[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"obesity-adolescent\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:obesity-adolescent":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,11,0,[8,43,67,93,122,160,198,229,260,286,316],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100366076","pain-and-weight-treatment-development-and-trial-of-paw-100366076",false,"NCT04046562","Pain and Weight Treatment: Development and Trial of PAW","PAW","Inclusion Criteria:\n\n* Males and females between 12 and 18 years of age\n* Ability to speak, write and read English\n* A parent or guardian who speaks, writes and reads English\n* Signed consent and assent from the child and parent\n* Enrollment in a weight management program\n* Score greater than 3 on the Pain Burden Inventory at screening (in order to recruit adolescents who experience more than just general aches and pains).\n* Youth reporting musculoskeletal pain\n\nExclusion Criteria:\n\n* Parent or guardian unable to participate\n* Patients on weight reducing medications\n* Severe psychiatric illness (i.e., suicidal or hospitalization within past 6 months)\n* Medical conditions such as Type 1 diabetes","ALL","12 Years","18 Years",{"count":20,"type":21},50,"ESTIMATED","INTERVENTIONAL",[24],"NA","Pediatric weight management efficacy is impacted by failure to complete treatment protocols and, for those that do complete treatment, a return to unhealthy behaviors. This project tests whether treating pain, a common comorbid condition to pediatric obesity, will enhance treatment. This study will generate results that can be translated into immediate improvements in care for families seeking treatment for pediatric obesity.",[27,28,29],"Obesity, Adolescent","Pain, Chronic","CBT","RECRUITING","2026-06-29",{"date":33,"type":34},"2026-07-01","ACTUAL",{"date":36,"type":34},"2019-08-14",{"date":38,"type":21},"2027-06",{"name":40,"class":41},"Connecticut Children's Medical Center","OTHER",1,{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":4,"eligibilityCriteria":49,"healthyVolunteers":11,"sex":16,"minAge":50,"maxAge":18,"enrollmentInfo":51,"targetDuration":4,"studyType":22,"phases":53,"briefSummary":55,"conditions":56,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":58,"lastUpdatePostDateStruct":59,"startDateStruct":61,"completionDateStruct":63,"leadSponsor":65,"locationsCount":42},"100404831","phase-2-oxytocin-for-weight-loss-in-adolescents-100404831","NCT04551482","Oxytocin for Weight Loss in Adolescents","Oxytocin as a Neuroendocrine Therapy for Obesity in Youth","Inclusion Criteria:\n\n* Males and Females, 10-18 years\n* Obesity (BMI ≥95th percentile for age and gender)\n* Willingness to maintain current diet and lifestyle for the duration of study participation\n\nExclusion Criteria:\n\n* Current substance abuse\n* Use of prescription or over-the-counter drugs or dietary\u002Fherbal supplements that may affect weight if dose increased in the three months preceding the baseline visit and\u002For if they plan to increase the dose during the 18 weeks of study participation.\n* Greater than 5kg weight loss over 3 months;\n* Follows a nonstandard diet (e.g., Paleo, Atkins, raw diet, macrobiotic diet)\n* Cardiovascular disease\n* Prolonged QT interval\n* Chronic inflammatory bowel disease and other inflammatory conditions\n* Epilepsy\n* TSH \\> 2.5 times upper limit of normal\n* Alanine transaminase (ALT) or aspartate transaminase (AST) \\>2.5 times upper limit of normal\n* Creatinine \\>1.5 mg\u002Fdl\n* Hyponatremia\n* Pregnancy\u002Fbreastfeeding or refusal to use contraception not containing estrogen throughout the study if female and sexually active\n* MRI exclusion criteria such as the presence of a pacemaker or cerebral aneurysm clips\n* Weight \\>450 lbs due to limits for MRI and DXA scanners\n* Type 1 Diabetes Mellitus or Type 2 Diabetes Mellitus if HbA1c \\>8%\n* Active eating disorder","10 Years",{"count":52,"type":21},55,[54],"PHASE2","This is a randomized, double blind, placebo-controlled study of the effects of intranasal oxytocin in youths with obesity, ages 10-18 years old. Subjects will be randomized to receive intranasal oxytocin or placebo (1 spray per nostril, 4 times per day) for 12 weeks. Study visits include screening to determine eligibility, 2-part main study visits at baseline, week 8, and week 12, and safety check-in visits at weeks 1, and 4; phone calls at weeks 2, 6, and 10, with a safety follow-up visit 6 weeks after the last dose of study drug. Study procedures include appetite, behavioral, metabolic, and endocrine assessments.",[27,57],"Oxytocin","2026-06-23",{"date":60,"type":34},"2026-06-26",{"date":62,"type":34},"2021-07-28",{"date":64,"type":21},"2027-02-28",{"name":66,"class":41},"Massachusetts General Hospital",{"id":68,"slug":69,"hasResults":11,"nctId":70,"briefTitle":71,"officialTitle":72,"acronym":73,"eligibilityCriteria":74,"healthyVolunteers":75,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":76,"targetDuration":4,"studyType":22,"phases":78,"briefSummary":79,"conditions":80,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":83,"lastUpdatePostDateStruct":84,"startDateStruct":86,"completionDateStruct":88,"leadSponsor":90,"locationsCount":92},"100586859","multi-modal-digital-interventions-for-adolescent-weight-management-100586859","NCT06920862","Multi-Modal Digital Interventions for Adolescent Weight Management","Effectiveness of Multi-Modal Digital Interventions for Adolescent Weight Management: A Randomized Controlled Trial","M2DI-AWM","Inclusion Criteria:\n\n* Adolescents aged 12-18 years.\n* Body Mass Index (BMI) ≥ 85th percentile according to the Health Promotion Administration (HPA) standards.\n* Willing to participate in a digital intervention for weight control.\n* At least one parent or guardian provides consent for participation.\n* Able to understand and use digital devices (smartphones, tablets, or computers).\n\nExclusion Criteria:\n\n* Significant communication barriers (e.g., severe speech, hearing, or cognitive impairments).\n* Psychiatric disorders that affect interpersonal interaction (e.g., schizophrenia, severe depression).\n* Previous negative experiences with digital health interventions (VR or AI-based coaching).\n* Severe motion sickness that affects the ability to use VR-based tools.\n* Currently enrolled in another weight management program that may interfere with study outcomes.",true,{"count":77,"type":21},200,[24],"The goal of this randomized controlled trial is to evaluate the effectiveness of a multi-modal digital intervention, based on the Theory of Planned Behavior (TPB), in promoting healthy weight control behaviors among overweight and obese adolescents. This study also aims to reduce the risk of unhealthy weight control behaviors by leveraging artificial intelligence-driven coaching, interactive platforms, gamified applications, and real-time feedback mechanisms.\n\nThe main questions this study aims to answer are:\n\n1. Can a multi-modal digital intervention effectively modify adolescents' primary beliefs underlying TPB constructs (attitude, subjective norms, and perceived behavioral control)?\n2. How do TPB constructs influence weight control intentions, and how do these intentions translate into either healthy or unhealthy weight control behaviors? What role do adolescents' body image, body satisfaction, and mental health play in moderating the relationship between weight control intention and behavior?\n\nParticipants will:\n\n1. Be adolescents aged 12-18 years with a BMI ≥ 85th percentile.\n2. Be randomly assigned to either the intervention group (multi-modal digital intervention) or the control group (general health education).\n3. Engage in AI-driven coaching, interactive digital sessions, and gamified experiences tailored to TPB constructs.\n4. Complete biweekly sessions over a period of three months (each session lasting two hours).\n5. Receive personalized feedback and real-time monitoring through the Virti platform.\n6. Participate in follow-up assessments at one month and three months post-intervention.\n\nResearchers will compare the intervention group to the control group to determine whether the multi-modal digital intervention leads to a higher adoption of healthy weight control behaviors and a lower prevalence of unhealthy weight control behaviors.",[27,81,82],"Weight Change, Body","Weight Stigma","2026-04-06",{"date":85,"type":34},"2026-04-13",{"date":87,"type":34},"2025-08-01",{"date":89,"type":21},"2029-12-31",{"name":91,"class":41},"National Yang Ming Chiao Tung University",2,{"id":94,"slug":95,"hasResults":11,"nctId":96,"briefTitle":97,"officialTitle":98,"acronym":4,"eligibilityCriteria":99,"healthyVolunteers":75,"sex":16,"minAge":100,"maxAge":18,"enrollmentInfo":101,"targetDuration":4,"studyType":103,"phases":4,"briefSummary":104,"conditions":105,"keywords":108,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":83,"lastUpdatePostDateStruct":114,"startDateStruct":116,"completionDateStruct":118,"leadSponsor":120,"locationsCount":5},"100514772","national-blood-pressure-screening-in-children-to-improve-paediatric-healthcare-in-south-africa-100514772","NCT05982847","National Blood Pressure Screening in Children to Improve Paediatric Healthcare in South Africa","National Blood Pressure Screening in Children to Optimise Clinical Management of Paediatric Hypertension in South Africa","Inclusion Criteria:\n\n* All children between ages 5-\\\u003C18 years\n* All children with voluntary assent\u002Fconsent and parent's permission\n\nExclusion Criteria:\n\n* circumstances interfere with the participant's ability to give informed consent (diminished understanding or comprehension, or any language barriers that may pose potential risk in participation under false expectations)\n* randomly selected children who choose not to participate (lack of assent\u002Fconsent), even if parent's permission was received,\n* conditions that interfere with a patient's ability to follow study guidelines, e.g., the use of drugs, alcohol or tobacco products\n* ages \\>18 years or under 5 years\n* Children will be excluded from the analysis for the determination of normative reference values for blood pressure and anthropometry if taking certain concomitant medication(s) that may affect their blood pressure, or any underlying disease e.g., chronic kidney disease, chronic heart disease etc. that may raise blood pressure.","5 Years",{"count":102,"type":21},22464,"OBSERVATIONAL","The Childhood Hypertension Consortium of South Africa (CHCSA) was established to foster relationships between the healthcare sector and schools through community engagement and outreach as well as contributing to the decolonization of normative paediatric blood pressure reference values. To date, there has been no nation-wide project in South Africa to determine nationally representative normal blood pressure reference values, nor to estimate the true prevalence of hypertension in the paediatric population of the country. This study will provide critical information on the understanding of blood pressure and hypertension in children, especially of African ancestry. Not only will this effort contribute to the development of the first nationally representative normal reference values of blood pressure but will also benefit healthcare providers in the sector with a clear guideline on the management of high blood pressure in children as developed by experts working with these challenges daily.",[106,27,107],"Hypertension","Obesity, Childhood",[109,110,111,112,113],"Adiposity","Blood Pressure","Cardiovascular Diseases","Health Knowledge, Attitudes, Practice","Lifestyle Factors",{"date":115,"type":34},"2026-04-07",{"date":117,"type":34},"2024-04-01",{"date":119,"type":21},"2028-11-30",{"name":121,"class":41},"North-West University, South Africa",{"id":123,"slug":124,"hasResults":11,"nctId":125,"briefTitle":126,"officialTitle":127,"acronym":128,"eligibilityCriteria":129,"healthyVolunteers":75,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":130,"targetDuration":4,"studyType":22,"phases":132,"briefSummary":133,"conditions":134,"keywords":139,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":151,"lastUpdatePostDateStruct":152,"startDateStruct":154,"completionDateStruct":156,"leadSponsor":157,"locationsCount":159},"100610097","a-sensory-strategy-to-cut-sugary-beverages-in-africanamerican-and-latine-adolescents-100610097","NCT07223151","A Sensory Strategy to Cut Sugary Beverages in African\u002FAmerican and Latine Adolescents","Trading Sugar for Sparkles in Adolescents, A Sensory Approach for Reducing Added Sugar From Sweetened Beverages","SPARKLE","Inclusion Criteria:\n\n* Adolescents ages 12 to 18 who display a \"sweet-liker\" pattern, characterized by a preference for higher concentrations of sugar in beverages, specifically identifying 0.3M (10.3% sucrose) or above as their most liked sample.\n* Have obesity (body mass index \\[BMI\\] \\> 95%). During screening, subjects' height and weight will be measured to calculate BMI, and BMI will be balanced across study arms using stratified randomization.\n* Adolescents must also indicate a willingness to drink study beverages; not currently dieting\u002Fchanging diet.\n\nExclusion Criteria:\n\n* For the primary objective. Exclusion Criteria:\n\n  * Adolescent participant is pregnant, since pregnancy affects taste perception\n  * Participant is allergic or intolerant to the items we are testing.\n\nFor the secondary objective. Exclusion Criteria:\n\n* Adolescent with type 1 or type 2 diabetes (self-declared or detected at screening visit through fasting glucose)\n* Currently consume unsweetened, sparkling water two or more times per week.\n* Adolescent participant is pregnant, since pregnancy affects taste perception\n* Participant is allergic or intolerant to the items we are testing.\n* Allergic or intolerant to the items that we are testing.",{"count":131,"type":21},63,[24],"The goal of this clinical trial is to test whether replacing sugary sodas with unsweetened, flavored sparkling waters can reduce added sugar intake and improve health in Black\u002FAfrican American and Latine adolescents with obesity who prefer sweet-tasting beverages. The main questions it aims to answer are:\n\n* Does replacing sugary sodas with water change liking for sugary drinks, and water?\n* Do shifts in liking for sweetness lead to improved diet quality and cardiometabolic health?\n\nResearchers will compare replacing sugary sodas with one of three alternative beverages: unsweetened sparkling water, plain water, and beverages with gradually reduced sugar to determine which strategy is most effective.\n\nParticipants will:\n\n* Replace sugary sodas with study drinks for 4 weeks\n* Complete taste tests to measure their liking for and sensory experience of sweetness over 8-weeks\n* Provide dietary recalls, body measurements, and blood samples over 8-weeks",[27,135,136,137,138],"Dietary Sugars","Taste Perception","Insulin Resistance","Feeding Behavior",[140,141,142,136,137,143,144,145,146,147,148,149,150],"Obesity","Adolescent","Sugar-Sweetened Beverages","Sweet Taste Preference","Latine Youth","African American Youth","Dietary Intervention","Beverage Replacement","Sugar Reduction","Sensory Evaluation","Randomized Controlled Trial","2025-10-29",{"date":153,"type":34},"2025-10-31",{"date":155,"type":34},"2025-07-25",{"date":38,"type":21},{"name":158,"class":41},"Nana Gletsu Miller",3,{"id":161,"slug":4,"hasResults":11,"nctId":162,"briefTitle":163,"officialTitle":164,"acronym":165,"eligibilityCriteria":166,"healthyVolunteers":75,"sex":16,"minAge":167,"maxAge":4,"enrollmentInfo":168,"targetDuration":4,"studyType":22,"phases":170,"briefSummary":171,"conditions":172,"keywords":180,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":189,"lastUpdatePostDateStruct":190,"startDateStruct":192,"completionDateStruct":194,"leadSponsor":196,"locationsCount":42},"100579291","NCT06822387","Health Without Barriers\u002FSalud Sin Barreras- Northern Colorado","Growing an Extension Network for Multisite Dissemination and Implementation of Intensive Health Behavior and Lifestyle Treatment","HWB\u002FSSB","Inclusion Criteria:\n\nAdolescent subjects\n\n* Between the ages 11-19 years old\n* Reside in Larimer County, Weld County, or the surrounding areas.\n\nParent\u002Fguardian subjects:\n\n* 18 years old or older\n* Are parents\u002Fguardians of an adolescent between the ages of 11-19\n* Reside in Larimer County, Weld County, or the surrounding areas\n\nFacilitators subjects\n\n* 18 years old or older\n* Reside in Larimer County, Weld County, or the surrounding areas\n* Are planning to or have facilitated HWB\n\nExclusion Criteria\n\nAdolescents subjects will not take part in the research activities if they have a medical and\u002For psychological\u002Fbehavioral condition that, in the opinion of the Colorado State University\u002FExtension program team, could interfere with safety for themselves or others or interfere with the capability of the participant or other participants to potentially benefit from the program (e.g., severe emotional-behavioral disturbance, inability to follow facilitator directions).\n\nParents\u002Fguardians will not take part in the research activities if they have a medical and\u002For psychological\u002Fbehavioral condition that, in the opinion of the Colorado State University\u002FExtension program team, could interfere with safety for themselves or others or interfere with the capability of their family or other participating families to potentially benefit from the program (e.g., using drugs or alcohol or under the use of drugs\u002Falcohol during program sessions, aggressive or inappropriate behavior toward other participants).\n\nThere is no exclusion for facilitator subjects.","11 Years",{"count":169,"type":21},140,[24],"The overarching goal of this work is to address the limited access to evidence-based health behavior and lifestyle interventions for youth and families most impacted by preventable chronic diseases, including obesity and type 2 diabetes. In the current project, we implement a small single-arm pilot and feasibility trial of Health Without Barriers\u002FSalud Sin Barreras (HWB\u002FSSB), a culturally-adapted, whole-family intensive health behavior and lifestyle intervention to 11-19-year-old adolescents and their families living in Northern Colorado. Objectives are refining the HWB\u002FSSB community facilitator training, evaluating the feasibility and acceptability of HWB\u002FSSB implementation, and characterizing changes in health outcomes among adolescent participants.",[173,174,175,176,177,178,179,27],"Lifestyle Risk Reduction","Adolescent Health","Family Health","Cardio-metabolic Health","Mental Health","Wellness Program","Type 2 Diabetes",[181,182,183,184,185,186,187,188],"Whole-family","Mindfulness","Wellness education","Nutrition","Physical Activity","Stress reduction","Health Without Barriers","Salud Sin Barreras","2025-04-29",{"date":191,"type":34},"2025-05-02",{"date":193,"type":34},"2025-04-07",{"date":195,"type":21},"2026-06-30",{"name":197,"class":41},"Colorado State University",{"id":199,"slug":200,"hasResults":11,"nctId":201,"briefTitle":202,"officialTitle":203,"acronym":4,"eligibilityCriteria":204,"healthyVolunteers":11,"sex":16,"minAge":18,"maxAge":4,"enrollmentInfo":205,"targetDuration":4,"studyType":22,"phases":207,"briefSummary":209,"conditions":210,"keywords":211,"overallStatus":219,"whyStopped":4,"lastUpdateSubmitDate":220,"lastUpdatePostDateStruct":221,"startDateStruct":223,"completionDateStruct":225,"leadSponsor":227,"locationsCount":4},"100582596","phase-4-preoperative-use-of-liraglutide-additionally-to-common-dietological-measures-as-opposed-to-dietological-measures-alone-100582596","NCT06865365","Preoperative Use of Liraglutide Additionally to Common Dietological Measures as Opposed to Dietological Measures Alone","Prospective, Randomized, Controlled Trial of Preoperative Use of Saxenda (Liraglutide) Additionally to Common Dietological Measures as Opposed to Dietological Measures Alone","Inclusion Criteria:\n\n\\- Patients seeking bariatric surgery\n\n* BMI \\> 35.0 kg\u002Fm2\n* Health insurance via Österreichische Gesundheitskasse\n* Willingness to be assigned to either of the two groups\n* Willingness to adhere to preoperative dietological measures\n* Follow-up anticipation with blood draws and body weight scans using Secca scale\n* Written informed consent\n\nExclusion Criteria:\n\n* Patients with previous bariatric surgerys\n\n  * Patients aged below 18 years\n  * Patients with BMI \\\u003C 35 kg\u002Fm2\n  * Patients with psychiatric disorders\n  * Patients not willing to adhere to preoperative dietological measures\n  * Patients with contraindications against Saxenda\n  * Patients who have health insurance other than Österreichische Gesundheitskasse",{"count":206,"type":21},72,[208],"PHASE4","The aim of the study is to investigate the effects of preoperative Saxenda (liraglutide). There are two groups, one group receives Saxena in addition to dietary measures when first seeking the operation, one group only diet. The investigator is researching how much additional preoperative weight loss is possible with the drug admitted preoperatively.",[27],[140,212,213,214,215,216,217,218],"Bariatric surgery","metabolic surgery","liraglutide","saxenda","weight loss","surgery risk reduction","excess weight loss","NOT_YET_RECRUITING","2025-03-18",{"date":222,"type":34},"2025-03-21",{"date":224,"type":21},"2025-05-01",{"date":226,"type":21},"2028-02-01",{"name":228,"class":41},"Medical University of Vienna",{"id":230,"slug":231,"hasResults":11,"nctId":232,"briefTitle":233,"officialTitle":233,"acronym":234,"eligibilityCriteria":235,"healthyVolunteers":75,"sex":16,"minAge":17,"maxAge":236,"enrollmentInfo":237,"targetDuration":4,"studyType":22,"phases":239,"briefSummary":240,"conditions":241,"keywords":245,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":251,"lastUpdatePostDateStruct":252,"startDateStruct":254,"completionDateStruct":256,"leadSponsor":258,"locationsCount":92},"100502140","wakaya-rising-up-for-choctaw-youth-health-100502140","NCT05818384","Wakaya: Rising Up for Choctaw Youth Health","Wakaya","Inclusion Criteria:\n\n* Be enrolled in Choctaw Nation of Oklahoma (CNO)\n* Live within CNO tribal region for 12 months\n\nYES to one of the following:\n\n* Consumed sweetened beverages or processed\u002Ffast food 2x or more per week; OR\n* Engaged in excessive sitting or lying around (\\>540 min\u002Fday) or engage in small screen recreation (\\>2 hours\u002Fday); OR\n* Physical activity - spend \\\u003C60 minutes\u002Fday outdoors or \\\u003C2.5 hrs per week in moderate or vigorous physical activity OR spend \\\u003C60 minutes a day in moderate or vigorous intensity aerobic activity; OR\n* Engage in any T.V., small screen\u002Fvideo game recreation (\\> 2 hours\u002Fday)\n\nExclusion Criteria:\n\n* opioid\u002Fmethamphetamine drug use (2 times or more in past month)\n* allergic reactions to food (e.g. peanuts), plant (poison oak or ivy) or insects (e.g. bees, fire ants) that caused difficulty in breathing or necessitated hospitalization or caused an anaphylactic reaction\n* disability that prevents student from walking or from engaging in exercise\n* aggressive, violent, combative or inappropriate behaviors\n* inability to follow directions\n* psychotic symptoms","19 Years",{"count":238,"type":21},176,[24],"Investigators will conduct a two-group randomized waitlist-control trial to assess the efficacy of the Wakaya: Rising Up for Choctaw Youth Health program on improving physical activity, reducing sedentary behaviors and improving healthful eating habits as well as delaying or reducing alcohol, tobacco and other drug use. Wakaya is an experiential, outdoor, nature-based program grounded in Choctaw values. It is a multi-level intervention that increases individual motivation and leadership skills to make healthy behavioral choices for behavior and exercise.",[27,242,243,244],"Healthy Nutrition","Sedentary Behavior","Drug Abuse",[246,247,248,249,250],"Native Americans","Youth","Oklahoma","Adolescents","Obesity prevention","2025-02-18",{"date":253,"type":34},"2025-02-20",{"date":255,"type":34},"2023-04-28",{"date":257,"type":21},"2027-04-30",{"name":259,"class":41},"University of Washington",{"id":261,"slug":262,"hasResults":11,"nctId":263,"briefTitle":264,"officialTitle":265,"acronym":4,"eligibilityCriteria":266,"healthyVolunteers":11,"sex":16,"minAge":18,"maxAge":4,"enrollmentInfo":267,"targetDuration":4,"studyType":22,"phases":269,"briefSummary":270,"conditions":271,"keywords":272,"overallStatus":219,"whyStopped":4,"lastUpdateSubmitDate":276,"lastUpdatePostDateStruct":277,"startDateStruct":279,"completionDateStruct":281,"leadSponsor":283,"locationsCount":159},"100580269","phase-2-perioperative-music-in-obese-patients-under-spinal-anesthesia-100580269","NCT06835101","Perioperative Music in Obese Patients Under Spinal Anesthesia","The Effect of Music Versus Midazolam on Perioperative Anxiety of Obese Patients Under Spinal Anesthesia","Inclusion Criteria:\n\n* patients who are \\> 18 years old\n* patients with Body Mass Index -ΒΜΙ\\>30 kg\u002Fm2\n* patients who will give informed consent in receiving spinal anaesthesia\n* patients who will give informed consent in participating in the study\n\nExclusion Criteria:\n\n* absolute contraindications of spinal anaesthesia,\n* severe psychiatric, cognitive or sensory impairment\n* mother language other than greek,\n* known hypersensitivity to midazolam,\n* renal impairment",{"count":268,"type":21},40,[54],"The goal of this clinical trial is to learn whether music or midazolam has a greater anxiolytic effect on obese patients undergoing spinal anesthesia. It will also determine the safety of music compared to midazolam in this population (differences in blood pressure, heart rate, oxygen saturation). The main question to answer: Music or midazolam is more effective in reducing anxiety in obese patients under spinal anesthesia?",[27],[273,274,275],"obese","music","anxiety","2025-02-15",{"date":278,"type":34},"2025-02-19",{"date":280,"type":21},"2025-02",{"date":282,"type":21},"2025-12",{"name":284,"class":285},"Asklepieion Voulas General Hospital","OTHER_GOV",{"id":287,"slug":288,"hasResults":11,"nctId":289,"briefTitle":290,"officialTitle":291,"acronym":292,"eligibilityCriteria":293,"healthyVolunteers":75,"sex":16,"minAge":294,"maxAge":295,"enrollmentInfo":296,"targetDuration":4,"studyType":22,"phases":298,"briefSummary":299,"conditions":300,"keywords":301,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":307,"lastUpdatePostDateStruct":308,"startDateStruct":310,"completionDateStruct":312,"leadSponsor":314,"locationsCount":42},"100555684","nutrition-goes-to-school-a-school-based-nutrition-intervention-to-promote-healthy-eating-behaviour-among-adolescents-100555684","NCT06515288","Nutrition