Your search for "Nutrition and Metabolism" found 26 matches:
ARROW study: Weight loss study

Research study looking at your body's response to dietary changes after completing a free weight loss program....

Protocol #: 18-0091

Solid foods and infant growth

Your baby may be eligible if they are: - Exclusively breastfed - Younger than six months of age - Full term (> 37-weeks’ gestation) - Have not yet been introduced to solid foods This is a 7-month long study, with visits occurring once every month. The first visit, 9-month visit, an...

Protocol #: 19-0546

Blueberry intake and infant gut health

Your breastfed baby may be eligible if they are: - Younger than six months of age - Exclusively breastfed - Full term (> 37-weeks’ gestation) - Have not yet been introduced to solid foods This is a 7-month long study, with visits occurring once every other month. The first and last ...

Protocol #: 20-1659

Early iron exposure on the gut microbiota in young infants

This is a four month-long study, beginning at birth. The first study visit is conducted at the University of Colorado Hospital and the last visit takes place at Children’s Hospital Colorado. The other four visits are conducted in your home. Formula is provided to all study participants for...

Protocol #: 18-1317

Does When You Exercise Matter? A Randomized Trial Comparing the Effect of Morning versus Evening Aerobic Exercise on Weight Loss and Compensatory Behaviors

If you join the study, you will undergo screening evaluations to see if you are eligible to be in the study. If you are eligible to be in the study, you will be randomized to one of two study groups. Which group you are assigned to will be chosen by chance by a procedure similar to the t...

Protocol #: 21-3094

REACH - Role of microvascular insulin resistance and cardiorespiratory fitness in diabetes

Participants will undergo baseline testing of heart and blood vessel function as well as skeletal muscle function and exercise ability. Participants will then do cardiovascular exercise for 15 weeks, and all testing will be repeated....

Protocol #: 20-2723

The short-chain fatty acid acetate for improving age-associated arterial dysfunction

Specific Aim: To determine the following before and after 12 weeks of oral supplementation with calcium acetate vs. placebo (calcium citrate) in healthy men and women 50+ years of age: a) Endothelium-dependent dilation, assessed as brachial artery flow-mediated dilation (FMDBA) [primary o...

Protocol #: 22-0473

BURST2D Study: Breaking up sedentary time to improve glucose control in a population at risk for developing type 2 diabetes

The purpose of the study is to compare two different physical activity interventions (BREAK or ONE) to learn about their effects on blood sugar and metabolism. Participants will be randomized to one of two interventions: ONE (45-minutes of brisk walking at least 5 days per week) and BREAK ...

Protocol #: 20-1900

Time2Eat Weight Loss Study- Join this CU Anschutz weight loss research study for adults age 18-65. Receive a free 12 month diet and exercise program.

Join this CU Anschutz weight loss research study for adults age 18-65. Receive a free 12 month diet and exercise program....

Protocol #: 22-1829

Locations: UCD Anschutz Health & Wellness Center

uHoWL Research Study

Are you interested in a research study on women's reproductive hormones? We are conducting a study among women aged 18-40 who have regular menstrual cycles, are not using hormonal birth control, and have a body mass index between 27-45. ...

Protocol #: 21-3957

Neuronal and behavioral effects of an implicit priming approach to improve eating behaviors in obesity

What is involved: -A 12-week intervention involving viewing food or food images (study visits once per week) -Study days before and after the intervention to measure brain responses to food images -Measures of body composition, mood, physical activity, and eating behaviors St...

Protocol #: 20-2821

The Bone, Exercise, Alendronate, and Caloric Restriction (BEACON) Trial

Protocol #: 22-2041

Integrated Lifestyle Intervention to Promote Weight Loss Study (COMIRB 23-1154)

If you join the study, you will undergo 2-3 screening visits to see if you are eligible to be in the study. If you are eligible to be in the study, you will receive a 6-month integrated lifestyle intervention program. This integrated program includes PreventT2 (formally known as the Diabet...

Protocol #: 23-1154

BfedBwell cancer survivorship nutrition program: proof-of-concept pilot study

Cancer survivors who have completed active treatment within the last five years and who have BMI 25-45 kg/m2 will take part in a 12-week study of the BfedBwell survivorship nutrition program. BfedBwell includes group nutrition education and discussion, skills development sessions and cooki...

