[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"eating-behaviors\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:eating-behaviors":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,13,0,[8,48,74,97,116,141,161,184,225,262,286,319,340],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":24,"conditions":25,"keywords":29,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100239105","children-s-growth-and-behavior-study-100239105",false,"NCT02390765","Children s Growth and Behavior Study","Children's Growth and Behavior Study","* Eligibility Criteria for Parents\u002FGuardians of Child Participants:\n\nINCLUSION CRITERIA:\n\nParents\u002FGuardians will qualify if they meet the following criteria.\n\n1. Age \\>=18 years\n2. Have a child enrolled in this protocol (15-CH-0096).\n\nEXCLUSION CRITERIA:\n\nParents\u002FGuardians will be excluded for the following reasons:\n\n1. If their child is not eligible to participate in the study (see below)\n2. If they are believed by the medical study team to have a medical or psychiatric problem that will not allow them to complete study procedures safely (these will be determined on a case-by-case basis)\n\n   Eligibility Criteria for Child Participants:\n\n   INCLUSION CRITERIA:\n\n   Volunteers will qualify if they meet the following criteria.\n   * Age 8-17 years (NB: children may continue to participate as adults during follow-up).\n   * Weight, height and BMI \\>= 5th percentile for age and sex according to Centers for Disease Control and Prevention 2000 US standards.\n   * Cognitively capable of completing study procedures (FSIQ \\>= 70).\n   * Good general health based on a normal history and physical examination (with the exception of overweight and minor, well-controlled illnesses).\n\n   EXCLUSION CRITERIA:\n\n   Individuals will be excluded (and provided treatment referrals as needed) for the following reasons:\n   * History of major cardiovascular disease or any other serious obesity-related complication as assessed during history and physical exam. Individuals with untreated or major illnesses relating to the endocrine and\u002For cardiovascular systems are excluded because these illnesses will likely influence outcomes. Such obesity-related comorbidities include hypertension (defined by age- sex- and height- specific standards; and fasting hyperglycemia consistent with diabetes (fasting glucose \\> 126 mg\u002FdL).\n   * Presence of other major illnesses: renal, hepatic, gastrointestinal, most endocrinologic (e.g., Cushing syndrome, untreated hyper- or hypothyroidism), hematological problems or pulmonary disorders (other than asthma not requiring continuous medication). Non-serious medical illnesses, such as seasonal allergies, will be reviewed on a case-by-case basis.\n   * Regular use of any medication known to affect body weight or eating behavior (e.g., many medications prescribed for attention deficit hyperactivity disorder, or ADHD). Medication use for non-serious conditions (e.g., acne) will be considered on a case-by-case basis.\n   * Current pregnancy or a history of pregnancy. A negative pregnancy test before starting the study will be required for postmenarcheal girls.\n   * Current and regular use of tobacco products and\u002For alcohol.\n   * A significant reduction in weight during the past three months, for any reason, exceeding 5% of body weight.\n   * A history of significant or recent brain injury that may considerably influence performance on neurocognitive measures (i.e., any history of loss of consciousness \\>=30 minutes associated with a head injury, any history of memory loss or hospitalization associated with a head injury, or \\>=2 concussions within last year).\n   * Presence of any significant, full-threshold psychiatric disorder based on DSM criteria such as schizophrenia, bipolar disorder, alcohol or substance abuse, anorexia or bulimia nervosa, or any disorder that, in the opinion of the investigators, would impede competence or compliance or possibly hinder completion of the study. These individuals will not be permitted to enroll in the current study and will be referred for treatment. Individuals who present with other psychiatric disorders, including sub-threshold psychiatric disorders, will be permitted to enroll in the study. Sub-threshold psychiatric disorders include symptoms that do not meet diagnostic threshold based on the DSM criteria for mental disorders, but which are nevertheless significantly impairing or distressing. If, based on the opinion of the investigators, a participant requires treatment for his\u002Fher psychiatric symptoms, the individual will be referred for treatment. Participants who develop any psychiatric disorder or significant psychiatric symptoms at any follow-up assessment during the study will not be excluded, but will be provided with treatment referrals.