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Weight Gain clinical trials

View clinical trials related to Weight Gain.

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NCT ID: NCT04180878 Completed - Pregnancy Clinical Trials

Promoting Appropriate Weight Gain Pregnant Women

GRUVE
Start date: June 26, 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to learn if engaging in group based phone counseling (GBPC) and an interactive physical activity monitoring system can help pregnant women gain an appropriate amount of weight during pregnancy.

NCT ID: NCT04174521 Completed - Obesity, Childhood Clinical Trials

Association Between Mother and Child Weight Gain: Statistical Methods With Validation

Start date: June 26, 2019
Phase:
Study type: Observational

Using retrospective data from the Vanderbilt University Medical Center electronic health record, the investigators will study the association between mother's weight / weight change before and during pregnancy and the development of childhood obesity up until 5 years of age.

NCT ID: NCT04173559 Not yet recruiting - Pregnancy Related Clinical Trials

Sleep and Tracking Effects in Pregnancy Study

STEP
Start date: May 2023
Phase: N/A
Study type: Interventional

Purpose: The investigators hypothesize that a simple, personalized, smartphone-based activity intervention using a wrist-based activity tracker will help high risk pregnant women reduce their stress during pregnancy. Participants: Pregnant women enrolled in prenatal care at the University of North Carolina who have a documented moderate or high level of perceived stress ( ≥ 14) and are at high risk for adverse pregnancy outcomes due to body mass index of ≥ 30 kg/m2 or history of gestational hypertension, preeclampsia, intrauterine growth restriction, or preterm birth <37 weeks' in a prior pregnancy. Procedures: Women meeting inclusion criteria will be recruited through the University of North Carolina prenatal care clinics. They will be contacted for possible participation at regularly scheduled prenatal visits and/or ultrasound. They may also be contacted for possible participation by remote methods (e.g., Telehealth). Women who are enrolled will complete validated dietary, stress, sleep, and body image questionnaires. Enrolled women will then be randomized to receive standard obstetrical care or enhanced counseling. All participants will receive a wrist-based activity tracker. Maternal blood sample for biochemical markers of stress and gene expression will be obtained at the initial visit; a followup blood sample will be obtained later in pregnancy, and a small portion of the placenta saved at delivery. Maternal and neonatal outcomes will be compared between groups.

NCT ID: NCT04168749 Enrolling by invitation - Weight Gain Clinical Trials

Efficacy and Safety of Industrially Prepared 3 Chamber Bag Parenteral Nutrition for Premature Infant

ESIP3CB
Start date: November 15, 2019
Phase:
Study type: Observational

This study was designed to evaluate whether industrially prepared standardizing total parenteral nutrition is at least non-inferior to compounded TPN and provides nutritional intakes according to the new guidelines and provides the expected weight gain in preterm babies with a birth weight between 1250 and 2000g admitted in our NICU between 2015 & 2018

NCT ID: NCT04145427 Recruiting - Weight Gain Clinical Trials

Impact of a LCD on Metabolic Inflexibility and Cardiovascular Risk in Liver Transplant Patients

Start date: February 27, 2020
Phase: N/A
Study type: Interventional

This study is looking to see how a 6-month low carbohydrate diet can affect the body's ability to use energy in addition to the affects it has on the heart and blood vessel health.

NCT ID: NCT04142216 Completed - Hemodialysis Clinical Trials

Effect of Chewing Gum in Hemodialysis Patients

Start date: October 14, 2019
Phase: N/A
Study type: Interventional

The aim of this prospective randomized controlled study was to investigate the effects of chewing gum on interdialytic weight gain, thirst, dry mouth and intradialytic symptoms in hemodialysis patients.

NCT ID: NCT04140968 Terminated - Menopause Clinical Trials

Progesterone and Resting Energy Expenditure

P4&REE
Start date: November 1, 2019
Phase: Phase 4
Study type: Interventional

This study evaluates the effect of micronized progesterone substitution in the luteal phase on resting energy expenditure in women during menopausal transition.

NCT ID: NCT04135729 Completed - Weight Loss Clinical Trials

Mental Health in Fitness Instructors

Start date: November 1, 2019
Phase:
Study type: Observational

The aim of this project is to improve the evidence-base regarding lifestyle and mental health symptoms among fitness instructors. A national cohort of fitness instructors will be invited to participate in this study by responding to an online questionnaire. The questionnaire will consist of items regarding exercise, nutrition, eating disorders, the menstrual cycle, depression, anxiety, body dissatisfaction and satisfaction, drive for muscularity and leanness, and experiences of sexual harassment. Findings from this study will provide an evidence-base for initiatives to improve/optimize mental health among fitness instructors, and also in the process of developing fitness centres to a core partner in public health and health promotion work.

NCT ID: NCT04131023 Completed - Clinical trials for Gestational Weight Gain

Metabolic Tracking and Weight Gain During Pregnancy

Start date: September 17, 2017
Phase: N/A
Study type: Interventional

In this study, the investigators aimed to have pregnant women use a hand-held device to track increases in daily caloric needs during pregnancy. Weight gain was assessed over time with the goal of reducing excessive gestational weight gain relative to a group of pregnant women who received standard prenatal care.

NCT ID: NCT04130386 Completed - Clinical trials for Motivational Interviewing

Motivational Interviewing to Address Freshman Weight Gain

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

The purpose of the study is to determine the effect of Motivational Interviewing and e-health education on body composition and psychological outcomes. After baseline testing, participants will be randomly assigned to a motivational interviewing or e-health education group for a 10-week intervention. Variables of interest include: body composition, physical activity, food consumption and self-determination theory constructs.