Goes to School: a School-based Nutrition Intervention to Promote Healthy Eating Behaviour Among Adolescents","The Effect of a School-based Nutrition Intervention to Promote Healthy Eating Behaviour Among Adolescents in Indonesia - a Cluster Randomized Pilot Study","ESTEEM-NGTS","Inclusion Criteria:\n\n* High school students in grades 10-11\n* Aged 15-17 years\n* Attending school in Jakarta\n\nExclusion Criteria:\n\n* unwilling and\u002For unable to complete the questionnaire thoroughly","15 Years","17 Years",{"count":297,"type":21},1000,[24],"The goal of this cluster randomized controlled pilot trial is to assess the feasibility and effect of a school-based nutrition intervention program called \"Nutrition Goes to School\" (NGTS) in improving a healthy diet and physical activities as part of the prevention and management of obesity among adolescents in urban Indonesia. The main questions it aims to answer concern the feasibility of the NGTS multi-component school-based nutrition intervention model in selected secondary schools in an urban setting to inform the design of the future effectiveness study. Additionally, it aims to evaluate the effect of the school-based nutrition intervention in the healthy eating knowledge and behavior (fruit and vegetable consumption, energy-dense nutrient poor food, and sugary beverages consumption, as measured by food frequency questionnaire) and physical activities as well as its effect on nutrition status (body mass index, mid-upper arm circumference \\[MUAC\\] and waist circumference). The intervention components consist of nutrition education to school communities (teachers, management, students and parents), healthy school canteen, school garden, hygiene and sanitation promotion of the school environment and obesogenic environment control, and promotion of physical activities among students. Five secondary schools in Jakarta will be randomly assigned to receive the intervention for 6 months, and five other schools will serve as the control group.",[27],[302,303,304,305,306],"School-based intervention","obesity","adolescent","prevention","nutrition","2024-07-22",{"date":309,"type":34},"2024-07-23",{"date":311,"type":34},"2024-01-09",{"date":313,"type":21},"2024-08-31",{"name":315,"class":41},"SEAMEO Regional Centre for Food and Nutrition",{"id":317,"slug":318,"hasResults":11,"nctId":319,"briefTitle":320,"officialTitle":321,"acronym":322,"eligibilityCriteria":323,"healthyVolunteers":11,"sex":16,"minAge":324,"maxAge":325,"enrollmentInfo":326,"targetDuration":4,"studyType":103,"phases":4,"briefSummary":328,"conditions":329,"keywords":332,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":335,"lastUpdatePostDateStruct":336,"startDateStruct":338,"completionDateStruct":340,"leadSponsor":342,"locationsCount":42},"100421362","adolescents-bariatric-surgery-cohort-survey-100421362","NCT04766801","Adolescents Bariatric Surgery Cohort Survey","Evaluation of the Efficiency and Complications Associated With the Surgical Treatment of Obesity by Laparoscopic Adjustable Gastric Banding in an Adolescent Population.","BariAdo","Inclusion Criteria:\n\n* Patients aged 14-20 years of age and asking for bariatric surgery\n* BMI \\>= 40 Kg.m-2 or \\>= 35 Kg.m-2 with major obesity-related comorbidities (hypertension, diabetes, sleep apnea, etc...)\n\nExclusion Criteria:\n\n* An unstable psychiatric disorder\n* Bariatric surgery anesthesic contraindications\n* Having not completed a minimum of six months of the pre operative program\n* Lack of consent from the patient or the patient's relatives.","14 Years","20 Years",{"count":327,"type":21},100,"Obesity affects 3%-4% of the pediatric population and leads to cardiac mortality during adult life. Bariatric surgery is the best treatment for weight loss and preventing obesity associated comorbidities in adults, but its applications and safety are yet to be defined for adolescents.",[330,331,27],"Bariatric Surgery Candidate","Obesity, Morbid",[333,334,216],"gastric banding","complications","2021-02-19",{"date":337,"type":34},"2021-02-23",{"date":339,"type":34},"2008-01-01",{"date":341,"type":21},"2030-12-31",{"name":343,"class":285},"University Hospital, Angers"]