\n   * Any other condition in the child or parents\u002Fguardians that, in the opinion of the investigators, would impede compliance or possibly hinder completion of the study (e.g., significant Learning Disorder).\n\n   Additional exclusions for (optional) stool sample collection include:\n\n   Stool Sample only:\n   * Diagnosis or history of inflammatory bowel disease, including ulcerative colitis or Crohn's disease, celiac sprue, irritable bowel syndrome, or other inflammatory disorders of the intestine.\n   * Diarrhea within 1 week prior to sampling.\n   * Antibiotic use within 4 weeks prior to sampling.\n\n   In addition, Experiments 1 and 2 have specific additional exclusions:\n\n   Experiment 1 only:\n   * Regular use of medications that could influence autonomic or endocrine functioning, including alpha and beta blockers, oral contraceptives, or prescription pain medication.\n   * Scoring as \"highly active\" on the International Physical Activity Questionnaire (due to decreased cortisol reactivity).\n\n   Experiment 2 only:\n   * Participants will be excluded if MRI and MEG is contraindicated (metal in\u002Fon body, braces, presence of non-organic \\[e.g., cochlear\\] implants or cerebral clips, permanent tattooed makeup or general tattoos that are recent and\u002For in a dangerous location on the body or made with colors whose content in iron cannot be definitely ruled out.\n   * Youth will be excluded if they are left-handed.\n\n   All participants will receive a written explanation of the purposes, procedures, and potential hazards of the study. Communication of this information and of the participant's assent as well as the consent of the parent or guardian will be documented in the medical record and copies of all signed documents given to each family. All participants will be informed of their right to withdraw from the study.",true,"ALL","8 Years","100 Years",{"count":21,"type":22},1500,"ESTIMATED","OBSERVATIONAL","Background:\n\n\\- Studies show that many factors affect children's eating behavior and health. These include sleep, mood, thinking skills, and genetics. Studying children over time may identify children at higher risk for eating-related health concerns.\n\nObjective:\n\n\\- To understand how genes and environment influence eating behavior and health over time.\n\nEligibility:\n\n\\- Children ages 8-17 in good general health.\n\nDesign:\n\n* Screening visit 1: Medical history, physical exam, body measurements, and questions.\n* 14 days: Participants will wear a wrist monitor and answer smartphone prompts about eating and mood. They may give a stool sample.\n* Screening visit 2:\n* Body measurements.\n* Saliva, urine, and blood samples.\n* Heart tests.\n* Meals provided (after fasting overnight).\n* Questionnaires and interview.\n* Behavior, thinking, and exercise tests.\n* X-ray of left wrist and full body.\\\u003CTAB\\>\n* Some parents may have medical history, physical exam, and questions at screening visits. They may answer questions at the yearly visits.\n* Participants will have up to 6 yearly visits. They will give a urine sample and body measurements, and repeat the X-rays. They will have questions and behavior and thinking tasks. They may give stool samples. Visits will range from 3 to 8 hours.\n* Participants may choose to participate in other studies:\n* Stress and Hormones, 1 visit: While resting, participants will give saliva samples and have their heart monitored. Then they will do math. They will repeat the resting part, then do a computer task.\n* Brain Imaging, 2 visits: Twice, participants will perform tasks with a magnetic cone on their head then answer questions. Once, they will have an MRI, lying still in a scanner with a coil on their head. Before the first visit, participants will collect at-home saliva samples once a day for three days. During both visits, participants will perform tasks and answer questions that gauge their thinking skills and mood.