Protocol #: 23-1501

Location: Colorado Research Center, CTRC-adult, CU Anschutz non-hospital research facilities

Effect of weight loss on intermuscular adipose tissue (IMAT) signaling

Following screening visits involving body composition measures, blood testing, strength testing, and a thigh muscle biopsy, participants will go through a 12-week dietary intervention for weight loss. After 12 weeks, this will be followed by the same testing and biopsies that were complete...

Protocol #: 23-0545

Effects of early as compared to late time restricted eating on weight loss and metabolic outcomes in adults with obesity

Protocol #: 22-1829

Location: Anschutz Health and Wellness, Outpatient CTRC

Feasibility and Preliminary Efficacy of a Reverse Diet as a Novel Weight Loss Maintenance Strategy for Weight-Reduced Adults with Overweight/Obesity

In this study, we will be evaluating the effects of a reverse-diet compared to standard weight loss maintenance advice....

Protocol #: 17-1726

Location: Outpatient CTRC, Outpatient CTRC, University of Colorado Hospital

The Neural Underpinnings of Disinhibited Eating Behavior in Adolescents with and without Obesity

Protocol #: 19-1171

Location: Brain Imaging Center - BIC, Outpatient CTRC, Outpatient CTRC, University of Colorado Hospital

Adjunctive Anti-Obesity Pharmacotherapy in Adolescents and Young Adults after Bariatric Surgery: A Randomized Controlled Pilot Study

Protocol #: 18-2793

Location: Childrens Hospital Colorado, Outpatient CTRC, Outpatient CTRC, University of Colorado Hospital

Surgical or Medical Treatment for Pediatric Type 2 Diabetes

Surgical or Medical Treatment for Pediatric Type 2 Diabetes (STOMP-T2D) is a prospective, open-label, controlled clinical trial funded by the National Institutes of Health for a period of 5 years. We propose to study 90 participants who are 13-19 years of age and have type 2 diabetes (T2D)...

Protocol #: 19-1978

Location: Childrens Hospital Colorado, University of Colorado Hospital

Grow Up Formula Versus Nutritional Supplements: Effects on Catch Up Growth, Micronutrients Status and Solid Foods Intake in Toddlers with Mild Malnutrition

Protocol #: 20-3082

Location: Childrens Hospital Colorado

Mindfulness-Based Intervention for Depression and Insulin Resistance in Adolescents

Protocol #: 20-2649

Location: Children's Hospital National (CHN), Children's Hospital National (CHN), Childrens Hospital Colorado, Colorado State University, Uniformed Services University of Health Sciences (USUHS), Uniformed Services University of Health Sciences (USUHS)

Harnessing Cells from Human Milk; Linking Lactation to Metabolism

In this study: - Participants will complete 2 study visits (in late pregnancy & 2 wks postpartum) - Participants will have their milk production measured and provide blood and breastmilk samples If you join the study, you will be part of the study for up to a month and a half, lasting...

Protocol #: 21-2835

Location: CTRC Inpatient, Outpatient CTRC, Outpatient CTRC, University of Colorado Hospital

A single and repeat dosing study of the safety, drug exposure, and clinical activity of R-3750 in patients with mild to moderate ulcerative colitis

A single and repeat dosing study of the safety, drug exposure, and clinical activity of R-3750 in patients with mild to moderate ulcerative colitis...

Protocol #: 23-0025

Location: Outpatient CTRC, University of Colorado Hospital

Boomerang Early Feasibility Study: Prospective, multi-center, single-arm early feasibility study (EFS)

Researchers in the BOOM-IBD Clinical Trial are studying whether nerve stimulation can be effective in treating patients with Crohn's disease and ulcerative colitis....

Protocol #: 23-0063

Location: Outpatient CTRC, University of Colorado Hospital

Efficacy and safety of cagrilintide 2.4 mg s.c. in combination with semaglutide 2.4 mg s.c. (CagriSema s.c. 2.4 mg/2.4 mg) once-weekly compared to tirzepatide 15 mg s.c. once-weekly in participants with obesity

Subjects will be randomly assigned to study medication and receive dietary counseling and be followed over 78 weeks....

Protocol #: 23-1695

Location: Anschutz Health and Wellness, Outpatient CTRC