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

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
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 video-conference 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 US.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 100
Healthy Volunteers: t
View:

• 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

• 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

Locations
United States
Oregon
Oregon Health & Science University
RECRUITING
Portland
Contact Information
Primary
Hailey Chatterton, MS
chatterton@ohsu.edu
503-568-9725
Backup
Allison Lindauer, PhD, APRN
lindauer@ohsu.edu
503-494-6976
Time Frame
Start Date: 2025-06-23
Estimated Completion Date: 2029-06
Participants
Target number of participants: 640
Treatments
Active_comparator: Control Group
Control group, receives information and support in a group setting (N=160 Care Partners).
Experimental: Test Group
Test group, receives information and support in a group setting, but program is different from control (N=160 Care Partners).
No_intervention: Care Recipients with FTD
Care recipients are consented to inform them of their rights, but they do not take part in any activities (N=320 Care Recipients).
Related Therapeutic Areas
Sponsors
Collaborators: National Institute on Aging (NIA)
Leads: Oregon Health and Science University

This content was sourced from clinicaltrials.gov

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