\n* Experiment 3 (sleep\u002Ffatigue): Participants will complete 2 additional visits. During these visits, participants will complete a task on the computer for 2 hours, or watch a movie for two hours. After completion of the task\u002Fmovie, they will answer questions and be provided with food.\n\nParticipants will be compensated for the time and inconvenience involved with completing study procedures.\n\n...",[26,27,28],"Obesity","Eating Behaviors","Healthy Volunteers",[30,31,32,26,33,34],"Stress Response","Binge Eating","Eating Behavior","Disordered Eating","Natural History","RECRUITING","2026-07-01",{"date":38,"type":39},"2026-07-02","ACTUAL",{"date":41,"type":39},"2015-04-21",{"date":43,"type":22},"2030-12-31",{"name":45,"class":46},"Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)","NIH",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":54,"eligibilityCriteria":55,"healthyVolunteers":11,"sex":17,"minAge":56,"maxAge":57,"enrollmentInfo":58,"targetDuration":4,"studyType":60,"phases":61,"briefSummary":63,"conditions":64,"keywords":4,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":68,"completionDateStruct":69,"leadSponsor":71,"locationsCount":4},"100645411","the-influence-of-water-intake-on-snack-intake-in-children-100645411","NCT07680647","The Influence of Water Intake on Snack Intake in Children","Investigating the Influence of Consuming Water as a Beverage on Intake of a Snack in Children","Kids Water","Inclusion Criteria:\n\n* Like, are willing to eat study food\n* Does not have allergies, food restrictions or health issues that prevent them from consuming study food\n* Will attend summer camp during both of the scheduled study visits\n\nExclusion Criteria:\n\n\\-","6 Years","12 Years",{"count":59,"type":22},50,"INTERVENTIONAL",[62],"NA","The primary purpose of this study is to investigate the influence of including water as a beverage at a snack on food intake in children.",[27],"NOT_YET_RECRUITING","2026-06-29",{"date":38,"type":39},{"date":66,"type":22},{"date":70,"type":22},"2026-09-15",{"name":72,"class":73},"Cornell University","OTHER",{"id":75,"slug":76,"hasResults":11,"nctId":77,"briefTitle":78,"officialTitle":79,"acronym":4,"eligibilityCriteria":80,"healthyVolunteers":11,"sex":17,"minAge":81,"maxAge":4,"enrollmentInfo":82,"targetDuration":4,"studyType":60,"phases":84,"briefSummary":85,"conditions":86,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":88,"lastUpdatePostDateStruct":89,"startDateStruct":91,"completionDateStruct":93,"leadSponsor":95,"locationsCount":47},"100603360","early-time-restricted-eating-in-older-adults-with-hypertension-100603360","NCT07135505","Early Time-Restricted Eating in Older Adults With Hypertension","The Effect of Early Time-Restricted Eating on Cardiometabolic Health and Circadian Rhythms in Hypertensive Older Adults With Habitual Prolonged Eating Window","Inclusion Criteria:\n\n* Consent to participate in the study\n* Men and women ≥ 60 years old\n* Average office systolic BP ≥130 mmHg\n* Self-reported ≥12 hours eating period per day of at least 5 days\u002Fweek\n* Stable health history over the past 2 months\n\nExclusion Criteria:\n\n* Fasting \\>12 hours per day\n* Actively trying to lose weight by participating in formal weight loss program or significantly restricting calorie intake\n* Have lost ≥ 10 pounds in last 3 months\n* Unable to wake up at a regular time between 6-8 am\n* Perform overnight shift work more than 1day\u002Fweek on average\n* Resting heart rate of \\>120 beats per minute, systolic blood pressure \\> 180 mmHg and\u002For diastolic blood pressure of \\> 100 mmHg\n* Have been diagnosed with diabetes\n* On insulin or diabetes medication\n* Unstable angina, heart attack or stroke in the past 3 months\n* Continuous use of supplemental oxygen to manage a chronic pulmonary condition or heart failure\n* Pregnant or breastfeeding\n* Rheumatoid arthritis, Parkinson's disease or currently on dialysis\n* Current diagnosis of a major psychiatric condition that would impair study participation\n* Severe gastrointestinal disease, major gastrointestinal surgery, or active gallstone disease\n* Active treatment for cancer in the past year\n* Taking medications that preclude fasting for 16 hours (e.g. must be taken with food at least 12 hours apart)","60 Years",{"count":83,"type":22},30,[62],"The purpose of this study is to find out how early time-restricted eating affects body rhythms and improves cardiometabolic health in older adults.",[87,27],"Hypertension","2026-06-18",{"date":90,"type":39},"2026-06-22",{"date":92,"type":39},"2026-02-16",{"date":94,"type":22},"2028-07-31",{"name":96,"class":73},"University of Alabama at Birmingham",{"id":98,"slug":99,"hasResults":11,"nctId":100,"briefTitle":101,"officialTitle":101,"acronym":102,"eligibilityCriteria":103,"healthyVolunteers":11,"sex":17,"minAge":104,"maxAge":81,"enrollmentInfo":105,"targetDuration":4,"studyType":60,"phases":106,"briefSummary":107,"conditions":108,"keywords":4,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":109,"lastUpdatePostDateStruct":110,"startDateStruct":112,"completionDateStruct":113,"leadSponsor":115,"locationsCount":47},"100644415","the-combined-effects-of-energy-density-and-variety-on-intake-100644415","NCT07663214","The Combined Effects of Energy Density and Variety on Intake","VarxED","Inclusion Criteria:\n\n* Regularly consume 3 meals per day\n* Like, are willing to eat, and do not have allergies to the study foods\n* Are willing to refrain from drinking alcohol the day before study visits\n* Are willing to consume a consistent breakfast the day of study visits\n* Have a BMI between 18.5-29.9 kg\u002Fm2\n\nExclusion Criteria:\n\n* Experienced a weight change \\>5 kg in the past month\n* Are a smoker\n* Are an athlete in training\n* Take medications or have a health condition known to affect appetite\n* Are pregnant or breastfeeding\n* Have ever been diagnosed with an eating disorder or depression\n* Specialize in the fields of psychology or nutritional sciences.","20 Years",{"count":59,"type":22},[62],"The primary purpose of this study is to investigate the influence independent fn combined influence of variety and energy density on food intake at a meal. Additionally, individual characteristics will be examined for their influence on the effects of variety and energy density on intake.",[27],"2026-06-17",{"date":111,"type":39},"2026-06-23",{"date":36,"type":22},{"date":114,"type":22},"2027-07-31",{"name":72,"class":73},{"id":117,"slug":118,"hasResults":11,"nctId":119,"briefTitle":120,"officialTitle":121,"acronym":4,"eligibilityCriteria":122,"healthyVolunteers":16,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":123,"targetDuration":4,"studyType":60,"phases":125,"briefSummary":126,"conditions":127,"keywords":128,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":132,"lastUpdatePostDateStruct":133,"startDateStruct":135,"completionDateStruct":137,"leadSponsor":139,"locationsCount":47},"100587457","supper-heroes-examining-the-impact-of-an-online-eating-intervention-for-families-100587457","NCT06928636","Supper Heroes: Examining the Impact of an Online Eating Intervention for Families","Supper Heroes: Randomized Controlled Trial to Examine the Impact of an Online Environmentally Friendly Eating Intervention for Families","Inclusion Criteria:\n\n* have at least one child 9-12 years old\n* live in Ontario, Canada\n* have access to the internet\n* can respond to English surveys\n\nExclusion Criteria:\n\n* parent(s) with prior nutrition and food education (e.g., degree in nutrition, culinary arts training)\n* families with food allergies that would prevent them from participating in the intervention (e.g., soy products, beans or lentils)\n* families who are vegetarian or vegan",{"count":124,"type":22},330,[62],"This study will examine the effectiveness of the online family-based program focused on sustainable eating compared to weekly emails about environmentally friendly behaviours.",[27],[129,130,131],"food waste","environmentally friendly","plant-based foods","2026-06-04",{"date":134,"type":39},"2026-06-08",{"date":136,"type":39},"2025-07-09",{"date":138,"type":22},"2027-12",{"name":140,"class":73},"University of Guelph",{"id":142,"slug":143,"hasResults":11,"nctId":144,"briefTitle":145,"officialTitle":145,"acronym":146,"eligibilityCriteria":147,"healthyVolunteers":11,"sex":17,"minAge":104,"maxAge":81,"enrollmentInfo":148,"targetDuration":4,"studyType":60,"phases":150,"briefSummary":151,"conditions":152,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":153,"lastUpdatePostDateStruct":154,"startDateStruct":156,"completionDateStruct":158,"leadSponsor":160,"locationsCount":47},"100626712","the-influence-of-water-intake-on-food-intake-at-meals-varying-in-moisture-100626712","NCT07439198","The Influence