A Natural History Study of Metabolic Sizing in Health and Disease
NCT ID: NCT05398783
Last Updated: 2026-01-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
2000 participants
OBSERVATIONAL
2022-10-25
2031-07-01
Brief Summary
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Scientists have long used simple measures (such as height and weight) to estimate how much a person s body uses food (calories) as energy, as commonly called the metabolic rate. But metabolism varies among people with similar body sizes. Scientists now believe the old formulas for estimating metabolic rates may not work well for all people. Researchers want to find more accurate ways to measure a person s metabolism.
Objective:
This natural history study will examine the relationships between metabolism, body composition, and body surface area in a wide range of people.
Eligibility:
Healthy children and adults aged 2 years or older. Also, people aged 2 years or older with conditions that may alter metabolism. These may include diabetes, obesity, renal disease, or cancer.
Design:
Participants will spend 2 days and 1 night in the hospital. They will provide a medical history and answer questions about their activity levels, the foods they eat, and their lifestyle. They will also eat a special diet.
Participants will undergo many tests:
They will lie in a bed with a clear hood covering their head for 30 to 45 minutes to measure the gases in their breath.
They will lie on a padded table for about 15 minutes while their body is scanned.
They will stand on a platform while a 3D scanner measures their body.
They will have a test to measure how fast an electric signal moves through their body.
They will grip an instrument to measure the strength of their hands.
They will drink salty water and provide blood and urine samples.
Participants may be invited to return for these 2-day visits up to 8 times per year. Return visits must be at least 2 weeks apart.
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Detailed Description
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This study will examine the relationships between comprehensively measured resting energy expenditure (REE), body composition, and body surface area (BSA) in a wide range of healthy and diseased individuals.
Objectives:
Primary Objectives:
* To compare estimated and measured BSA.
* To determine if measured BSA is associated with REE independent of body composition measures
Endpoints:
Primary Endpoints:
* Mean difference and limits of agreement at baseline between measured BSA and predicted BSA calculated from traditional biometrics such as height and weight.
* Increase in R\^2 when measured BSA is added to equations predicting REE.
Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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Healthy Volunteers
Male and female volunteers aged 2+ years in good general health as evidenced by medical history
No interventions assigned to this group
Patients
Male and female patients aged 2+ years diagnosed with diseases thought to alter metabolism or body composition and/or taking medication thought to alter metabolism or body composition
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
Cohort 1 - Healthy Volunteers
* Male or female, aged \>=2 years
* In good general health as evidenced by medical history
Cohort 2 - Patients
* Male or female, aged \>=2 years
* Diagnosed with diseases thought to alter metabolism or body composition (such as weight loss or gain, diabetes, renal disease, obesity, cancer, etc.) or taking medications thought to alter metabolism or body composition.
Exclusion Criteria
* Participants over 200 kg due to the weight limit of the equipment.
* Presence of any implanted device that would interfere with measurements.
* Any moderate to severe limitations in mobility that would impede participation
* Hemoglobin less than 10 g/dL (in participants who would have blood drawn for research purposes)
* Participants with dietary allergies, intolerances or eating patterns that would preclude them from consuming metabolic meals.
* Participants unwilling or unable to give informed consent.
* Participants with any other significant physical, medical, or psychiatric limitations, illness or conditions that may preclude them from completing the majority of the tests in this study per the discretion of the PI.
2 Years
99 Years
ALL
Yes
Sponsors
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National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
NIH
Responsible Party
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Principal Investigators
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Kong Y Chen, Ph.D.
Role: PRINCIPAL_INVESTIGATOR
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Locations
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National Institutes of Health Clinical Center
Bethesda, Maryland, United States
Countries
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Central Contacts
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Facility Contacts
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For more information at the NIH Clinical Center contact Office of Patient Recruitment (OPR)
Role: primary
Related Links
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NIH Clinical Center Detailed Web Page
Other Identifiers
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000617-DK
Identifier Type: -
Identifier Source: secondary_id
10000617
Identifier Type: -
Identifier Source: org_study_id
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