[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"class-i-obesity\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:class-i-obesity":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,45],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":30,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100611901","virtual-housecalls-redesigning-pediatric-primary-care-adolescent-obesity-treatment-100611901",false,"NCT07246603","Virtual Housecalls: Redesigning Pediatric Primary Care Adolescent Obesity Treatment","VHC","Adolescent Inclusion Criteria:\n\n* English or Spanish-speaking\n* 12-15 years of age\n* Receiving care at a participating clinic\n* Body Mass Index (BMI) ≥95% and \\\u003C120% of the 95%\n* Access to a mobile device with a webcam that can receive texts\n\nParent Inclusion Criteria:\n\n* English or Spanish-speaking\n* Primary legal guardian ≥18 years of age living with the adolescent\n\nExclusion Criteria:\n\n* conflicts that would inhibit the ability to participate in all aspects of the study as outlined in the study protocol\n* family plans to move outside of the study area or plans to no longer be a patient at a participating clinic in the 12 month study period\n* the primary care provider or PI determines that the study is not clinically or medically appropriate (e.g., significant psychiatric, cognitive, physical or developmental conditions that would impair their ability to complete assessments, participate in study sessions, or conduct physical activity) based on screening at study onset\n* adolescent exhibits severe dietary restriction or compensatory behavior (e.g., vomiting, laxative abuse) based on screening at study onset and clinical interview by a study psychologist\n* adolescent is currently pregnant\u002Fplans to become pregnant during study period\n* adolescent is participating in another weight loss program, has had or plans to undergo weight loss surgery\n* adolescent has a chronic medical condition(s) and\u002For uses medication that substantially impacts or interferes with growth, appetite, weight or physical activity participation\n* adolescents taking anti-obesity medication are ineligible if they are not a stable dose for at least 3 months prior to study participation",true,"ALL","12 Years","15 Years",{"count":21,"type":22},500,"ESTIMATED","INTERVENTIONAL",[25],"NA","This pragmatic randomized clinical trial tests a novel intensive health behavior and lifestyle intervention, conducted via telehealth, to treat class I adolescent obesity in pediatric primary care. Results will inform scalable approaches that meet the recommended treatment dose and effectively treat obesity in this setting.",[28,29],"Class I Obesity","Pediatric Obesity",[31],"Lifestyle Intervention","NOT_YET_RECRUITING","2026-05-30",{"date":35,"type":36},"2026-06-02","ACTUAL",{"date":38,"type":22},"2026-07-01",{"date":40,"type":22},"2030-01-31",{"name":42,"class":43},"Virginia Commonwealth University","OTHER",1,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":49,"acronym":4,"eligibilityCriteria":50,"healthyVolunteers":11,"sex":51,"minAge":52,"maxAge":53,"enrollmentInfo":54,"targetDuration":4,"studyType":23,"phases":56,"briefSummary":57,"conditions":58,"keywords":60,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":44},"100577500","effect-of-pyramidal-training-on-epicardial-fat-for-coronary-artery-disease-prevention-100577500","NCT06799104","EFFECT OF PYRAMIDAL TRAINING ON EPICARDIAL FAT FOR CORONARY ARTERY DISEASE PREVENTION","Inclusion Criteria:\n\n* Fifty females' patients with class I obesity (BMI 30 to 34.9 kg\u002Fm2, Waist circumference \\> 88 cm).\n\n  * Their age ranges from 30-40 years old.\n  * Dyslipidemia and lipid profile as follow (total cholesterol high: 240 mg\u002Fdl, HDL less than 40 mg\u002Fdl, LDL high: 160-189 mg\u002FdL and triglycerides high: 200-499 mg\u002Fdl).\n  * All patients will be clinically and medically stable when attending the study.\n\nExclusion Criteria:\n\n* Patients with conditions will be excluded such as:\n\n  * Musculoskeletal problems.\n  * Chronic pulmonary disease.\n  * Missed more than two weeks of the program or want to terminate the program.\n  * Unstable angina.\n  * Acute illness.\n  * Uncontrolled cardiac arrhythmia.\n  * Decompensated heart failure.\n  * Cognitive impairment or mental disorders.\n  * Systolic blood pressure higher than 180, and\u002For diastolic blood pressure over 100mmHg.\n  * DVT.\n  * Multiple food allergies\u002Fintolerances or gastrointestinal difficulties of the prescribed diet.\n  * Cancer (have special nutritional and training needs).","FEMALE","30 Years","40 Years",{"count":55,"type":22},50,[25],"To show the effect of pyramidal training for coronary artery disease prevention on:\n\n-Epicardial fat, BMI, Waist circumference (WC), Lipid profile, Quality of life and Mediterranean Diet Adherence.",[59,28],"Coronary Artery Disease",[61],"Pyramidal Training, Epicardial Fat,Coronary artery disease.","2025-02-04",{"date":64,"type":36},"2025-02-06",{"date":66,"type":22},"2025-02",{"date":68,"type":22},"2026-01",{"name":70,"class":43},"Cairo University"]