of Water Intake on Food Intake at Meals Varying in Moisture","WaterxMoisture","Inclusion Criteria:\n\n* 20 - 60 years old\n* Regularly consume 3 meals per day\n* Like, are willing to eat, and do not have restrictions or allergies to the study foods\n* Are willing to refrain from drinking alcohol the day before study visits\n* Are willing to consume a consistent breakfast the day of study visits\n* Have a BMI between 20-29.9 kg\u002Fm2\n\nExclusion Criteria:\n\n* Experienced a weight change \\>5 kg in the past month\n* Are a smoker\n* Are an athlete in training\n* Take medications or have a health condition known to affect taste, smell, thirst, or appetite\n* Are pregnant or breastfeeding\n* Have ever been diagnosed with an eating disorder or depression\n* Specialize in the fields of psychology or nutritional sciences",{"count":149,"type":22},60,[62],"The primary purpose of this study is to investigate the influence of including water as a beverage at a meal on food intake, and if the influence of water consumption on food consumption is moderated by switching behavior. Additionally, other individual characteristics will be examined for their influence on the effects of simultaneous variety and portion size on meal intake.",[27],"2026-04-21",{"date":155,"type":39},"2026-04-23",{"date":157,"type":39},"2026-03-15",{"date":159,"type":22},"2027-02-23",{"name":72,"class":73},{"id":162,"slug":163,"hasResults":11,"nctId":164,"briefTitle":165,"officialTitle":166,"acronym":4,"eligibilityCriteria":167,"healthyVolunteers":16,"sex":17,"minAge":168,"maxAge":169,"enrollmentInfo":170,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":172,"conditions":173,"keywords":4,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":175,"lastUpdatePostDateStruct":176,"startDateStruct":178,"completionDateStruct":180,"leadSponsor":182,"locationsCount":4},"100614893","eating-behaviors-in-children-and-adolescents-withwithout-celiac-disease-100614893","NCT07285512","Eating Behaviors in Children and Adolescents With\u002FWithout Celiac Disease","Eating Behaviors in Children and Adolescents With\u002FWithout Celiac Disease: A Cross-Sectional and Longitudinal Study","Inclusion Criteria:\n\nCeliac Disease Group (Cases)\n\n* Adolescents aged 11 to 17 years\n* Confirmed diagnosis of celiac disease according to the European Society for Paediatric Gastroenterology, Hepatology and Nutrition (ESPGHAN) criteria (positive serology and\u002For duodenal biopsy)\n* Ability to understand and complete questionnaires in Italian\n* For the longitudinal cohort: diagnosis \\\u003C 6 months prior to enrollment\n\nHealthy Control Group\n\n* Adolescents aged 11 to 17 years\n* No diagnosis of celiac disease\n* Ability to understand and complete questionnaires in Italian\n\nExclusion Criteria:\n\n* Significant cognitive impairment or developmental disorders preventing questionnaire completion\n* Inadequate understanding of the Italian language\n* Refusal or inability to provide assent\u002Fconsent","11 Years","17 Years",{"count":171,"type":22},300,"This observational study investigates the prevalence and severity of disordered eating behaviors in adolescents aged 11-17 years with celiac disease. Participants complete validated self-report questionnaires (Youth Eating Disorder Examination Questionnaire, YEDE-Q, and Parent Eating Disorder Examination Questionnaire, PEDE-Q) and a structured clinical form. A healthy control group, matched by age and sex, is included for comparison. A longitudinal sub-cohort diagnosed with celiac disease \\\u003C6 months prior will be followed at 6, 12, and 24 months to evaluate changes in eating psychopathology and associated clinical variables.",[174,27],"Celiac Disease in Children","2025-12-12",{"date":177,"type":39},"2025-12-16",{"date":179,"type":22},"2025-12-15",{"date":181,"type":22},"2028-12-15",{"name":183,"class":73},"IRCCS San Raffaele",{"id":185,"slug":186,"hasResults":11,"nctId":187,"briefTitle":188,"officialTitle":189,"acronym":190,"eligibilityCriteria":191,"healthyVolunteers":11,"sex":17,"minAge":192,"maxAge":169,"enrollmentInfo":193,"targetDuration":4,"studyType":60,"phases":195,"briefSummary":196,"conditions":197,"keywords":205,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":216,"lastUpdatePostDateStruct":217,"startDateStruct":219,"completionDateStruct":221,"leadSponsor":223,"locationsCount":47},"100582507","addressing-weight-bias-internalization-to-improve-adolescent-weight-management-outcomes-randomized-pilot-trial-100582507","NCT06864208","Addressing