to better understand (1) why people gain weight when they quit smoking and (2) whether certain types of smoking cessation (i.e. quit smoking) counseling combined with the nicotine patch help people quit smoking and gain less weight.

Completed54 enrollment criteria

Examining Reach and Implementation of an Evidence-based Weight Loss Program in Rural Primary Care...

Obesity

The majority of American adults do not meet recommended guidelines for healthy eating or physical activity and are overweight or obese, which puts them at risk for chronic disease, poor quality of life, and increased personal and public health care costs. Despite the development and success of a number of evidence-based weight management interventions, these programs have lacked systematic and consistent translation in clinical practice or community services. Further, few of these interventions have been tested in rural populations, where there is a disproportionally high number of obese individuals, and resources to support such programs are lacking. Primary care clinics have the necessary resources to support such programs, and might be the ideal setting to intervene and address concerns of weight loss and management in rural areas. The intent of the proposed project is to increase the capacity of primary care in rural Nebraska to translate evidence-based weight management approaches into practice, improve the speed of uptake and the likelihood of sustainability, and reach a large and representative group of individuals. To achieve this, the investigators will 1) conduct a limited effectiveness and feasibility study to determine impact on weight loss of 100 overweight and obese adult patients in a rural Nebraska primary care clinic, and 2) test multiple strategies for recruitment to determine best practices for program reach. The primary outcome for program effectiveness is percent body weight loss, and the primary outcome for program feasibility is reach, defined as the proportion of individuals who enroll in the program per each recruitment strategy. The proposed project provides a means of implementing an evidence-based weight loss program in rural Nebraska, has the capacity to create meaningful change in patient weight status, and has the potential to influence future efforts to translate evidence-based weight management programs into rural primary care practice.

Completed18 enrollment criteria

Pea Protein and Muscle Mass During Weight Loss

Obesity

A pilot study comparing the effects of pea protein versus whey protein on the preservation of muscle mass and functionality in individuals undertaking a weight loss regimen.

Completed31 enrollment criteria

Weight Loss Aid in an Exposed Population

Polybrominated Biphenyl Poisoning

This study will explore whether the use of orlistat results in weight loss that is accompanied by a reduction in the body burdens of polybrominated biphenyls (PBB) and other Persistent Organic Pollutants (POPs).

Completed18 enrollment criteria

FitLink: Improving Weight Loss Maintenance by Using Digital Data to Provide Support and Accountability...

ObesityOverweight2 more

Most adults in the U.S. are overweight or obese and find maintenance of weight loss difficult. This study is designed to aid in the development of a lifestyle modification program that can facilitate weight loss maintenance, without requiring long-term visits to a clinic for maintenance treatment.

Completed14 enrollment criteria

The Role of High Intensity Interval Training in the Treatment of Adolescent Obesity

Pediatric ObesityAdolescent Obesity1 more

The study will compare the effects of High Intensity Interval Training (HIIT) with Moderate Intensity Continuous Training (CMIT) as part of a lifestyle intervention program on BMI change in adolescents age 12-16 with obesity.

Completed15 enrollment criteria

Study of Time-restricted Eating on Weight Loss.

ObesityInsulin Resistance

This is a randomized controlled trial studying the effects of time-restricted eating (TRE) on weight loss in obese humans. Obesity is the number one risk factor for type 2 Diabetes Mellitus (T2DM), and numerous studies demonstrate that weight loss is an effective strategy to prevent T2DM and improve the metabolic health of people diagnosed with T2DM. Unfortunately, classical calorie restriction diets often fail to produce long-term weight loss due to low compliance, reduced resting metabolic rate (RMR), and other factors. Therefore, novel dieting techniques must be explored in order to successfully treat obesity and prevent T2DM. Studies in mice provide compelling evidence that feeding/fasting cycles can be altered to produce beneficial effects on weight loss and metabolic health markers in the absence of calorie restriction. Limited research in human subjects suggests that this feeding paradigm may translate to human health as well, however, more research needs to be done in order to confirm this hypothesis. This study will determine if TRE can lead to weight loss in obese human subjects. Secondary outcomes include changes in body composition, HOMA-IR, hormonal and biochemical serum markers, RMR, and total energy expenditure (TEE).

Completed21 enrollment criteria

Peer Support for Weight Loss Maintenance

Obesity

The primary aim of this study is to test the efficacy of patient-provided treatment for weight-loss maintenance.

Completed10 enrollment criteria

Effect of a Three Combined Probiotics Supplementation on Weight Loss in Obese/Overweight Children...

ObesityChildhood

This program is a double-blind, randomized, placebo-controlled study. Investigators expect to enroll 100 overweight or obese children those ages 6 to 18 years. A product that containing three probiotics will be prescribed for study group for 12 weeks plus diet and exercise guidance, while the control group will be given a placebo plus diet and exercise guidance.

Completed6 enrollment criteria
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