Obese Clinical Trial - Influence of Changes in Food Group Variety on Food

Status Active, not recruiting

Clinical Trial Summary

The purpose of this study is to find out if there is any change in diet on food cravings and weight loss in the 12 months following bariatric surgery.

Clinical Trial Description

Research suggests that satiation processes in obese patients may be impaired, possibly resulting in excessive energy intake and poorer weight loss outcomes. One factor that may contribute to disruption of satiation processes and related overconsumption is dietary variety. Additionally, food cravings for restricted foods are believed to contribute to poor compliance to diets, and in controlled feeding studies, food cravings are the most frequently provided reason for poor dietary adherence. Interestingly, several investigations have found that cravings decrease when individuals follow a very-low-calorie or monotonous diet (9-11). Thus, reductions in the variety of the diet may also reduce food cravings, and assist in dietary adherence. It is also possible that the type of surgical procedure performed may influence changes in dietary variety, and consequently food cravings. To date, few studies have analyzed bariatric surgery patients' selection of foods within specific food groups and no study has examined the variety of foods consumed within food groups. Changes in food group variety which facilitate improvements in regulation of energy intake and body weight among obese individuals after behavioral weight loss may have a similar impact in patients who undergo bariatric surgery. Additionally, no studies have examined the relationship between changes in dietary variety and food cravings, and how these factors may be related to weight loss outcomes in any population. Primary Objectives: To examine by surgery type(Roux-En-Y gastric bypass [RYGB], laparoscopic adjustable gastric banding [LAGB], vertical sleeve gastrectomy [VSG]) 1. changes in dietary variety from pre- to post-bariatric surgery at 3, 6, and 12-months 2. changes in variety of high-energy-dense foods and changes in cravings of high-energy-dense foods at 3, 6, and 12 months and 3. changes in variety of high-energy-dense and low-energy-dense foods and changes in energy intake and weight loss at 3, 6, and 12 months. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01399177
Study type	Observational
Source	The University of Tennessee, Knoxville
Contact
Status	Active, not recruiting
Phase
Start date	June 2011
Completion date	December 31, 2024

View Details

See also
Status	Clinical Trial	Phase
Completed	`NCT04105075` - COPD in Obese Patients
Completed	`NCT04099654` - The Effect of Core Stabilization Exercise Program in Obese Subjects Awaiting Bariatric Surgery	N/A
Recruiting	`NCT05857150` - Exercise Response in Humans With Obesity
Completed	`NCT03532672` - Early Effect of Fasting on Metabolic, Inflammatory, and Behavioral Responses in Females With and Without Obesity	N/A
Completed	`NCT02086448` - Sleep Disordered Breathing, Obesity and Pregnancy Study (SOAP)	N/A
Completed	`NCT02618486` - The Effects of Obesity on Non Surgical Periodontal Therapy	N/A
Completed	`NCT01724502` - Mitochondrial Dysfunction in Diabetes	N/A
Completed	`NCT01724515` - PGC-1 and Mitochondrial Dysfunction in Diabetes	N/A
Active, not recruiting	`NCT01634204` - Efficacy of a Web-based Weight Loss Program	Phase 2
Completed	`NCT01479933` - Glucose Metabolism Effects of Vitamin D Supplementation in Prediabetes	N/A
Completed	`NCT01421589` - Growth Hormone Treatment on Phosphocreatine Recovery in Obesity	N/A
Completed	`NCT03528304` - Native Women's Wellness: Contingency Management for Tobacco Cessation and Weight Loss	N/A
Completed	`NCT01467817` - Obesity/Overweight in Persons With Early and Chronic Spinal Cord Injury (SCI)	N/A
Completed	`NCT01726647` - Metabolism Associated With Abdominal Fat Mass Distribution	N/A
Active, not recruiting	`NCT02125149` - The Expecting Study	N/A
Completed	`NCT05737927` - Pharmacodynamics and Pharmacokinetics of Different Glucose Bead Formulations in Obese Healthy Subjects	Phase 1
Completed	`NCT05433506` - Safety and Pharmacokinetics of HU6	Phase 1
Completed	`NCT02871882` - Ox Bile- Conjugated Bile Acids Sodium in Type II Diabetes Mellitus	Phase 2
Completed	`NCT03298464` - Study of NGM313 in Obese Participants	Phase 1
Completed	`NCT05061173` - Comparison of Aerobic, Resistance, and Combined Training in Overweight/Obese Hypertensive Adults	N/A

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

Influence of Changes in Food Group Variety on Food Cravings, Energy Intake, and Weight Loss After Bariatric Surgery

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms