[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100529081":3},{"organization":4,"armGroups":7,"interventions":15,"overallOfficials":26,"centralContacts":31,"locations":40,"responsibleParty":63,"collaborators":21,"id":65,"slug":66,"hasResults":67,"nctId":68,"briefTitle":69,"officialTitle":69,"acronym":21,"eligibilityCriteria":70,"healthyVolunteers":67,"sex":71,"minAge":72,"maxAge":73,"enrollmentInfo":74,"targetDuration":21,"studyType":77,"phases":78,"briefSummary":80,"conditions":81,"keywords":84,"overallStatus":43,"whyStopped":21,"lastUpdateSubmitDate":89,"lastUpdatePostDateStruct":90,"startDateStruct":93,"completionDateStruct":95,"leadSponsor":97,"locationsCount":98},{"fullName":5,"class":6},"National Institutes of Health Clinical Center (CC)","NIH",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Premenopausal women (lean and obese)","EXPERIMENTAL","Ages 18-50 yearsBMI 18.0-24.5 mg\u002Fk\\^2 or BMI \\> 30 mg\u002Fk\\^2",[13,14],"Behavioral: Early Time-Restricted Eating","Behavioral: Conventional dietary regimen (12-hr, 9:30a-9:30p)",[16,22],{"type":17,"name":18,"description":19,"armGroupLabels":20,"otherNames":21},"BEHAVIORAL","Early Time-Restricted Eating","Participants will be provided all meals to consume within a 6-hour timeframe (9:30-3:30p)",[9],null,{"type":17,"name":23,"description":24,"armGroupLabels":25,"otherNames":21},"Conventional dietary regimen (12-hr, 9:30a-9:30p)","Participants will be provided all meals to consume within a 12-hour timeframe (9:30a-9:30p)",[9],[27],{"name":28,"affiliation":29,"role":30},"Stephanie T Chung, M.D.","National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)","PRINCIPAL_INVESTIGATOR",[32,37],{"name":33,"role":34,"phone":35,"phoneExt":21,"email":36},"Lilian S Mabundo","CONTACT","(240) 383-9379","lilian.mabundo@nih.gov",{"name":28,"role":34,"phone":38,"phoneExt":21,"email":39},"(240) 479-8137","stephanie.chung@nih.gov",[41],{"facility":42,"status":43,"city":44,"state":45,"zip":46,"country":47,"countryCode":48,"cosmosGeoPoint":49,"geoPoint":54,"contacts":55},"National Institutes of Health Clinical Center","RECRUITING","Bethesda","Maryland","20892","United States","US",{"type":50,"coordinates":51},"Point",[52,53],-77.10026,38.98067,{"lat":53,"lon":52},[56,61],{"name":57,"role":34,"phone":58,"phoneExt":59,"email":60},"NIH Clinical Center Office of Patient Recruitment (OPR)","800-411-1222","TTY dial 711","ccopr@nih.gov",{"name":62,"role":34,"phone":38,"phoneExt":21,"email":39},"Stephanie Chung, M.D.",{"type":64,"investigatorFullName":21,"investigatorTitle":21,"investigatorAffiliation":21,"oldNameTitle":21,"oldOrganization":21},"SPONSOR","100529081","pilot-study-of-isocaloric-time-restricted-eating-on-ketone-metabolism-and-immunoregulation-100529081",false,"NCT06169137","Pilot Study of Isocaloric Time Restricted Eating on Ketone Metabolism and Immunoregulation","* INCLUSION CRITERIA:\n\nIn order to be eligible to participate in this study, an individual must meet all of the following criteria:\n\n1. Stated willingness to comply with all study procedures and availability for the duration of the study\n2. Women between ages 18-50 years who are premenopausal (defined as regular menses and\u002For FSH \\\u003CULN)\n3. BMI of 18-24.9 or \\>=30 kg\u002Fm\\^2\n4. In good general health as evidenced by medical history and\u002For screening laboratory evaluation.