Video program eases burden for FTD caregivers
NCT ID NCT05338710
First seen Jan 04, 2026 · Last updated Jun 21, 2026 · Updated 23 times
Summary
This study tested a video-based program called STELLA-FTD to help family caregivers of people with frontotemporal dementia (FTD). Sixteen caregivers participated in the program, which aimed to reduce their stress and improve their quality of life. The approach used videoconferencing to deliver support and education tailored to the unique challenges of FTD caregiving.
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This is a summary of
the original study
.
Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Contacts and locations
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Locations
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Oregon Health and Science University, Layton Aging and Alzheimer's Disease Center
Portland, Oregon, 97239, United States
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
Active substance
STELLA-FTD behavioral intervention
What this could lead to
If successful, this program could provide a practical, home-based way to reduce caregiver burnout and improve well-being for families facing FTD.
What could go wrong
This was a small, completed study with only 16 participants, so results may not apply to all caregivers. The intervention is supportive, not a treatment for the disease itself.
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.