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Overweight clinical trials

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NCT ID: NCT03068221 Completed - Overweight Clinical Trials

Clinical Sciences Research Proposal- The Effect of Physical Exercise on PCOS Overweight Female Adolescents

Start date: March 15, 2017
Phase: N/A
Study type: Interventional

The Poly Cystic Ovary Syndrome (PCOS), is one of the most common reasons for subfertility, oligomenorrhea and amenorrhea. With the occurrence of 6-20% of the general adult women population. One of the main criteria of this syndrome is a hyper androgenic state. More than 50% of women who have PCOS are overweight. In the teenage population, PCOS is common in 5-10% of teenage girls. A recent research has shown that elite athlete teenage girls have higher serum androgen levels, especially in anaerobic types of sport. The purpose of this experiment is to examine the reaction of teenage PCOS overweight girls towards anaerobic exercise. To determine if their hyperandrogenic state is more adapted to excel in anaerobic exercise compared to teenage overweight girls without PCOS.

NCT ID: NCT03066882 Completed - Obesity Clinical Trials

Dietary Effects on Weight Loss and Lipid Profile in Sedentary Women

Start date: May 10, 2012
Phase: N/A
Study type: Interventional

Negative-calorie diet is among the popular dieting guides for weight loss; however, there is still little knowledge about this method. The present study aimed to determine the effects of negative-calorie diet on weight loss and lipid profile, and to compare its efficiency with low-calorie diet.

NCT ID: NCT03062163 Completed - Lipolysis Clinical Trials

Efficacy and Safety of Resveratrol and Lipoic Acid Transdermal Patch for Lipolysis in Overweight Volunteers

Start date: January 23, 2017
Phase: N/A
Study type: Interventional

To evaluate the lipolysis effect of resveratrol and lipoic acid transdermal patch in overweight volunteers

NCT ID: NCT03060525 Completed - Obesity Clinical Trials

Deaf Weight Wise 2.0: A Healthy Lifestyle Intervention With Deaf Adults Who Are Overweight or Obese

DWW2
Start date: December 2016
Phase: N/A
Study type: Interventional

The purpose of the Deaf Weight Wise 2.0 (DWW 2.0) study is to test an evidence-based, comprehensive program to modify obesity-related health behaviors with Deaf people ages 21 to 70 who use American Sign Language (ASL) as their primary language. Participants will be randomized to one of four arms: immediate intervention vs. intervention delayed one year, and in-person group intervention vs. individual intervention delivered via videophone. The investigators' primary hypothesis is that participants in the immediate DWW 2.0 intervention will increase their physical activity and reduce their caloric intake and body weight compared with those in the delayed intervention group (no intervention yet).

NCT ID: NCT03059472 Completed - Obesity Clinical Trials

Strong Hearts for New York: A Rural Heart Disease Prevention Study

Start date: March 31, 2017
Phase: N/A
Study type: Interventional

Strong Hearts for New York is a research study which aims to reduce cardiovascular disease (CVD), improve quality of life, and reduce CVD related health care costs in rural communities. Our aim is to better understand how changes in lifestyle can affect the health of rural women and others in their communities.

NCT ID: NCT03058367 Completed - Obesity Clinical Trials

Benefit and Tolerability of IQP-AE-103 in Weight Loss

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

This study is to evaluate the benefit and tolerability of two dosages of IQP-AE-103 (990mg and 1980mg daily) in reducing body weight in overweight and moderately obese subjects

NCT ID: NCT03057873 Completed - Overweight Clinical Trials

The Effect of a High Protein, High Fiber Dietary Supplement on Weight and Fat Loss

Start date: February 13, 2017
Phase: N/A
Study type: Interventional

The objective of this study is to investigate the effect of a high protein, high fiber dietary supplement on weight and fat loss in healthy overweight adults. Half of participants will receive a high protein, high fiber supplement twice a day for 12 weeks, and half of the subjects will receive a placebo (that contains the same amount of calories as the supplement) twice a day for 12 weeks.

NCT ID: NCT03055416 Completed - Clinical trials for Overweight and Obesity

Mobile Phone Intervention for Physical Activity Maintenance in African American Men (MobileMen)

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

African American men are at risk of developing chronic disease partly due to low levels of regular physical activity. Studies have been effective in increasing physical activity levels in African American men; however for the health benefits of exercise to be maintained continued physical activity is necessary. The purpose of the current study is to develop a mobile phone application for African American men that will help them maintain their physical activity levels.

NCT ID: NCT03042208 Completed - Clinical trials for Overweight and Obesity

Weight Watchers and Families

Start date: January 2, 2015
Phase: N/A
Study type: Interventional

Research suggests that when one spouse loses weight, the other spouse does too. This study will examine whether a ripple effect is observed in untreated spouses and children of individuals participating in a nationally available weight loss program. Participants will be randomly assigned to either receive Weight Watchers immediately or at the end of a 6-month waiting period. Participants and untreated spouses (and any children in the home) will be assessed at baseline, 3, and 6 months.

NCT ID: NCT03041142 Completed - Clinical trials for Cardiovascular Risk Factor

Program of Physical, Nutritional and Psychological Activities With Overweight Schoolchildren

PANPES
Start date: October 1, 2015
Phase: N/A
Study type: Interventional

Obesity has been considered as one of the primary factors for the development of pathologies and cardiovascular risk factors. In the child it has been mediator for the development of these comorbidities still in childhood, in the adolescence and more strongly in the adult age, at the time of most cardiovascular events with death records. Objective: To analyze the effects of an interdisciplinary intervention program on the cardiovascular risk factors of overweight and obese children. Methods: It was conducted a physical activity program, nutritional and psychological orientations, lasting ten weeks with overweighed children and their mothers. Thirty-three children with BMI considered overweight and obese participated in the study, they were divided into two groups, experimental (n=14) and control (n=19). Physical activities occurred 3 times a week with children and once a week with mothers. Nutritional and psychological counseling occurred once a week with both children and mothers. BMI, waist circumference, waist-height ratio, percentage of fat, cardiorespiratory fitness, systolic and diastolic blood pressure, lipid profile, glucose, left ventricular mass, daily energy intake and parental perception of children's weight were analyzed. For the statistical analysis it was first verified the normality of the data by the Shappiro Wilk test, with the variables that presented normality the possible differences were verified through the Anova test of mixed design with the post hoc of Bonferroni, for the normal variables, but that presented significant difference in the initial moment of the research, it was resorted to the Ancova, finally, for the non-normal variables the "U" tests of Mann Whitney and Wilcoxon.