Weight Bias Internalization to Improve Adolescent Weight Management Outcomes: Randomized Pilot Trial","Piloting an Intervention to Address Weight Bias Internalization to Improve Adolescent Weight Management Outcomes","SWIFT","Inclusion Criteria:\n\n* Speak English;\n* 13-17 years of age;\n* BMI at or above \\>95th%ile for age and sex;\n* Have at least one caregiver available to provide consent and participate in sessions;\n* Agree to study participation;\n\nExclusion Criteria:\n\n* Cognitive impairment or developmental delay impairing participation in a group setting;\n* Current participation in a weight management program or recent weight loss of 5% of body weight or more;\n* Medical condition known to impact weight or that would otherwise prevent participation;\n* Current use of glucagon-like peptide-1 (GLP-1) receptor agonists;","13 Years",{"count":194,"type":22},64,[62],"Weight stigma and weight bias internalization (WBI) are common among adolescents at higher weight statuses. WBI is associated with negative physical and mental health outcomes. The current study aims to test an intervention for weight stigma and WBI combined with an evidence-based adolescent weight management program. Eligible adolescents (13-17) will be assigned by chance to one of two groups: 1) a 4-week intervention focused on weight stigma and WBI followed by a 16-week behavioral weight management program; or 2) a 4-week health information control (to include non-weight-related health promotion topics such as smoking and skin cancer prevention) followed by the same 16-week weight management program but without the WBI and weight stigma content. Study outcomes will be assessed at the 4-week and post-treatment (20 week) timepoints.",[198,199,200,201,202,203,204,27],"Weight","Body Weight","Weight Bias","Weight Stigma","Physiological Stress","Biological Markers of Stress","Biological Markers of Inflammation",[206,207,198,208,209,210,211,212,213,214,215],"Adolescents","Teens","C-reactive protein","CRP","Interleukin-6","IL-6","Eating behaviors","Behavioral weight management","Weight bias","Weight stigma","2025-09-22",{"date":218,"type":39},"2025-09-24",{"date":220,"type":39},"2025-03-25",{"date":222,"type":22},"2027-02",{"name":224,"class":73},"The Miriam Hospital",{"id":226,"slug":227,"hasResults":11,"nctId":228,"briefTitle":229,"officialTitle":230,"acronym":4,"eligibilityCriteria":231,"healthyVolunteers":16,"sex":232,"minAge":233,"maxAge":234,"enrollmentInfo":235,"targetDuration":4,"studyType":60,"phases":237,"briefSummary":238,"conditions":239,"keywords":243,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":253,"lastUpdatePostDateStruct":254,"startDateStruct":256,"completionDateStruct":258,"leadSponsor":260,"locationsCount":47},"100601564","non-diet-nutrition-education-and-its-effects-on-eating-behavior-body-image-and-well-being-in-adult-women-100601564","NCT07112131","Non-Diet Nutrition Education and Its Effects on Eating Behavior, Body Image, and Well-Being in Adult Women","The Effect of Non-Diet Nutrition Education on Eating Behavior, Body Image, and Well-Being in Adult Women: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Female,\n* Aged between 19-35 years,\n* Body Mass Index (BMI) between 18.5-24.9,\n\nExclusion Criteria:\n\n* Pregnant or breastfeeding,\n* Diagnosed eating disorder or other psychiatric condition,\n* Currently enrolled in a weight loss program,\n* Following a restrictive diet due to medical conditions.","FEMALE","19 Years","35 Years",{"count":236,"type":22},52,[62],"The goal of this clinical trial is to evaluate whether a non-diet nutrition education program can improve eating behaviors, body image, and well-being in normal-BMI women aged 19-35 years. The main questions it aims to answer are:\n\n* Does participation in an 8-week non-diet nutrition education program improve eating behavior, body image, and well-being over time in the intervention group compared to the control group?\n* Is there a significant difference between the intervention and control groups in eating behavior, body image, and well-being after the intervention?\n\nResearchers will compare an intervention group receiving an 8-week non-diet nutrition education with a control group receiving no intervention, to see if the program leads to improvements in psychological and behavioral outcomes without focusing on weight loss.