[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100563210":3},{"organization":4,"armGroups":7,"interventions":25,"overallOfficials":35,"centralContacts":42,"locations":51,"responsibleParty":68,"collaborators":71,"id":75,"slug":76,"hasResults":77,"nctId":78,"briefTitle":79,"officialTitle":79,"acronym":80,"eligibilityCriteria":81,"healthyVolunteers":82,"sex":83,"minAge":84,"maxAge":85,"enrollmentInfo":86,"targetDuration":24,"studyType":89,"phases":90,"briefSummary":92,"conditions":93,"keywords":98,"overallStatus":54,"whyStopped":24,"lastUpdateSubmitDate":101,"lastUpdatePostDateStruct":102,"startDateStruct":105,"completionDateStruct":107,"leadSponsor":109,"locationsCount":110},{"fullName":5,"class":6},"Oregon Health and Science University","OTHER",[8,14,20],{"label":9,"type":10,"description":11,"interventionNames":12},"Control Group","ACTIVE_COMPARATOR","Control group, receives information and support in a group setting (N=160 Care Partners).",[13],"Behavioral: STELLA-FTD Control",{"label":15,"type":16,"description":17,"interventionNames":18},"Test Group","EXPERIMENTAL","Test group, receives information and support in a group setting, but program is different from control (N=160 Care Partners).",[19],"Behavioral: STELLA-FTD Test",{"label":21,"type":22,"description":23,"interventionNames":24},"Care Recipients with FTD","NO_INTERVENTION","Care recipients are consented to inform them of their rights, but they do not take part in any activities (N=320 Care Recipients).",null,[26,31],{"type":27,"name":28,"description":29,"armGroupLabels":30,"otherNames":24},"BEHAVIORAL","STELLA-FTD Control","Participants receive information about FTD and support via weekly group video-conference-based meetings.",[9],{"type":27,"name":32,"description":33,"armGroupLabels":34,"otherNames":24},"STELLA-FTD Test","The test group receives a information and support, but with a focus that is different from the Control Group",[15],[36,39],{"name":37,"affiliation":5,"role":38},"Allison Lindauer, PhD, APRN","PRINCIPAL_INVESTIGATOR",{"name":40,"affiliation":5,"role":41},"Aimee Mooney, MA, CCC-SLP","STUDY_DIRECTOR",[43,48],{"name":44,"role":45,"phone":46,"phoneExt":24,"email":47},"Hailey Chatterton, MS","CONTACT","503-568-9725","chatterton@ohsu.edu",{"name":37,"role":45,"phone":49,"phoneExt":24,"email":50},"503-494-6976","lindauer@ohsu.edu",[52],{"facility":53,"status":54,"city":55,"state":56,"zip":57,"country":58,"countryCode":59,"cosmosGeoPoint":60,"geoPoint":65,"contacts":66},"Oregon Health & Science University","RECRUITING","Portland","Oregon","97239","United States","US",{"type":61,"coordinates":62},"Point",[63,64],-122.67621,45.52345,{"lat":64,"lon":63},[67],{"name":44,"role":45,"phone":46,"phoneExt":24,"email":47},{"type":38,"investigatorFullName":69,"investigatorTitle":70,"investigatorAffiliation":5,"oldNameTitle":24,"oldOrganization":24},"Allison Lindauer","Associate Professor",[72],{"name":73,"class":74},"National Institute on Aging (NIA)","NIH","100563210","stella-ftd-examination-of-a-behavior-change-intervention-for-ftd-family-care-partners-100563210",false,"NCT06613204","STELLA-FTD: Examination of a Behavior Change Intervention for FTD Family Care Partners","STELLA-FTD","Inclusion Criteria: Family Care Partner\n\n* Adult caring for family member with FTD.\n* Provides 4 or more hours of care\u002Fweek. Does not have to reside with.\n* Identifies at least 2 moderately upsetting behaviors in the person with FTD.\n* Speaks and understands English to be able to participate in intervention.\n* Owns a telephone (smartphone, cell phone or landline).\n* Has email and mailing address to receive computer, study materials and surveys.\n* Provides informed consent to participate in the research.\n* Lives in the US\n\nInclusion Criteria: Person with FTD\n\n* Diagnosis of FTD\n* Family member of a Care Partner (this can be a relative, spouse, or close kin that is considered family).\n* Lives in US\n\nExclusion Criteria: Person with FTD\n\n* No Frontotemporal Degeneration diagnosis.\n* Unable to leave Care Partner during STELLA-FTD sessions.\n* Enrolled in hospice.\n\nExclusion Criteria: Family Care Partner\n\n* Unable to find activity for Care Recipient during STELLA-FTD sessions to allow Care Partner to work privately with Guide and other Care Partners.\n* Hearing and\u002For vision problems severe enough to prevent participation.\n* Refuses to be video-recorded during STELLA-FTD sessions.\n* Unwilling or unable to adequately follow study instructions and participate in study procedures.",true,"ALL","18 Years","100 Years",{"count":87,"type":88},640,"ESTIMATED","INTERVENTIONAL",[91],"NA","The purpose of this nationwide study is to test STELLA-FTD (Support via Telehealth: Living and Learning with Advancing Alzheimer's Disease)-FTD, an intervention to specifically address the needs of family Care Partners of persons with frontotemporal degeneration (FTD). STELLA-FTD is a multicomponent videoconference-based intervention designed to facilitate effective use of community and peer resources to foster effective management of behavioral and psychological symptoms of dementia. The study is recruiting families from across the United States.",[94,95,96,97],"Frontotemporal Dementia","Caregiver Burden","Primary Progressive Aphasia (PPA)","Corticobasal Syndrome",[99,100],"behavioral intervention","FTD","2025-10-23",{"date":103,"type":104},"2025-10-27","ACTUAL",{"date":106,"type":104},"2025-06-23",{"date":108,"type":88},"2029-06",{"name":5,"class":6},1]