Discovering Determinants of Food Intake by Application of Artificial Intelligence to Complex, High-Dimensional Data

StatusNot Yet Recruiting
PhaseNot specified
Started

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Record History

The 50 most recent of 85 record versions are listed below. See every version on ClinicalTrials.gov ↗

  1. Minor Start date: Oct 27, 2026 to Oct 28, 2026
  2. Minor Start date: Oct 26, 2026 to Oct 27, 2026
  3. Minor Start date: Oct 25, 2026 to Oct 26, 2026
  4. Minor Start date: Oct 22, 2026 to Oct 25, 2026
  5. Minor Start date: Oct 21, 2026 to Oct 22, 2026
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  1. Minor Start date: Oct 20, 2026 to Oct 21, 2026
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  26. Minor Start date: Aug 31, 2026 to Sep 1, 2026v55
  27. Minor Start date: Aug 30, 2026 to Aug 31, 2026v54
  28. Minor Start date: Aug 27, 2026 to Aug 30, 2026v53
  29. Minor Start date: Aug 26, 2026 to Aug 27, 2026v52
  30. Minor Start date: Aug 25, 2026 to Aug 26, 2026v51
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  34. Minor Start date: Aug 19, 2026 to Aug 20, 2026v47
  35. Minor Start date: Aug 18, 2026 to Aug 19, 2026v46
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  39. Minor Start date: Aug 12, 2026 to Aug 13, 2026v42
  40. Minor Start date: Aug 11, 2026 to Aug 12, 2026v41
  41. Minor Start date: Aug 10, 2026 to Aug 11, 2026v40
  42. Minor Start date: Aug 7, 2026 to Aug 10, 2026v39
  43. Minor Start date: Aug 6, 2026 to Aug 7, 2026v38
  44. Minor Start date: Aug 5, 2026 to Aug 6, 2026v37
  45. Minor Start date: Aug 4, 2026 to Aug 5, 2026v36
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Background: Many people in the United States are overweight or obese. Researchers want to learn why some people can overeat and not gain weight, whereas others who do not overeat still gain weight. Objective: To study factors related to food intake that can lead to weight gain over time. Eligibility: Healthy adults aged 18 to 60 years. Design: Participants will have 6 to 8 clinic visits over 2 years. The first 3 or 4 study visits will be 1 week apart. Procedures during visits may include the following: Collection of blood, hair, urine, and stool samples. Measurement of the waist, neck, thighs, and other parts of the body. Dual energy x-ray absorption (DXA) scan: Participants will lie still on a padded table while they are scanned to measure body fat. Physical activity monitor: Participants will wear a monitor on the wrist for 2 weeks. Cognitive tests: Participants will perform tasks to measure attention, memory, and brain function. Continuous glucose monitor. Participants will wear a device that measures their blood glucose for 1 week. Mixed meal test and stomach emptying test. Participants will drink a breakfast shake and swallow a dose of acetaminophen. Blood will be drawn over the next 4 hours. Resting metabolic rate: Participants will wear a clear hood over their head while they rest for 20 minutes. The hood will measure the gases they breathe. Breakfast and lunch test. Participants will eat a standard breakfast. They will be allowed to select from foods and eat as much as they like at lunch. They will be asked how hungry or full they are. Questionnaires. Participants will answer questions about their health, sleep, physical activity, and eating.
Trial Details
NCT Number NCT07637656
Lead Sponsor National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Conditions
(from sponsor)
Healthy Volunteer
Enrollment 800 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov