[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"child-obesity\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:child-obesity":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,12,0,[8,43,71,100,138,163,187,210,235,261,294,314],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":28,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100615765","homegrown-a-family-based-lifestyle-intervention-to-support-healthy-development-of-young-children-with-down-syndrome-100615765",false,"NCT07296861","HomeGrown: A Family-based Lifestyle Intervention to Support Healthy Development of Young Children With Down Syndrome","HomeGrown","Inclusion Criteria:\n\nAdult:\n\n* Ability to provide informed consent\n* 18 years or older\n* Primary caregiver of a child with Down syndrome aged 2 to 6 years old\n* Have access to WI-FI or smartphone\n* Be able to read and speak English\n\nChildren:\n\n* Be 2-6 years old.\n* Are diagnosed with Down syndrome\n* Are not reliant on tube feeding\n\nExclusion Criteria:\n\n\\-",true,"ALL",{"count":19,"type":20},38,"ESTIMATED","INTERVENTIONAL",[23],"NA","The goal of this project is to evaluate an adapted health promotion program, HomeGrown, designed to improve the health of young children with Down syndrome by supporting families in making healthy home environmental changes. There is a significant need for evidence-based programs that address healthy eating and physical activity within this population, as most existing interventions have been developed for typically developing children. By tailoring the program to the unique needs of families of young children with Down syndrome, this project aims to advance inclusion and equity in health behavior promotion.\n\nThis R61\u002FR33 study will assess the feasibility (R61 Phase) and subsequent efficacy (R33 Phase) of the HomeGrown program in improving family practices related to nutrition and physical activity. During the R61 feasibility phase, 38 primary caregivers of children aged 2-6 years with Down syndrome will be enrolled in a 6-month randomized controlled trial. Families will be randomized 1:1 to either the HomeGrown intervention or a waitlist control group (6-month delayed start), stratified by the child's biological sex (male\u002Ffemale) and age (2-3 vs. 4-6 years). All measures will be collected at baseline and at 6-month follow-up.\n\nThe R61 feasibility phase will address three specific aims:\n\nAccrual: Achieve an enrollment rate of 10 families per month, supporting feasibility for the R33 efficacy phase.\n\nEngagement: Demonstrate that families use at least 70% of available HomeGrown intervention components, measured using the digital behavior change interventions engagement scale.\n\nData Collection \\& Retention: Achieve at least 80% retention with completion of all outcome assessments.\n\nBy addressing key gaps in nutrition and physical activity research for young children with Down syndrome, this study has the potential to improve health outcomes for an underserved population and inform future clinical and community health promotion efforts.",[26,27],"Down Syndrome","Child Obesity",[29],"home environmental","RECRUITING","2026-06-09",{"date":33,"type":34},"2026-06-10","ACTUAL",{"date":36,"type":34},"2026-04-16",{"date":38,"type":20},"2027-05",{"name":40,"class":41},"UNC Lineberger Comprehensive Cancer Center","OTHER",1,{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":47,"acronym":4,"eligibilityCriteria":48,"healthyVolunteers":16,"sex":17,"minAge":49,"maxAge":4,"enrollmentInfo":50,"targetDuration":4,"studyType":21,"phases":52,"briefSummary":53,"conditions":54,"keywords":57,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":63,"lastUpdatePostDateStruct":64,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":42},"100604075","family-comida-consumo-de-opciones-ms-ideales-de-alimentos-eating-more-ideal-food-options-100604075","NCT07144800","Family COMIDA (Consumo de Opciones Más Ideales De Alimentos) (Eating More Ideal Food Options)","Inclusion Criteria:\n\nPhase 1\n\n* Age \\>= 18 years (per self-report)\n* Self-identifies as Hispanic\u002FLatino (per self-report)\n* Seeking, or has used, services at the VDS or MHU (per self-report)\n* Is the parent or primary caregiver for at least one child aged 8-12 living in their household (per self-report)\n* Screens as obese (BMI \\> 30 kg\u002Fm2) or overweight (BMI of 25 - 29.9 kg\u002Fm2) (per height and weight measurement in person or per self-report)\n* Owns a cell phone capable of receiving text messages (per self-report)\n* Owns an internet connected device (e.g. cell phone, tablet, etc.) capable of conducting videoconference calls (per self-report)\n* Agrees to be audio-recorded (per self-report)\n\nPhase 2 (parent participants)\n\n* Age \\>= 18 years (per self-report)\n* Self-identifies as Hispanic\u002FLatino (per self-report)\n* Seeking, or has used, services at the VDS or MHU (per self-report)\n* Is the parent or primary caregiver for at least one child aged 8-12 living in their household (per self-report)\n* Screens as obese (BMI \\> 30 kg\u002Fm2) or overweight (BMI of 25 - 29.9 kg\u002Fm2) (per height and weight measurement in person or remotely)\n* Owns a cell phone capable of receiving text messages (per self-report)\n* Owns an internet connected device (e.g. cell phone, tablet, etc.) capable of conducting videoconference calls (per self-report)\n* Agrees to be audio-recorded (per self-report)\n\nPhase 2 (child participants)\n\n* Age 8-12 years (per parent self-report)\n* Has a parent or primary caregiver who is eligible and participating in Phase 2 (per parent self-report)\n\nExclusion Criteria:\n\nPhase 1\n\n* Is pregnant or might be pregnant (per self-report)\n* Presence of a chronic disease such as cancer, kidney disease, liver disease, etc. (individuals with hypertension and diabetes mellitus may still participate) that may affect diet and study participation (per self-report)\n* Has dietary restrictions, i.e. liquid diet, that may affect diet and study participation (per self-report)\n* Has a household member who has already participated or agreed to participate in this study program (per self-report)\n* Prior participation in one of our preliminary studies, e.g., COMIDA, SANOS, Family COMIDA (per self-report) and any related focus groups\n* Works for or with the VDS or MHU (per self-report)\n* Presence of cognitive impairment disorder (i.e., delirium or dementia) sufficient to preclude meaningful informed consent and\u002For data collection (per study team)\n\nPhase 2 (parent participant)\n\n* Is pregnant or might be pregnant (per self-report)\n* For women, is lactating (per self-report)\n* Presence of a chronic disease such as cancer, kidney disease, liver disease, etc. (individuals with hypertension and diabetes mellitus may still participate) that may affect diet and study participation (per self-report)\n* Has dietary restrictions, i.e., liquid diet, that may affect diet and study participation (per self-report)\n* Has physical activity restrictions, i.e., handicapped or mobility issues, that may affect physical activity participation (increasing step counts; per self-report)\n* Has a household member who has already participated or agreed to participate in this study program (per self-report)\n* Prior participation in one of our preliminary studies, e.g., COMIDA, SANOS, Family COMIDA (per self-report) and any related focus groups\n* Works for or with the VDS or MHU (per self-report)\n* Presence of cognitive impairment disorder (i.e., delirium or dementia) sufficient to preclude meaningful informed consent and\u002For data collection (per study team)\n\nPhase 2 (child participant)\n\n* Has dietary restrictions, i.e., liquid diet, that may affect diet and study participation (per parent self-report)\n* Has physical activity restrictions, i.e., handicapped or mobility issues, that may affect physical activity participation (per parent self-report)\n* Has an eating disorder (per parent self-report)\n* Is underweight (per parent self-report)","18 Years",{"count":51,"type":20},1319,[23],"The purpose of this study is to determine the most effective family-centered intervention (FCI) for weight loss and obesity prevention in Hispanic families. FCI is a type of program that involves family (such as parents and caregivers) supporting their children to promote healthy habits.",[55,27,56],"Obesity","Weight Loss",[58,59,60,61,62],"child obesity","obesity","weight loss","Memorial Sloan Kettering Cancer Center","25-003","2026-04-14",{"date":65,"type":34},"2026-04-15",{"date":67,"type":34},"2025-08-22",{"date":69,"type":20},"2031-07-31",{"name":61,"class":41},{"id":72,"slug":73,"hasResults":11,"nctId":74,"briefTitle":75,"officialTitle":75,"acronym":76,"eligibilityCriteria":77,"healthyVolunteers":11,"sex":17,"minAge":78,"maxAge":49,"enrollmentInfo":79,"targetDuration":4,"studyType":81,"phases":4,"briefSummary":82,"conditions":83,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":90,"lastUpdatePostDateStruct":91,"startDateStruct":93,"completionDateStruct":95,"leadSponsor":97,"locationsCount":99},"100616404","a-multicenter-retrospective-analysis-of-postoperative-respiratory-complications-in-children-with-obstructive-sleepapnea-100616404","NCT07305168","A Multicenter Retrospective Analysis of Postoperative Respiratory Complications in Children With Obstructive Sleepapnea","MRA PORC","Inclusion Criteria:\n\n* scheduled for (adeno)tonsillectomy as treatment for OSAS\n\nExclusion Criteria:\n\n* other surgery than (adeno)tonsillectomy performed as treatment for OSAS\n* Polysomnography not available within 1 year before surgery","1 Year",{"count":80,"type":20},200,"OBSERVATIONAL","This retrospective observational study aims to evaluate postoperative respiratory complications (PORC) after (adeno)tonsillectomy in children with OSA.\n\nIn order to increase the number of patients available for analysis, we will merge data collected at UZA with data collected at the the Department of Sleep Laboratory and Sleep Surgery at the Heim Pal National Pediatric Institute, Hungary. These colleagues performed an identical prospective data collection.",[84,85,86,27,87,88,89],"Obstructive Sleep Apnea","Postoperative Respiratory Complications","Adenotonsillectomy","Craniofacial Abnormalities","Children With Down Syndrome","Neurologic Disorder","2025-12-11",{"date":92,"type":34},"2025-12-26",{"date":94,"type":34},"2022-05-02",{"date":96,"type":20},"2027-03-01",{"name":98,"class":41},"University Hospital, Antwerp",2,{"id":101,"slug":102,"hasResults":11,"nctId":103,"briefTitle":104,"officialTitle":105,"acronym":106,"eligibilityCriteria":107,"healthyVolunteers":16,"sex":17,"minAge":108,"maxAge":109,"enrollmentInfo":110,"targetDuration":4,"studyType":21,"phases":112,"briefSummary":113,"conditions":114,"keywords":118,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":128,"lastUpdatePostDateStruct":129,"startDateStruct":131,"completionDateStruct":133,"leadSponsor":135,"locationsCount":137},"100542308","effect-of-sleep-extension-on-body-weight-and-learning-in-children-more2sleep-100542308","NCT06341179","Effect of Sleep Extension on Body Weight and Learning in Children (More2Sleep)","A Randomized Controlled Trial of Sleep Extension to Regulate Body Weight and Improve Learning in School-aged Children","More2Sleep","Inclusion Criteria:\n\n* Age: 6-12 years old (inclusive range).\n* Weight status: having a BMI above average, defined as an age- and sex-specific BMI Z-score above zero using reference standards from the WHO.\n* Sleep duration: sleeping ≤9 h\u002Fnight on the basis of sleep diaries filled in by the children's parents, based on recommendations by the American Academy of Sleep Medicine and the Sleep Health Foundation.\n\nExclusion Criteria:\n\n* Any genetic, neurological, endocrinological or psychiatric condition that affects growth, metabolism, eating behaviors, cognitive function, or body weight (for example: dwarfism, epilepsy, attention deficit hyperactivity disorder, head trauma, β-thalassemia, hypothyroid-ism, hyperthyroidism, type I diabetes).\n* Any sleep-related disorder (for example: obstructive sleep apnea, parasomnias, narcolepsy, restless leg syndrome).\n* Regular use of prescribed or over-the-counter medications that influence study outcomes.\n* Irregular school schedule.\n* If a child's parents live separately, the child is allowed to sleep at both households. How-ever, if one of the parents does not wish to carry out the sleep intervention and follow given instructions, then the child should only sleep at their household Friday, Saturday and\u002For Sunday night.\n* In the circumstance where the child does not speak or understand Danish, the child's parents do not have to speak or understand Danish, as long as both parties can speak and understand English.\n* Participation in other research studies.\n* Metal implants and claustrophobia (only for substudy-II).","6 Years","12 Years",{"count":111,"type":20},142,[23],"More2Sleep is a randomized, controlled, parallel trial with two groups (sleep extension vs control) including 142 school-aged children (6-12 years) who have a BMI above average, defined as age- and sex-specific BMI Z-score above zero using WHO reference standards, and habitually sleep for ≤ 9 h\u002Fnight. Data will be collected before and after a 3-month sleep extension intervention, and after a 6-month follow-up (at months 0, 3, and 9). The collection of data is mainly related to the main study. However, some optional examinations will be conducted on a first come, first serve basis, consisting of substudy-I (metabolic mechanisms, n=60) and substudy-II (learning mechanisms, n=142).\n\nThe primary objective is to assess the effects of sleep extension by \\~45 min\u002Fnight, achieved by going to bed 60-90 min earlier, on adiposity and learning ability in school-aged children who have a BMI for age and sex above average, and sleep less than recommended for their age.",[115,27,116,117],"Sleep Duration","Child Development","Child Behavior",[119,120,121,122,123,124,125,126,127],"Sleep duration","Sleep quality","Overweight and Obesity","Energy Intake","Child Development and Behavior","Well-being","Cognitive Function","Learning Ability","Memory","2025-11-19",{"date":130,"type":34},"2025-11-25",{"date":132,"type":34},"2024-08-13",{"date":134,"type":20},"2028-12-31",{"name":136,"class":41},"University of Copenhagen",3,{"id":139,"slug":140,"hasResults":11,"nctId":141,"briefTitle":142,"officialTitle":143,"acronym":4,"eligibilityCriteria":144,"healthyVolunteers":11,"sex":17,"minAge":108,"maxAge":145,"enrollmentInfo":146,"targetDuration":4,"studyType":21,"phases":148,"briefSummary":149,"conditions":150,"keywords":152,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":154,"lastUpdatePostDateStruct":155,"startDateStruct":157,"completionDateStruct":159,"leadSponsor":161,"locationsCount":42},"100559943","evaluating-the-impact-of-a-school-based-fruit-and-vegetable-co-op-on-cardiometabolic-child-and-parents-health-in-a-persistent-poverty-area-100559943","NCT06570707","Evaluating the Impact of a School-based Fruit and Vegetable Co-op on Cardiometabolic Child and Parents Health in a Persistent Poverty Area","Cluster-Randomized Controlled Trial (RCT) to Evaluate the Impact of a School-based Fruit and Vegetable Co-op on Cardiometabolic Health of Children and Parents in a Persistent Poverty Area","Inclusion Criteria:\n\n* enrollment of 100 1st, 2nd, and 3rd grade students\n* high proportion of children participating in the free and reduced lunch (FRL) program (\\>70%)\n* willingness to implement a coordinated school health (CSH) program\n\nExclusion Criteria:\n\n* Prior participation in BB in the previous school year\n* children or parents identified as special needs per school; or having any physical, cognitive, or psychological disability that would prevent participation in evaluation measures","9 Years",{"count":147,"type":20},720,[23],"The purpose of this study is to examine the effects of the (Brighter Bites (BB) intervention compared to a wait-list control group 9 months after the intervention on changes in primary child outcomes (HbA1c, and vegetable intake), on changes in secondary outcomes (household food security status, parent and child dietary behaviors, and home access\u002Favailability of fruits and vegetables (FV)), and the mediational influence of changes in food security status, parent outcomes, and home environment measures on changes in child outcomes.",[27,151],"Cardiometabolic Health",[153],"Brighter Bites","2025-07-02",{"date":156,"type":34},"2025-07-08",{"date":158,"type":34},"2024-08-08",{"date":160,"type":20},"2027-06-30",{"name":162,"class":41},"The University of Texas Health Science Center, Houston",{"id":164,"slug":165,"hasResults":11,"nctId":166,"briefTitle":167,"officialTitle":168,"acronym":169,"eligibilityCriteria":170,"healthyVolunteers":16,"sex":17,"minAge":145,"maxAge":4,"enrollmentInfo":171,"targetDuration":4,"studyType":21,"phases":173,"briefSummary":174,"conditions":175,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":178,"lastUpdatePostDateStruct":179,"startDateStruct":181,"completionDateStruct":183,"leadSponsor":185,"locationsCount":42},"100582996","building-research-for-intervention-development-in-gliosis-and-eating-habits-100582996","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",{"count":172,"type":20},75,[23],"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.",[176,27,177],"Gliosis","Eating","2025-06-05",{"date":180,"type":34},"2025-06-06",{"date":182,"type":34},"2025-04-03",{"date":184,"type":20},"2029-06",{"name":186,"class":41},"University of Washington",{"id":188,"slug":189,"hasResults":11,"nctId":190,"briefTitle":191,"officialTitle":192,"acronym":4,"eligibilityCriteria":193,"healthyVolunteers":16,"sex":17,"minAge":49,"maxAge":4,"enrollmentInfo":194,"targetDuration":4,"studyType":21,"phases":196,"briefSummary":197,"conditions":198,"keywords":4,"overallStatus":200,"whyStopped":4,"lastUpdateSubmitDate":201,"lastUpdatePostDateStruct":202,"startDateStruct":204,"completionDateStruct":206,"leadSponsor":208,"locationsCount":4},"100591272","healthy-start-family-childcare-providers-and-parents-100591272","NCT06978270","Healthy Start: Family Childcare Providers and Parents","Healthy Start: An Innovative, Multi-level Intervention With Family Childcare Providers and Families to Improve the Dietary Behaviors of Pre-school Children","Providers:\n\nInclusion Criteria:\n\n* English and\u002For Spanish-speaking and reading\n* State licensed family childcare providers (FCCP)\n* FCCP that care for 18-54 month-old children,\n* Plan for FCCH to be in operation for the next year\n* Willing to be randomized to either study arm,\n* Have at least 2 eligible children in their care with at least 1 parent-child dyad consenting to participate\n\nExclusion Criteria:\n\n* Participation in the prior Healthy Start Project\n\nParents:\n\nInclusion Criteria:\n\n* English and\u002For Spanish-speaking and reading\n* Legal guardian of child(ren) who receive care in a participating FCCH\n* Child(ren) must be 18-54 months-old\n* Care must be for at least 15 hrs.\u002Fwk\n* Plan to continue childcare with their current FCCP for the next 9 months\n* Be the caregiver mainly responsible for the child's eating at home\n* Willing to be randomized (with the FCCP) to either study arm\n\nExclusion Criteria:\n\n* Not meeting above criteria.\n\nChildren:\n\nInclusion Criteria:\n\n* Children 18-54 months-old who receive care in a participating FCCH\n* Care must be for at least 15 hours per week\n* Agree to be measured (All other evaluation is observation that does not require assent).\n\nExclusion Criteria:\n\n\\- Not meeting above criteria.",{"count":195,"type":20},40,[23],"The preschool years are a critical time for shaping food preferences and eating behaviors, which affect dietary behaviors in adults and life-long risks for obesity, diabetes, cardiovascular disease, and other chronic conditions. Unfortunately, many US children, especially low-income and ethnic minorities, have dietary patterns associated with obesity and increased morbidity. Thus, to improve child diet quality, it is essential to develop effective targeted interventions in settings where children (especially higher-risk children) spend time. The investigators build upon our efficacious Healthy Start intervention with family childcare home (FCCH) providers (FCCP) to pilot a novel, 8-month multilevel tailored intervention to reach families through FCCH. This would be the first study to incorporate family-based intervention components into FCCH. The 8-month intervention will include an adapted version of the Healthy Start intervention as well as FCCP training to deliver nutrition messages to parents using an existing childcare App, complemented with FCCH environmental cues and tailored print and videos for parents. In sum, feasible and effective interventions to improve young children's diets are urgently needed. The FCCH is a novel and untapped setting to intervene with both FCCP and parents simultaneously to affect children's diets in both childcare and home settings, which has the potential to more fully impact the child's overall diet and weight status.",[27,199],"Nutrition, Healthy","NOT_YET_RECRUITING","2025-05-29",{"date":203,"type":34},"2025-06-03",{"date":205,"type":20},"2025-06-15",{"date":207,"type":20},"2026-03-31",{"name":209,"class":41},"Brown University",{"id":211,"slug":212,"hasResults":11,"nctId":213,"briefTitle":214,"officialTitle":215,"acronym":4,"eligibilityCriteria":216,"healthyVolunteers":16,"sex":17,"minAge":217,"maxAge":108,"enrollmentInfo":218,"targetDuration":4,"studyType":21,"phases":220,"briefSummary":221,"conditions":222,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":226,"lastUpdatePostDateStruct":227,"startDateStruct":229,"completionDateStruct":231,"leadSponsor":233,"locationsCount":42},"100524392","food-for-thought-executive-functioning-around-eating-among-children-100524392","NCT06108128","Food for Thought: Executive Functioning Around Eating Among Children","Characterizing Top-down Dimensions of Appetite Self-regulation Among Preschoolers","Inclusion Criteria:\n\n1. Child ages 4 to 6 years of age\n2. Caregiver reporting primary responsibility for child feeding outside of childcare\n3. Caregiver legal guardian\n\nExclusion Criteria:\n\n1. Caregiver \\\u003C18 years of age\n2. Child major food allergies\n3. Child medication use, developmental disability, or medical conditions known to affect food intake and\u002For growth; color blindness\n4. Child in foster care","4 Years",{"count":219,"type":20},125,[23],"Scientific knowledge of the cognitive-developmental processes that serve to support children's appetite self-regulation are surprisingly limited. This investigation will provide new scientific directions for obesity prevention by elucidating cognitive-developmental influences on young children's ability to make healthy food choices and eat in moderation.",[223,224,225,27],"Self-regulation","Appetitive Behavior","Eating Behavior","2025-04-07",{"date":228,"type":34},"2025-04-10",{"date":230,"type":34},"2023-10-05",{"date":232,"type":20},"2025-12-31",{"name":234,"class":41},"Temple University",{"id":236,"slug":237,"hasResults":11,"nctId":238,"briefTitle":239,"officialTitle":240,"acronym":241,"eligibilityCriteria":242,"healthyVolunteers":16,"sex":17,"minAge":243,"maxAge":244,"enrollmentInfo":245,"targetDuration":4,"studyType":21,"phases":247,"briefSummary":248,"conditions":249,"keywords":250,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":252,"lastUpdatePostDateStruct":253,"startDateStruct":255,"completionDateStruct":257,"leadSponsor":259,"locationsCount":42},"100539415","more-outside-your-door-a-dietphysical-activity-intervention-to-decrease-risk-of-obesity-in-alaska-native-preschoolers-100539415","NCT06303544","More Outside Your Door: a Diet\u002Fphysical Activity Intervention to Decrease Risk of Obesity in Alaska Native Preschoolers","More Outside Your Door (MOYD): a Multilevel Intervention Promoting