\n5. Agreement to adhere to Lifestyle Considerations throughout study duration\n\nEXCLUSION CRITERIA:\n\nAn individual who meets any of the following criteria will be excluded from participation in this study:\n\n1. Diagnosis\u002Ftreatment for immune\u002Finflammatory disorder or other metabolic conditions that would interfere with study parameters, including diabetes, chronic kidney, chronic liver disease, history of hypoglycemia, and thyroid disease (with the exception of chronic controlled hypothyroidism as measured by TSH within normal limits)\n2. Current use of antihyperglycemic medications, systemic steroids, adrenergic-stimulating agents, or medications affecting sleep, circadian rhythms, or metabolism which affect parameters under investigation (examples include oral contraceptives, anti-diabetic agents, nicotinamide riboside, tryptophan, vitamin B3 supplements)\n3. Caffeine consumption in excess of approximately 300 mg (approximately three 8-oz cups of coffee) daily\n4. Factors that affect circadian rhythms including individuals who perform overnight shift work, report irregular sleep and\u002For eating schedules, and who regularly fast for more than 15 hours\u002Fday\n5. History of an eating disorder by self-report or medical history\n6. Food allergies\u002Fintolerances or dietary patterns that would prohibit consumption of metabolic diet\n7. Inability to provide informed consent\n8. Pregnancy or lactation\n9. Unstable weight with more than 5% body weight change in last previous 3 months\n10. Engaged in competitive sports training and\u002F or unwilling to comply with exercise regimen in this protocol.\n11. Consumption of more than 3 servings of alcohol daily\n12. Current smoker or regular tobacco use, vaping, or other forms of nicotine within prior 3 months\n\nThis study will recruit only women. The study design was informed by our Protocol NCT04728165 which investigates an identical 6:18h TRE intervention in males who are healthy and those with psoriasis. Based on our pilot data in men, the current study is needed to test our hypothesis in women. This study in women is a critical next step to replicate the findings in women and to understand sex-specific differences in TRE response and ketone metabolism.","FEMALE","18 Years","50 Years",{"count":75,"type":76},150,"ESTIMATED","INTERVENTIONAL",[79],"NA","Background:\n\nTime restricted eating (TRE) is a form of fasting in which a person eats only during a set window of time, which is usually between 4 and 10 hours each day. Researchers want to know more about how TRE may affect health.\n\nObjective:\n\nTo learn how TRE affects women with different body sizes.\n\nEligibility:\n\nHealthy women aged 18 to 50 years.\n\nDesign:\n\nParticipants will have 2 visits: 1 screening visit and one 5-day stay in the clinic.\n\nParticipants will fast before both visits. They will have a physical exam with blood tests. They will talk to a nutritionist about the foods they eat. They will lay under a clear hood for up to 45 minutes during a test that measures how many calories they burn while resting.\n\nParticipants will keep a food diary for up to 7 days before their clinic stay. They will apply a continuous glucose monitor the day before they go to the clinic. This is a device that attaches to the skin of the stomach. They will wear this device throughout their clinic stay.\n\nAll meals will be provided during the clinic stay. Participants will follow TRE on 3 days. They will answer survey questions and have tests during their stay, including:\n\n* DXA (dual energy X-ray absorptiometry) scan. Participants will lie on a padded table. Their body will be scanned to measure how much muscle, bone, fat, and other tissues they have.\n* Stable isotope tracer study. Small amounts of sugar and other substances will be given through a tube attached to a needle inserted into a vein in the arm. Blood samples will be collected.",[82,83],"Obesity","Body Weight",[85,86,87,88],"Diet","Time Restricted Eating","Inflammation","Ketone Bodies","2026-05-09",{"date":91,"type":92},"2026-05-12","ACTUAL",{"date":94,"type":92},"2024-09-04",{"date":96,"type":76},"2027-02-05",{"name":29,"class":6},1]