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Recruiting NCT06613204

STELLA-FTD: Examination of a Behavior Change Intervention for FTD Family Care Partners

Trial Parameters

Condition Frontotemporal Dementia
Sponsor Oregon Health and Science University
Study Type INTERVENTIONAL
Phase N/A
Enrollment 640
Sex ALL
Min Age 18 Years
Max Age 100 Years
Start Date 2025-06-23
Completion 2029-06
Interventions
STELLA-FTD ControlSTELLA-FTD Test

Brief Summary

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.

Eligibility Criteria

Inclusion Criteria: Family Care Partner * Adult caring for family member with FTD. * Provides 4 or more hours of care/week. Does not have to reside with. * Identifies at least 2 moderately upsetting behaviors in the person with FTD. * Speaks and understands English to be able to participate in intervention. * Owns a telephone (smartphone, cell phone or landline). * Has email and mailing address to receive computer, study materials and surveys. * Provides informed consent to participate in the research. * Lives in the US Inclusion Criteria: Person with FTD * Diagnosis of FTD * Family member of a Care Partner (this can be a relative, spouse, or close kin that is considered family). * Lives in US Exclusion Criteria: Person with FTD * No Frontotemporal Degeneration diagnosis. * Unable to leave Care Partner during STELLA-FTD sessions. * Enrolled in hospice. Exclusion Criteria: Family Care Partner * Unable to find activity for Care Recipient during STELLA-FTD sessions to allow Care Partner t

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