[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100633422":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":31,"centralContacts":35,"locations":40,"responsibleParty":42,"collaborators":44,"id":47,"slug":48,"hasResults":49,"nctId":50,"briefTitle":51,"officialTitle":51,"acronym":25,"eligibilityCriteria":52,"healthyVolunteers":53,"sex":54,"minAge":55,"maxAge":40,"enrollmentInfo":56,"targetDuration":40,"studyType":59,"phases":60,"briefSummary":62,"conditions":63,"keywords":40,"overallStatus":67,"whyStopped":40,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":40},{"fullName":5,"class":6},"Thomas Jefferson University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Improving Dementia Care (IDC)","EXPERIMENTAL","During a phone session, participants receive ADRD Education and Personalized Decision Counseling, which consists of eliciting values and goals to reach informed, preference-based decisions on whether to have an ADRD evaluation. Participants' primary care physicians are sent cognitive screening results and a smart order set (i.e., orders for ADRD-relevant lab and neuroimaging) via the electronic health record (EHR).",[13],"Other: Improving Dementia Care",{"label":15,"type":16,"description":17,"interventionNames":18},"Enhanced Usual Care (EUC)","ACTIVE_COMPARATOR","Usual care enhanced with notices sent to participants' primary care physicians with cognitive screening results and a smart order set (i.e., orders for ADRD-relevant lab and neuroimaging) via the electronic health record (EHR).",[19],"Other: Enhanced Usual Care",[21,26],{"type":6,"name":22,"description":11,"armGroupLabels":23,"otherNames":24},"Improving Dementia Care",[9],[25],"IDC",{"type":6,"name":27,"description":17,"armGroupLabels":28,"otherNames":29},"Enhanced Usual Care",[15],[30],"EUC",[32],{"name":33,"affiliation":5,"role":34},"Barry Rovner, MD","PRINCIPAL_INVESTIGATOR",[36],{"name":37,"role":38,"phone":39,"phoneExt":40,"email":41},"Nina Diamond, MPH","CONTACT","267-872-1302",null,"nina.diamond@jefferosn.edu",{"type":43,"investigatorFullName":40,"investigatorTitle":40,"investigatorAffiliation":40,"oldNameTitle":40,"oldOrganization":40},"SPONSOR",[45],{"name":46,"class":6},"Independence Blue Cross","100633422","improving-dementia-care-in-primary-practice-100633422",false,"NCT07526480","Improving Dementia Care in Primary Practice","Inclusion Criteria:\n\n* No previous diagnosis of mild cognitive impairment (MCI) or Alzheimer's disease (AD).\n* Have a scheduled PCP visit in the next 4-6 weeks\n* Have subjective cognitive impairment\n* Score ≥ 26 on the Telephone Interview for Cognitive Status (TICS)\n\nExclusion Criteria:\n\n* EHR evidence or previous cognitive evaluations, diagnosis of MCI or AD, or use of AD medications\n* TICS score of ≤ 11.00\n* Inability to provide informed consent",true,"ALL","66 Years",{"count":57,"type":58},80,"ESTIMATED","INTERVENTIONAL",[61],"NA","This clinical trial will evaluate a multi-level scalable intervention called Improving Dementia Care (IDC). The investigators hypothesize that IDC will increase dementia detection in patients with impaired cognition more than the control condition, Enhanced Usual Care (EUC), over 6 months.",[64,65,66],"Alzheimer Disease (AD)","Mild Cognitive Impairment (MCI)","Dementia","NOT_YET_RECRUITING","2026-04-14",{"date":70,"type":71},"2026-04-17","ACTUAL",{"date":73,"type":58},"2026-05-04",{"date":75,"type":58},"2027-05-03",{"name":5,"class":6}]