\n\nParticipants will:\n\n* Complete pre- and post-intervention assessments, including validated questionnaires on eating behavior (DEBQ, FCQ, IES-2), body image (BAS, Stunkard Figure Rating Scale), and psychological well-being (WHO-5, Rosenberg Self-Esteem Scale), as well as a 3-day food diary.\n* Be randomly assigned to either the intervention group (8-week online non-diet nutrition education sessions) or the control group (no intervention).\n* Engage in 8 weekly, 60-minute sessions focused on intuitive eating, body acceptance, and health-promoting nutrition.",[27,240,241,242],"Body Image","Well-Being, Psychological","Young Adult Females",[244,245,246,247,248,249,250,251,252],"Non-diet approach","Intuitive eating","Body acceptance","Body image","Eating behavior","Psychological well-being","Young adult women","Nutrition education","Randomized controlled trial","2025-08-01",{"date":255,"type":39},"2025-08-08",{"date":257,"type":39},"2025-07-21",{"date":259,"type":22},"2025-10",{"name":261,"class":73},"Tuğba TÜRKCAN",{"id":263,"slug":264,"hasResults":11,"nctId":265,"briefTitle":266,"officialTitle":267,"acronym":268,"eligibilityCriteria":269,"healthyVolunteers":16,"sex":232,"minAge":270,"maxAge":234,"enrollmentInfo":271,"targetDuration":4,"studyType":60,"phases":272,"briefSummary":273,"conditions":274,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":277,"lastUpdatePostDateStruct":278,"startDateStruct":280,"completionDateStruct":282,"leadSponsor":284,"locationsCount":47},"100589919","nature-for-body-image-100589919","NCT06960668","Nature for Body Image","Look at the Bright (Nature) Side: Improving Body Image and Associated Protective Factors and Reducing Body Image Threats With the Nature for Body Image (NBI) Project","NBI","Inclusion Criteria:\n\n* Females\n* Age 18-35 years old\n\nExclusion Criteria:\n\n* Full-blown body image disorder","18 Years",{"count":149,"type":22},[62],"Nature exposure has been found to be particularly beneficial for body image, as recent studies have identified a positive association between time spent in nature and positive body image. Positive body image, defined as the ability to accept and respect one's body, has been linked to greater life satisfaction and engagement in healthy behaviors. Conversely, negative body image is recognized as a public health concern due to its detrimental effects on both physical and mental health. It has been associated with symptoms of Body Image Disorders (BIDs), including Eating Disorders (EDs) and Body Dysmorphic Disorder (BDD).\n\nThe Nature for Body Image (NBI) project aimed to examine the impact of a structured nature exposure intervention on improving body image among young women aged 18-35 years.",[240,27,275,276],"Self-Compassion","Interoception","2025-05-15",{"date":279,"type":39},"2025-05-16",{"date":281,"type":39},"2025-05-01",{"date":283,"type":22},"2026-02-28",{"name":285,"class":73},"University of Padova",{"id":287,"slug":288,"hasResults":11,"nctId":289,"briefTitle":290,"officialTitle":290,"acronym":291,"eligibilityCriteria":292,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":270,"enrollmentInfo":293,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":295,"conditions":296,"keywords":302,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":310,"lastUpdatePostDateStruct":311,"startDateStruct":313,"completionDateStruct":315,"leadSponsor":317,"locationsCount":47},"100587463","pediatric-feeding-disorder-evolution-in-amiens-university-hospital-100587463","NCT06928714","Pediatric Feeding Disorder Evolution in Amiens University Hospital","EVOLTOA","Inclusion Criteria:\n\n* Children \\\u003C18 years old\n* with at least two pediatric gastroenterology PFDs consultations at CHUAP ,\n* with an inapropriate oral intakes for at least 2 weeks,\n* Association with medical, nutritional, psychosocial or eating-skills dysfunction.