[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100582996":3},{"organization":4,"armGroups":7,"interventions":22,"overallOfficials":27,"centralContacts":31,"locations":37,"responsibleParty":54,"collaborators":57,"id":61,"slug":12,"hasResults":62,"nctId":63,"briefTitle":64,"officialTitle":65,"acronym":66,"eligibilityCriteria":67,"healthyVolunteers":68,"sex":69,"minAge":70,"maxAge":12,"enrollmentInfo":71,"targetDuration":12,"studyType":74,"phases":75,"briefSummary":77,"conditions":78,"keywords":12,"overallStatus":39,"whyStopped":12,"lastUpdateSubmitDate":82,"lastUpdatePostDateStruct":83,"startDateStruct":86,"completionDateStruct":88,"leadSponsor":90,"locationsCount":91},{"fullName":5,"class":6},"University of Washington","OTHER",[8,13,19],{"label":9,"type":10,"description":11,"interventionNames":12},"Focus Group and Child Taste Test (Study 1)","NO_INTERVENTION","No intervention is administered. Adult caregivers will participate in a focus group to assess feasibility of a controlled feeding study in children and children will complete a taste-test of a controlled feeding study menu.",null,{"label":14,"type":15,"description":16,"interventionNames":17},"Study-provided food (Study 2)","EXPERIMENTAL","Participants will be provided all meals for a 7-day period. For the other 7-days of their enrollment, they will be asked to consume their usual diet.",[18],"Other: Diet modification",{"label":20,"type":10,"description":21,"interventionNames":12},"Focus Group (Study 3)","No intervention is administered. Adult caregivers of children will participate in a focus group to learn from families about participating in research involving feeding studies in children.",[23],{"type":6,"name":24,"description":25,"armGroupLabels":26,"otherNames":12},"Diet modification","In Study 2 only, children will be provided all meals for a 7-day period. Meals will consist of nutritious foods, calories provided will exceed the child's estimated daily caloric need, and children will be asked to consume meals ad libitum.",[14],[28],{"name":29,"affiliation":5,"role":30},"Ellen Schur, MD","PRINCIPAL_INVESTIGATOR",[32],{"name":33,"role":34,"phone":35,"phoneExt":12,"email":36},"BRIDGE Study","CONTACT","206 616-6360","bridge-study@uw.edu",[38],{"facility":5,"status":39,"city":40,"state":41,"zip":42,"country":43,"countryCode":44,"cosmosGeoPoint":45,"geoPoint":50,"contacts":51},"RECRUITING","Seattle","Washington","98109","United States","US",{"type":46,"coordinates":47},"Point",[48,49],-122.33207,47.60621,{"lat":49,"lon":48},[52],{"name":33,"role":34,"phone":53,"phoneExt":12,"email":36},"206-616-6360",{"type":30,"investigatorFullName":55,"investigatorTitle":56,"investigatorAffiliation":5,"oldNameTitle":12,"oldOrganization":12},"Ellen Schur, MD, MS","Professor: School of Medicine",[58],{"name":59,"class":60},"National Heart, Lung, and Blood Institute (NHLBI)","NIH","100582996",false,"NCT06870578","Building Research for Intervention Development in Gliosis and Eating Habits","Fostering Patient-oriented Research in Cardiometabolic Disease Pathogenesis and Prevention","BRIDGE","Inclusion Criteria:\n\n* Study1: Adult caregiver and Child age 9-11y. Willing to come to in-person focus group\n* Study 2: Age 9-11y, BMI ≥85th and ≤95th percentile for age and sex\n* Study 3:Adult caregiver with child who qualify for free or reduced-cost lunch in WA State. Child age 9-11y and with overweight.\n\nExclusion Criteria (study 1 child participants and study 3 criteria for children of adult participants):\n\n* Significant health conditions including type 2 diabetes\n* History of major weight loss or eating disorder\n* Current use of medications known to alter appetite or body weight (e.g., stimulants for ADHD)\n* Documented cognitive disorder\n* Severe food allergies, vegetarian, or vegan (Study 1 only)\n* Unable to make the session date\n\nExclusion Criteria (study 2, child participants):\n\n* Significant health conditions including type 2 diabetes\n* History of major weight loss or eating disorder\n* Current use of medications known to alter appetite or body weight (e.g., stimulants for ADHD)\n* Documented cognitive disorder\n* MRI contraindication (e.g., braces, claustrophobia)\n* Weight \\>330 pounds (MRI limit)\n* Severe food allergies, vegetarian, or vegan\n* Currently in formal weight loss program",true,"ALL","9 Years",{"count":72,"type":73},75,"ESTIMATED","INTERVENTIONAL",[76],"NA","The goal of this study is to 1) use magnetic resonance imaging (MRI) to evaluate the effect of nutritious foods on inflammation in the human hypothalamus of children and 2) assess the feasibility and acceptability of nutritious food feeding intervention strategies in children with overweight or obesity.",[79,80,81],"Gliosis","Child Obesity","Eating","2025-06-05",{"date":84,"type":85},"2025-06-06","ACTUAL",{"date":87,"type":85},"2025-04-03",{"date":89,"type":73},"2029-06",{"name":5,"class":6},1]