Working… Menu

Physical and Behavioral Traits of Overweight and Obese Adults

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. Identifier: NCT00428987
Recruitment Status : Recruiting
First Posted : January 30, 2007
Last Update Posted : September 18, 2019
Information provided by (Responsible Party):
National Institutes of Health Clinical Center (CC) ( National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) )

Tracking Information
First Submitted Date January 27, 2007
First Posted Date January 30, 2007
Last Update Posted Date September 18, 2019
Study Start Date January 26, 2007
Primary Completion Date Not Provided
Current Primary Outcome Measures Not Provided
Original Primary Outcome Measures Not Provided
Change History Complete list of historical versions of study NCT00428987 on Archive Site
Current Secondary Outcome Measures Not Provided
Original Secondary Outcome Measures Not Provided
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
Descriptive Information
Brief Title Physical and Behavioral Traits of Overweight and Obese Adults
Official Title Study of the Phenotype of Overweight and Obese Adults
Brief Summary

This study will describe the phenotype (physical and behavioral traits) of overweight and obese people. It will characterize the hormones, metabolism, food preferences, fitness and physical activity levels, sleep patterns and thought processes in people with and without weight problems. Genetic material will be collected for studies of the internal codes that influence body weight.

People over 18 years of age from all weight categories (lean, overweight, obese) who are reasonably healthy may be eligible for this study. Participants undergo the following tests and procedures:

  • Physical exam, electrocardiogram, blood and urine tests, instructions for recording food intake for 7 days
  • Metabolic studies for menstruating women.
  • Resting metabolic rate to study how many calories the body burns at rest.
  • Mixed meal test to measure hormones such as insulin that regulate blood sugar.
  • Glucose tolerance test to determine how sensitive the body is to insulin.
  • 24-hour energy expenditure to measure the amount of oxygen breathed in and the amount of carbon dioxide breathed out.
  • Repeat 24-hour energy expenditure.
  • Diurnal blood sampling and temperature assessment to study the body s internal clock.
  • Air-displacement plethysmography (Bod Pod) to measure body composition.
  • Dual energy x-ray absortiometry (DEXA) to measure body fat and bone density.
  • Repeat Bod Pod and DEXA.
  • Anthropometric measurements and bioelectrical impedance to measure height, weight, and circumferences, skinfold thickness, fluid status and percentage body fat.
  • Bromide dilution to measure the amount of water not in cells in the body.
  • Doubly labeled water to measure the amount of calories burned in a 7-day period.
  • 24-hour diet reports.
  • Endothelial reactivity to measure how the blood vessels stretch or dilate for assessing cardiovascular health.
  • Treadmill or bicycle exercise capacity test.
  • Physical activity monitor.
  • Unicorder to detect any breathing difficulties that may interfere with sleep.
  • Fat and muscle biopsy to look for variations in gene expression in fat tissue and muscle.
  • Neurocognitive testing to check memory, decision-making, hand-eye coordination, and reasoning.
  • Evaluation of mood problems and assess personality type.
  • Evaluation to assess the quantity and quality of pain experienced.
  • Taste testing to determine the response to bitter, salty, sweet and sour substances.
  • Occupational therapy evaluation to explore the subject s adaptations, if any, for performing personal, social or professional activities; the subject s views on his or her weight, body size and shape, and strategies to control weight.
Detailed Description

Although complex metabolic, hormonal, and neural networks operate to control body weight, obesity is in most cases, the result of over-feeding and inactivity.

In the majority of obese patients, patterns of fundamental behavior determine the success or failure of weight loss interventions. Behavior is controlled to some degree by conscious decision making and is influenced by signals from the integrated networks involved in body weight regulation. The contributions of behavior, environment, socioeconomic status, physiology and genetics assure that no single therapeutic regimen will be successful in all obese individuals. In order to explore the factors that impede weight loss and result in weight regain, the obese phenotype and its variants must be defined. The purpose of this study is to detail hormonal, metabolic, cognitive and behavioral traits across the spectrum of weight categories utilizing the state-of the-art facilities of the Metabolic Units at the Mark O. Hatfield Clinical Research Center, NIH. Genetic material will be banked for analysis of phenotypic subgroups as they emerge.