Traditional Diet and Physical Activity to Decrease Risk of Obesity in Alaska Native (AN) Preschoolers","MOYD","Inclusion Criteria:\n\n* parent who identifies as Alaska Native (AN)\n* parental consent\n* enrolled in preschool in one of the12 participating Head Start programs\n* present at school for health screenings\n\nExclusion Criteria:\n\n* lack of parental consent\n* does not have a parent who is AN","3 Years","5 Years",{"count":246,"type":20},450,[23],"The preschool age is a crucial period of growth and an optimal time to begin to establish healthy eating and physical activity habits leading to better food and activity choices into adulthood, thereby minimizing risk for obesity-related diseases and decreasing the cardiometabolic disparities in this Indigenous population. More Outside Your Door is a multi-level, randomized, stepped-wedge intervention trial designed to reduce the disparity of childhood obesity in Yup'ik Alaska Native children by increasing the proportion of nutrient-dense traditional and traditional-like foods offered and increasing physical activity, particularly outdoor activities related to traditional Yup'ik subsistence and lifestyle practices. This 5-year intervention trial targeting 3-5 year olds is conducted in partnership with Rural Action Community Action Program Head Start programs in 12 rural Alaskan communities, where each site is assigned annually to a wedge group to receive either a community-altered culturally-tailored 8-month traditional foods and activities curriculum intervention or the standard regional Head Start program intervention.",[27],[251],"Head Start, CBPR","2025-01-27",{"date":254,"type":34},"2025-01-29",{"date":256,"type":34},"2024-09-01",{"date":258,"type":20},"2028-05-30",{"name":260,"class":41},"Alaska Native Tribal Health Consortium",{"id":262,"slug":263,"hasResults":11,"nctId":264,"briefTitle":265,"officialTitle":265,"acronym":266,"eligibilityCriteria":267,"healthyVolunteers":16,"sex":17,"minAge":244,"maxAge":109,"enrollmentInfo":268,"targetDuration":4,"studyType":21,"phases":270,"briefSummary":271,"conditions":272,"keywords":280,"overallStatus":200,"whyStopped":4,"lastUpdateSubmitDate":285,"lastUpdatePostDateStruct":286,"startDateStruct":288,"completionDateStruct":290,"leadSponsor":292,"locationsCount":42},"100576898","improvements-in-daily-activity-and-exercise-in-school-children-the-actchild-study-100576898","NCT06791278","Improvements in Daily Activity and Exercise in School Children: the ActChild Study","ActChild","Inclusion Criteria:\n\n* Schoolchildren, 0.-1. Grade, 5-8 years of age,\n* Resident in Aarhus Municipality\n\nExclusion Criteria:\n\n\\- None",{"count":269,"type":20},600,[23],"The goal of this clinical trial is to assess the health-related effects of an exercise intervention in children aged 5-8 years.\n\nMain research questions:\n\n* Does a municipality-driven exercise intervention improve physical activity levels in children?\n* Does a municipality-driven exercise intervention improve sleep parameters in children?\n* Does a municipality-driven exercise intervention improve eating behaviors in children?\n* Does a municipality-driven exercise intervention improve quality of life in children?\n\nStudy Design:\n\nParticipants will be assigned to either:\n\n* Intervention group: Attend 1-2 weekly sessions of 45-60 minutes of child-friendly exercise for 1 year.\n* Control group: Receive no intervention.\n\nData Collection:\n\nParticipants will:\n\n* Complete questionnaires at baseline, and at 1-year, 3-year, and 5-year follow-ups.