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Body Weight clinical trials

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NCT ID: NCT03945214 Completed - Stress Clinical Trials

The Impact of 8 Weeks of Digital Meditation Application and Healthy Eating Program on Work Stress and Health Outcomes

SFUC+Health
Start date: February 14, 2019
Phase: N/A
Study type: Interventional

The aim of the present study is to test the effects of a digital meditation intervention and/or a healthy eating intervention in a sample of UCSF employees with overweight and obesity (BMI>=25kg/m2) who report mild to moderate stress. We will randomize UCSF employees to 8-weeks of a digital meditation intervention (using the commercially available application, Headspace), a healthy eating intervention, a digital meditation+healthy eating intervention, or a waitlist control condition.

NCT ID: NCT03936699 Completed - Weight Loss Clinical Trials

ELIRA 2: Safety and Effectiveness of TENS Assisted Weight Loss and Appetite Suppression

ELIRA_2
Start date: June 22, 2018
Phase: N/A
Study type: Interventional

The objectives of this study are to demonstrate safety and effectiveness of a wearable patch TENS system (Appendix 2) in driving weight loss and appetite suppression when coupled with an integrated weight loss reduction strategy. The study is designed to demonstrate that TENS stimulation sufficient to drive weight loss and appetite suppression is safe and tolerable when compared to standard of care, and that adverse events/adverse device effects are similar to other TENS device use cases.

NCT ID: NCT03928483 Completed - Obesity Clinical Trials

Evaluation of a Commercial Program on Weight Loss and Health Outcomes

Start date: March 18, 2019
Phase: Early Phase 1
Study type: Interventional

To examine weight loss and acceptability of a modified WW program. This study is designed to detect differences in weight loss at the end of 24 weeks of intervention.

NCT ID: NCT03926806 Completed - Clinical trials for Type 2 Diabetes Mellitus

Yoghurt Consumption, Body Weight Management and Glycemic Control of T2DM Patients

Start date: November 25, 2016
Phase: N/A
Study type: Interventional

The study investigates the effects of consumption of yoghurt enriched with vitamins B compared to plain yoghurt, on body weight management and glycemic control of overweight/obese T2DM patients. It also investigates the effect of plain yoghurt consumption on gut hormones response of T2DM patients.

NCT ID: NCT03920787 Recruiting - Insulin Resistance Clinical Trials

Evaluating the Effect of Inositol Supplementation in Overweight Children on Basal Insulin and Body Weight

Start date: March 10, 2018
Phase: N/A
Study type: Interventional

Inositol in involved in the insulin pathway. In literature it has been demonstrated to improve insulin sensitivity and ovarian function in women affected by PCOS. In a preliminary study conducted on obese children between 7 and 15 years, the investigators have demonstrated that Inositol administration (Myo-inositol 1100 mg + D-Chiro-inositol 27,6 mg + Folic Acid 400 μg) before a Glucose Oral Tolerance Test reduces the increase of insulin levels, particularly in subjects with basal insulin ≥ 15 uU/ml. So the aim of this study is to evaluate the potential therapeutic effect of inositol, as non-pharmacologic agent, in preventing tipe II diabetes in children.

NCT ID: NCT03917758 Recruiting - Clinical trials for Diabetes Mellitus, Type 2

Antidiuretic Function Before and During Treatment With SGLT2 Inhibitors

GliRACo1
Start date: October 10, 2018
Phase: N/A
Study type: Interventional

Subjects treated with Canagliflozin, Dapagliflozin and Empagliflozin obtained improvement on blood pressure values, body weight and cardiovascular mortality but pathophysiological explanations of these effects are not yet known.

NCT ID: NCT03916354 Recruiting - Pregnancy Clinical Trials

Maternal Gestational Weight Gain and Microbiota of Maternal and Infant

Start date: May 7, 2019
Phase:
Study type: Observational [Patient Registry]

A prospective, multicenter, observational cohort study including about 550 mother-infant pairs in Beijing will be conducted to evaluate the association between mothers' gestational weight gain and the gut microbiota of them and their infants.

NCT ID: NCT03916159 Completed - Anemia Clinical Trials

Extrauterine Placental Transfusion In Neonatal Resuscitation Of Very Low Birth Weight Infants

EXPLAIN
Start date: May 1, 2019
Phase: N/A
Study type: Interventional

To investigate the effect of extrauterine placental transfusion (EPT) compared to delayed cord clamping (DCC) on the mean hematokrit on the first day of life in very low birth weight infants (VLBW) born by caesarian section. The investigators hypothesize that EPT provides higher blood volume during neonatal transition and improves neonatal outcome of VLBW infants.

NCT ID: NCT03915392 Recruiting - Cholesteatoma Clinical Trials

Diffusion Weighted MRI Accuracy in Cholesteatoma Localization

CHOLEMRI
Start date: July 1, 2018
Phase:
Study type: Observational

Magnetic resonance imaging of the middle ear has an increasing place in the therapeutic strategy in otology and especially for cholesteatoma. It is currently performed for complicated cholesteatomas and as part of the follow-up of operated patients to detect a recurrence or a cholesteatoma residue (alternative of choice to "second look" surgery). Some people take CT and MRI fusion to improve the localization of cholesteatoma. Many studies have investigated the diagnostic capabilities of MRI but very few have demonstrate their reliability in location diagnosis. The aim of the study was to propose a topographic reading method of the MRI of the middle ear and to evaluate the performances in the localization of the cholesteatoma in order to adapt the surgical management

NCT ID: NCT03893708 Completed - Weight Gain Clinical Trials

Investigating the Feasibility and Preliminary Effects of Yoga on Excessive Gestational Weight Gain

Start date: June 12, 2018
Phase: N/A
Study type: Interventional

This study will test the feasibility (i.e., acceptability, demand) of a 12-week prenatal yoga intervention on excessive gestational weight gain (GWG) in pregnant women in the second trimester (enrolled at 12-24 weeks). Participants will be randomized into the prenatal yoga intervention or a pregnancy education (e.g., information on preparing for motherhood, labor and delivery etc.) control group. Participants in both groups will be asked to attend one 75 minute class per week. The investigators hypothesize that prenatal yoga intervention will be feasible for pregnant women. The study aims are as follows: Primary Aim: Determine the feasibility (i.e., acceptability, demand) of a 12-week prenatal yoga intervention in pregnant women. In a randomized controlled pilot study comparing prenatal yoga to a pregnancy education control condition, the investigators will assess 1) acceptability (defined as satisfaction, intent to continue use, perceived appropriateness) and 2) demand (defined as attendance/adherence). Exploratory Aim 1: Ascertain the preliminary effects of prenatal yoga on excessive GWG [i.e., weight gain exceeding Institute of Medicine (IOM) recommendations]. The investigators will compare weight change between intervention and control groups. Exploratory Aim 2: Explore the potential mediators (i.e., mindfulness, self-regulation) on the effect of prenatal yoga on excessive GWG.