Patients over the age of 18 are eligible for this study. While childhood obesity is an important public health issue, the variables of growth and hormonal controls will be delineated in separate studies. Over-weight and obese patients are encouraged to participate in as full an evaluation as feasible. Lean individuals will be recruited to create a normative database for body composition (dual energy x-ray absortiometry, air displacement plethysmography), energy expenditure (resting energy expenditure, 24h respiratory chamber and doubly labeled water) and other techniques used to study traits of importance. The study will be conducted in both the inpatient and outpatient setting and can include evaluation of hormones, diurnal variation, sleep, eating behavior and taste perception, physical fitness, psychological and neurocognitive functioning. Importantly, this protocol is the means by which pilot data are obtained to develop novel approaches and hypotheses for studying obesity and its associated traits.

Study Type Observational
Study Design Observational Model: Cohort
Time Perspective: Prospective
Target Follow-Up Duration Not Provided
Biospecimen Not Provided
Sampling Method Not Provided
Study Population Not Provided
  • Morbid Obesity
  • Healthy Volunteers
Intervention Not Provided
Study Groups/Cohorts Not Provided
Publications *

*   Includes publications given by the data provider as well as publications identified by Identifier (NCT Number) in Medline.
Recruitment Information
Recruitment Status Recruiting
Estimated Enrollment
 (submitted: June¬†3,¬†2015)
Original Enrollment Not Provided
Study Completion Date Not Provided
Primary Completion Date Not Provided
Eligibility Criteria

Obese subjects:

  1. Obese men and women over the age of 18 years;
  2. BMI greater than 30;

Overweight subjects:

  1. Overweight men and women over the age of 18 years;
  2. BMI greater than 25 and less than 30

Control subjects (may be matched for age, sex and years of education):

  1. Normal weight men and women over the age of 18 years;
  2. BMI greater than 18.5 and less than 25


  1. Patients with significant physical limitations that may preclude them from completing the majority of the tests in this study.
  2. Current, unstable medical conditions including cardiac ischemia; severe respiratory insufficiency requiring oxygen therapy; hepatic or cardiac failure as assessed by history and physical exam;
  3. Any psychiatric condition that would preclude participation in the study;
  4. Patients unwilling or unable to give informed consent.

Additional exclusion for lean control subjects:

  1. Previous history of obesity as an adolescent or adult;
  2. Current or past history of eating disorders such as anorexia nervosa or bulimia.

Exclusions for both cannabis users and controls:

  1. Dependence on drugs other than nicotine, caffeine and cannabis, within the past 6 months
  2. Any history of intravenous illegal drug use
  3. Alcohol use of more than 5 drinks per day, on 3 or more days in a week; or more than 15 drinks per week
  4. History of hepatitis B or C or current hepatitis A, B or C, or other liver disease associated with steatosis
  5. HIV
  6. History of diabetes (type 1 or type 2) or polycystic ovary disease or other conditions that may confound our study results
  7. Professional or collegiate athletes or participation in more than 60 minutes per day of vigorous exercise
  8. Use of prescribed or over the counter or herbal/alternative medications/ preparations with effects on glucose and lipid metabolism other than oral contraceptives
  9. Pregnancy or lactation
  10. Any condition or physical attribute which would interfere with MRI study e.g. claustrophobia, cochlear implant, metal fragments in the eye, certain types of tattoos or other metal implanted in the body
Sexes Eligible for Study: All
Ages 18 Years and older   (Adult, Older Adult)
Accepts Healthy Volunteers Yes
Contact: Antoinette C Rabel, C.R.N.P. (301) 451-8893
Contact: Ranganath Muniyappa, M.D. (301) 451-7702
Listed Location Countries United States
Removed Location Countries  
Administrative Information
NCT Number NCT00428987
Other Study ID Numbers 070077
Has Data Monitoring Committee Not Provided
U.S. FDA-regulated Product Not Provided
IPD Sharing Statement Not Provided
Responsible Party National Institutes of Health Clinical Center (CC) ( National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) )
Study Sponsor National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Collaborators Not Provided
Principal Investigator: Ranganath Muniyappa, M.D. National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
PRS Account National Institutes of Health Clinical Center (CC)
Verification Date February 25, 2019