[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100611901":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":25,"centralContacts":32,"locations":41,"responsibleParty":55,"collaborators":57,"id":61,"slug":62,"hasResults":63,"nctId":64,"briefTitle":65,"officialTitle":65,"acronym":66,"eligibilityCriteria":67,"healthyVolunteers":68,"sex":69,"minAge":70,"maxAge":71,"enrollmentInfo":72,"targetDuration":18,"studyType":75,"phases":76,"briefSummary":78,"conditions":79,"keywords":82,"overallStatus":84,"whyStopped":18,"lastUpdateSubmitDate":85,"lastUpdatePostDateStruct":86,"startDateStruct":89,"completionDateStruct":91,"leadSponsor":93,"locationsCount":94},{"fullName":5,"class":6},"Virginia Commonwealth University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Virtual Housecalls Intervention (VHC)","EXPERIMENTAL","Includes standard in-person pediatric primary care, 6 months of telehealth sessions with a behavior coach (3 months with weekly sessions, 3 months with bi-weekly sessions), and weekly exercise videos sent electronically for the 6 month intervention. Sessions include real-time skill building that uses items or space in families' home to tailor the treatment and personalize content application to their context.",[13],"Behavioral: Virtual Housecalls",{"label":15,"type":16,"description":17,"interventionNames":18},"Enhanced Treatment as Usual (TAU+)","NO_INTERVENTION","Includes standard in-person pediatric primary care, enhanced with PPCP training on obesity treatment guidelines and publicly available education regarding healthy eating and exercise, delivered to participants on a contact schedule matched to the intervention group.",null,[20],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":18},"BEHAVIORAL","Virtual Housecalls","26 contact hours of evidence-based intensive health and behavioral lifestyle treatment, as per the American Academy of Pediatrics Clinical Practice Guidelines",[9],[26,29],{"name":27,"affiliation":5,"role":28},"Melanie K Bean, PhD","PRINCIPAL_INVESTIGATOR",{"name":30,"affiliation":31,"role":28},"Shari Barkin, PhD","Emory University",[33,38],{"name":34,"role":35,"phone":36,"phoneExt":18,"email":37},"Sarah M Farthing, MS","CONTACT","804-527-4756","sarah.malone@vcuhealth.org",{"name":27,"role":35,"phone":39,"phoneExt":18,"email":40},"804-527-4765","melanie.bean@vcuhealth.org",[42],{"facility":43,"status":18,"city":44,"state":45,"zip":46,"country":47,"countryCode":48,"cosmosGeoPoint":49,"geoPoint":54,"contacts":18},"Children's Hospital of Richmond at VCU Healthy Lifestyles Center","Henrico","Virginia","23239","United States","US",{"type":50,"coordinates":51},"Point",[52,53],-78.61611,36.59264,{"lat":53,"lon":52},{"type":56,"investigatorFullName":18,"investigatorTitle":18,"investigatorAffiliation":18,"oldNameTitle":18,"oldOrganization":18},"SPONSOR",[58],{"name":59,"class":60},"National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)","NIH","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":73,"type":74},500,"ESTIMATED","INTERVENTIONAL",[77],"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.",[80,81],"Class I Obesity","Pediatric Obesity",[83],"Lifestyle Intervention","NOT_YET_RECRUITING","2026-05-30",{"date":87,"type":88},"2026-06-02","ACTUAL",{"date":90,"type":74},"2026-07-01",{"date":92,"type":74},"2030-01-31",{"name":5,"class":6},1]