[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100573218":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":32,"centralContacts":33,"locations":43,"responsibleParty":89,"collaborators":91,"id":97,"slug":98,"hasResults":99,"nctId":100,"briefTitle":101,"officialTitle":102,"acronym":103,"eligibilityCriteria":104,"healthyVolunteers":105,"sex":106,"minAge":107,"maxAge":108,"enrollmentInfo":109,"targetDuration":32,"studyType":112,"phases":113,"briefSummary":115,"conditions":116,"keywords":119,"overallStatus":46,"whyStopped":32,"lastUpdateSubmitDate":123,"lastUpdatePostDateStruct":124,"startDateStruct":127,"completionDateStruct":129,"leadSponsor":131,"locationsCount":132},{"fullName":5,"class":6},"IDeA States Pediatric Clinical Trials Network","NETWORK",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"RAMP Reports","EXPERIMENTAL","Submit RAMP reports weekly for 4 weeks and then monthly for 2 months.",[13],"Other: RAMP Reports",{"label":15,"type":16,"description":17,"interventionNames":18},"Digital Education Handouts","ACTIVE_COMPARATOR","Standard of care determined by the treating healthcare provider and digital education handouts (attention controls) distributed by the study team weekly for 4 weeks and then monthly for 2 months.",[19],"Other: Digital Education Handouts",[21,27],{"type":22,"name":9,"description":23,"armGroupLabels":24,"otherNames":25},"OTHER","Participants will receive text-based requests for reports with embedded links to select radio button questionnaires directly on their mobile device. Questions include current inattention\u002Fhyperactivity symptoms, school performance, and any engagement in behavioral therapy. Inattention\u002Fhyperactivity symptom questions and scoring is taken directly from the publicly available Vanderbilt Rating Scales, which is a commonly used, guideline-recommended tool for both diagnosis and management of ADHD for use by parents and teachers.",[9],[26],"Remote ADHD Monitoring Program",{"type":22,"name":15,"description":28,"armGroupLabels":29,"otherNames":30},"The digital education handouts will be sent via email to the control group and will serve as an attention control. They will consist of information regarding a general pediatric health topic and will be emailed at intervals matching the RAMP requests in the intervention group.",[15],[31],"Standard of Care",null,[34,39],{"name":35,"role":36,"phone":37,"phoneExt":32,"email":38},"Song Ounpraseuth, PhD","CONTACT","501-686-7233","STOunpraseuth@uams.edu",{"name":40,"role":36,"phone":41,"phoneExt":32,"email":42},"Kripa Patel, BDS, MPH","(501) 686-5547","kpatel@uams.edu",[44,69],{"facility":45,"status":46,"city":47,"state":48,"zip":49,"country":50,"countryCode":51,"cosmosGeoPoint":52,"geoPoint":57,"contacts":58},"University of Mississippi Medical Center","RECRUITING","Jackson","Mississippi","39216","United States","US",{"type":53,"coordinates":54},"Point",[55,56],-90.18481,32.29876,{"lat":56,"lon":55},[59,63,67],{"name":60,"role":36,"phone":61,"phoneExt":32,"email":62},"Hannah Ford, PhD","601-815-8413","hford@umc.edu",{"name":64,"role":36,"phone":65,"phoneExt":32,"email":66},"Lacy Malloch, BS","601-815-4517","lmalloch@umc.edu",{"name":60,"role":68,"phone":32,"phoneExt":32,"email":32},"PRINCIPAL_INVESTIGATOR",{"facility":70,"status":46,"city":71,"state":72,"zip":73,"country":50,"countryCode":51,"cosmosGeoPoint":74,"geoPoint":78,"contacts":79},"Medical University of South Carolina","Charleston","South Carolina","29425",{"type":53,"coordinates":75},[76,77],-79.93275,32.77632,{"lat":77,"lon":76},[80,84,88],{"name":81,"role":36,"phone":82,"phoneExt":32,"email":83},"Claire MacGeorge, MD","843-876-8512","macgeorg@musc.edu",{"name":85,"role":36,"phone":86,"phoneExt":32,"email":87},"Shannon Cabaniss, BA","843-732-1839","smw207@musc.edu",{"name":81,"role":68,"phone":32,"phoneExt":32,"email":32},{"type":90,"investigatorFullName":32,"investigatorTitle":32,"investigatorAffiliation":32,"oldNameTitle":32,"oldOrganization":32},"SPONSOR",[92,93,94],{"name":70,"class":22},{"name":45,"class":22},{"name":95,"class":96},"National Institutes of Health (NIH)","NIH","100573218","a-pilot-study-of-a-remote-adhd-monitoring-program-100573218",false,"NCT06743425","A Pilot Study of a Remote ADHD Monitoring Program","A Pilot Study of a Remote Attention-Deficit\u002FHyperactivity Disorder Monitoring Program (RAMP) for Children in Rural Areas","RAMP","Inclusion Criteria:\n\nThe child must\n\n* be under the care of a participating provider\n* be aged 5-11 at enrollment\n* have a diagnosis of ADHD\n* be initiating stimulant medication for treatment for the first time or have not received stimulant medication for the last 6 months\n* be attending in-person elementary school\n\nThe Primary caregiver must\n\n* be willing and legally able to give consent\n* have access to a smartphone\n* be English-speaking\n* reside with the child at least 3 days per week\n* complete an initial symptom assessment prior to starting stimulant treatment and be willing to provide a copy to the study team\n\nThe provider must\n\n* manage ADHD care in patients age 5-11 years\n* provide informed consent\n* agree to use the RAMP platform if they care for patients randomized to use it\n* agree to provide information to potential participants about the study and contact the research coordinator if interested\n\nExclusion Criteria:\n\nChild:\n\n* has serious mental health comorbidities (Children with depression, anxiety, oppositional defiant disorder will be permitted to participate. Children with schizophrenia, bipolar disorder, conduct disorder and those who have been hospitalized for any mental health condition will be excluded from the study.)\n* has severe neurodevelopment disorders (Children with well-controlled seizure disorders will be permitted to participate.)\n* is currently receiving, or previously received, atypical antipsychotic medication treatment\n* is or becomes pregnant",true,"ALL","5 Years","11 Years",{"count":110,"type":111},36,"ESTIMATED","INTERVENTIONAL",[114],"NA","RAMP is a pilot study examining the use of an Attention-Deficit\u002FHyperactivity Disorder (ADHD) Monitoring Program during the early stages of treating ADHD in children living in rural settings. This trial will enroll 36 caregiver\u002Finfant dyads across 2 sites and will evaluate feasibility endpoints rather than clinical outcomes. Enrolled participants will be randomized 1:1 to the intervention group (RAMP reports) or control group (digital education handouts). The study duration is 10 months, including start-up, enrollment and intervention, and data analysis and manuscript submission.",[117,118],"Attention-deficit\u002FHyperactivity Disorder","ADHD",[120,121,122],"Rural health","Vanderbilt","Text-based Symptom Reporting","2026-04-27",{"date":125,"type":126},"2026-04-28","ACTUAL",{"date":128,"type":126},"2025-02-04",{"date":130,"type":111},"2026-07-01",{"name":5,"class":6},2]