[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100557772":3},{"organization":4,"armGroups":7,"interventions":16,"overallOfficials":10,"centralContacts":30,"locations":36,"responsibleParty":50,"collaborators":10,"id":54,"slug":55,"hasResults":56,"nctId":57,"briefTitle":58,"officialTitle":59,"acronym":10,"eligibilityCriteria":60,"healthyVolunteers":56,"sex":61,"minAge":62,"maxAge":10,"enrollmentInfo":63,"targetDuration":66,"studyType":67,"phases":10,"briefSummary":68,"conditions":69,"keywords":10,"overallStatus":72,"whyStopped":10,"lastUpdateSubmitDate":73,"lastUpdatePostDateStruct":74,"startDateStruct":77,"completionDateStruct":79,"leadSponsor":81,"locationsCount":82},{"fullName":5,"class":6},"Ohio State University","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Study Population",null,"Adults ages 50 years and older who are fluent in English and are diagnosed with subjective cognitive concerns (SCD) or objective cognitive decline with mostly intact functioning (MCI diagnosis) as part of clinical work up",[13,14,15],"Behavioral: Assessments","Other: Neuroimaging volumetric measures","Other: Biofluid samples",[17,22,26],{"type":18,"name":19,"description":20,"armGroupLabels":21,"otherNames":10},"BEHAVIORAL","Assessments","Participants will undergo a standard battery of neuropsychological measures, behavioral questionnaire, and functional assessment to monitor cognition and function over time. Clinical data obtained as part of standard of care will be collected from the medical record",[9],{"type":6,"name":23,"description":24,"armGroupLabels":25,"otherNames":10},"Neuroimaging volumetric measures","Neuroimaging volumetric measures will be obtained from already conducted standard of care neuroimaging.",[9],{"type":6,"name":27,"description":28,"armGroupLabels":29,"otherNames":10},"Biofluid samples","Biofluid sampling data will be obtained through another protocol. All participants will be required to sign that consent to participate in this trial.",[9],[31],{"name":32,"role":33,"phone":34,"phoneExt":10,"email":35},"Jessica Pommy, PhD","CONTACT","614-293-4969","jessica.pommy@osumc.edu",[37],{"facility":38,"status":10,"city":39,"state":40,"zip":41,"country":42,"countryCode":43,"cosmosGeoPoint":44,"geoPoint":49,"contacts":10},"The Ohio State University","Columbus","Ohio","43210","United States","US",{"type":45,"coordinates":46},"Point",[47,48],-82.99879,39.96118,{"lat":48,"lon":47},{"type":51,"investigatorFullName":52,"investigatorTitle":53,"investigatorAffiliation":5,"oldNameTitle":10,"oldOrganization":10},"PRINCIPAL_INVESTIGATOR","Douglas Scharre","Professor-Clinical","100557772","under-represented-communities-diagnosed-with-scd-or-mci-through-tele-cog-100557772",false,"NCT06542458","Under-Represented Communities Diagnosed With SCD or MCI Through Tele-Cog","A Cohort Study of Older Adults From Under-resourced\u002FUnder-represented Communities Diagnosed With Subjective Cognitive Decline (SCD) or Mild Cognitive Disorder (MCI) Through Standard of Care Tele-Cog Visits (Tele-Cog)","Inclusion Criteria:\n\n1. Adults ages 50 years and older\n2. Diagnosed with subjective cognitive concerns (SCD) or objective cognitive decline with mostly intact functioning (MCI diagnosis) as part of clinical work up\n3. Fluent in English\n4. Able to provide voluntary informed consent\n5. Willing and able to undergo all study procedures\n6. Able to delegate, if possible, a study partner to contribute information regarding daily activities and cognition\n\nExclusion Criteria:\n\n1. Diagnosis of dementia at baseline.\n2. Inability to give informed consent.\n3. High risk of adverse emotional or behavioral reaction based on investigator's clinical evaluation (e.g., evidence of serious personality disorder, antisocial behavior, serious current stressors, lack of meaningful social support).","ALL","50 Years",{"count":64,"type":65},1000,"ESTIMATED","5 Years","OBSERVATIONAL","Overall, this study's primary aim is to establish a prospective, longitudinal, observational cohort study of older adults at risk for dementia from under-resourced\u002Funderrepresented communities. More specifically, older adults diagnosed with subjective cognitive decline (SCD) or Mild Cognitive Impairment (MCI) during clinical care offered via the Tele-Cog clinic would be recruited for more comprehensive data collection to characterize the clinical presentation and course of illness over multiple timepoints spread out longitudinally.",[70,71],"Mild Cognitive Impairment","Subjective Cognitive Decline","NOT_YET_RECRUITING","2026-02-23",{"date":75,"type":76},"2026-02-25","ACTUAL",{"date":78,"type":65},"2026-12-01",{"date":80,"type":65},"2032-01-01",{"name":5,"class":6},1]