\n\nExclusion Criteria:\n\n* anorexia nervosa",{"count":294,"type":22},33,"Pediatric feeding disorders (PFDss) affect children with age-inappropriate oral intakes lasting at least 2 weeks, associated with medical, nutritional, psychosocial or feeding skills dysfunction. Feeding is a complex function involving the digestive tract, and different structures. It evolves throughout the child's development. It involves the caregiver-child relationship. Dysfunction of one or more of these systems may be the cause of pediatric feeding disorders. PFDs affect 25% of children, 5% with severe forms. PFDs can have severe nutritional consequences. They often cause malnutrition, even undernutrition, and sometimes overweight.",[297,27,298,299,300,301],"Feeding Disorders","Dysphagia","Nutritional Status","Malnutrition","Children",[303,304,305,306,307,308,309],"feeding disorders","eating behavior","dysphagia","nutritional status","malnutrition","artificial nutrition","children","2025-04-08",{"date":312,"type":39},"2025-04-15",{"date":314,"type":39},"2025-03-01",{"date":316,"type":22},"2025-05",{"name":318,"class":73},"Centre Hospitalier Universitaire, Amiens",{"id":320,"slug":321,"hasResults":11,"nctId":322,"briefTitle":323,"officialTitle":324,"acronym":325,"eligibilityCriteria":326,"healthyVolunteers":16,"sex":232,"minAge":270,"maxAge":234,"enrollmentInfo":327,"targetDuration":4,"studyType":60,"phases":329,"briefSummary":330,"conditions":331,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":333,"lastUpdatePostDateStruct":334,"startDateStruct":335,"completionDateStruct":337,"leadSponsor":339,"locationsCount":47},"100571787","yoga-4-body-image-y4bi-investigating-the-impact-of-yoga-on-body-image-and-eating-behaviours-100571787","NCT06724796","Yoga 4 Body Image (Y4BI): Investigating the Impact of Yoga on Body Image and Eating Behaviours","Yoga 4 Body Image (Y4BI): Investigating the Impact of Yoga on Body Image and Eating Behaviours in Young Women","Y4BI","Inclusion Criteria:\n\n* Females\n* Age 18-35 years old\n\nExclusion Criteria:\n\n* Regular yoga practice\n* Pregnancy\n* Medical conditions that preclude yoga practice (e.g., neurodegenerative diseases, recent injuries, rheumatic conditions)\n* Full-blown body image disorder",{"count":328,"type":22},100,[62],"The practice of yoga can positively impact body image, a psychological construct encompassing perceptual, emotional, cognitive, and behavioral aspects, which can be either positive or negative. Negative body image manifests as extreme dissatisfaction with one's body-a condition particularly common among young women-that places them at significant risk for developing Body Image Disorders (BIDs). In contrast, positive body image is characterized by an overall respect for one's body.\n\nCurrent research on the impact of yoga on body image has several limitations, making it challenging to determine whether yoga practice truly has a positive effect on body image and to identify the mechanisms underlying this impact. To address these gaps, the present project aims to overcome the limitations of existing studies by investigating the impact of yoga on body image through quantitative methodologies and by exploring the mechanisms that drive this effect.\n\nThe project consists of two phases:\n\n1. Investigating the impact of yoga on body image (both positive and negative) and eating behaviours in a population characterized by high levels of body dissatisfaction-young women.\n2. Examining the psychological mechanisms underlying yoga's impact on body image, including increased interoceptive awareness, embodiment, and self-compassion, as well as a reduction in self-objectification.",[332,240,27],"Body Dissatisfaction","2025-03-24",{"date":220,"type":39},{"date":336,"type":39},"2024-11-30",{"date":338,"type":22},"2026-07-31",{"name":285,"class":73},{"id":341,"slug":342,"hasResults":11,"nctId":343,"briefTitle":344,"officialTitle":344,"acronym":345,"eligibilityCriteria":346,"healthyVolunteers":16,"sex":17,"minAge":347,"maxAge":57,"enrollmentInfo":348,"targetDuration":4,"studyType":60,"phases":350,"briefSummary":351,"conditions":352,"keywords":360,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":365,"lastUpdatePostDateStruct":366,"startDateStruct":368,"completionDateStruct":370,"leadSponsor":372,"locationsCount":47},"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","5 Years",{"count":349,"type":22},600,[62],"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.",[353,301,354,355,356,357,358,27,359],"Healthy Children","Children in School","Child Health","Child Behavior","Physical Activity","Sleep","Child Obesity",[361,301,362,363,32,358,357,364],"Exercise Intervention","School Children","CEBQ","Quality of Life","2025-01-22",{"date":367,"type":39},"2025-01-24",{"date":369,"type":22},"2025-02-04",{"date":371,"type":22},"2032-12",{"name":373,"class":73},"University of Aarhus"]