\n* Wear accelerometers for 7 consecutive days at baseline, and at 1-year, 3-year, and 5-year follow-ups.",[273,274,275,276,117,277,278,279,27],"Healthy Children","Children","Children in School","Child Health","Physical Activity","Sleep","Eating Behaviors",[281,274,282,283,225,278,277,284],"Exercise Intervention","School Children","CEBQ","Quality of Life","2025-01-22",{"date":287,"type":34},"2025-01-24",{"date":289,"type":20},"2025-02-04",{"date":291,"type":20},"2032-12",{"name":293,"class":41},"University of Aarhus",{"id":295,"slug":296,"hasResults":11,"nctId":297,"briefTitle":298,"officialTitle":299,"acronym":4,"eligibilityCriteria":300,"healthyVolunteers":11,"sex":17,"minAge":109,"maxAge":301,"enrollmentInfo":302,"targetDuration":4,"studyType":21,"phases":303,"briefSummary":304,"conditions":305,"keywords":4,"overallStatus":200,"whyStopped":4,"lastUpdateSubmitDate":306,"lastUpdatePostDateStruct":307,"startDateStruct":309,"completionDateStruct":311,"leadSponsor":313,"locationsCount":42},"100547385","brighter-biteslegacy-produce-rx-program-100547385","NCT06407284","Brighter Bites\u002FLegacy Produce Rx Program","Brighter Bites & Legacy Community Health Produce Rx: Evaluating the Feasibility and Effectiveness of a School-based Clinical Nutrition Program With Produce Prescription","Inclusion Criteria:\n\n* Must be a patient at one of the four Legacy Community Health School-based clinics in Galena Park, Texas\n* BMI greater than or equal to 85th percentile\n* reside within a 10-mile radius of Houston Food Bank\n* Medicaid recipients or low-income uninsured\n* parents must be able to read and write in English or Spanish to complete surveys\n* patient and parents must confirm their willingness to complete the participant's well-child visit for the entire period of the study (approximately one year).\n\nExclusion Criteria:\n\n* currently participating in Brighter Bites\n* with a family member\u002Fsibling currently participating in Brighter Bites","17 Years",{"count":269,"type":20},[23],"The purpose of this study is to assess the effectiveness of the produce prescription program at improving weight status and obesity-related health outcomes of participants, to examine the impacts of the program on household food insecurity and nutrition security, to examine the impacts of the program on participating adolescents' dietary behavioral outcomes, their home nutrition environment and feeding practices and to examine the impacts of the program in reducing healthcare use and associated costs",[27],"2025-01-08",{"date":308,"type":34},"2025-01-10",{"date":310,"type":20},"2025-01-15",{"date":312,"type":20},"2026-08-31",{"name":162,"class":41},{"id":315,"slug":316,"hasResults":11,"nctId":317,"briefTitle":318,"officialTitle":319,"acronym":4,"eligibilityCriteria":320,"healthyVolunteers":16,"sex":17,"minAge":244,"maxAge":109,"enrollmentInfo":321,"targetDuration":4,"studyType":21,"phases":323,"briefSummary":324,"conditions":325,"keywords":4,"overallStatus":200,"whyStopped":4,"lastUpdateSubmitDate":327,"lastUpdatePostDateStruct":328,"startDateStruct":330,"completionDateStruct":332,"leadSponsor":334,"locationsCount":42},"100558094","a-structured-school-based-health-intervention-for-the-obesity-prevention-100558094","NCT06546644","A Structured School-based Health Intervention for the Obesity Prevention","Effect of a Structured School-based Health Intervention for Obesity Prevention In Children Aged 5-12 Years","Inclusion Criteria:\n\n* Children of age between 5 to 12 years.\n* Enrollment at one of the selected schools.\n\nExclusion Criteria:\n\n* Children and their parents who did not give assent and consent to participate in the study.",{"count":322,"type":20},1200,[23],"The proposed research aims to assess how well a structured intervention is intended to reduce childhood obesity. The intervention addresses food and physical activity behaviors, important determinants of obesity, by concentrating on these elements. The goal of nutritional and physical education is to raise knowledge about the negative effects of obesity and encourage healthy eating habits in children and their caregivers. These educational campaigns will be delivered primarily through schools, guaranteeing a wide audience and consistent messaging.",[27,117,326],"Obesity, Childhood","2024-08-07",{"date":329,"type":34},"2024-08-09",{"date":331,"type":20},"2024-08-15",{"date":333,"type":20},"2025-04-15",{"name":335,"class":41},"Universiti Putra Malaysia"]