Can a video chat program ease the burden of Alzheimer's caregiving?
NCT ID NCT04627662
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested a video-based program called Tele-STELLA for family members caring for someone with moderate to late-stage Alzheimer's or related dementia. The program connects caregivers with a guide to find ways to manage upsetting behaviors. The goal was to see if it could reduce caregiver stress and improve their well-being. 375 caregivers took part in the completed study.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Tele-STELLA (a video-based behavioral support program for care partners)
- What this could lead to
- If successful, this could provide a practical, home-based tool to help family caregivers reduce distressing dementia behaviors and their own burden.
- What could go wrong
- This is a completed study, not a treatment for Alzheimer's itself. The intervention focuses on caregiver support, not on slowing or curing the disease. Results may not apply to all caregiving situations.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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375 people
The number who actually took part.
- Started
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May 2021
- Finished
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Jul 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Care Recipient Inclusion Criteria: * Diagnosis of ADRD, moderate to late stages as defined by family member (Box 1) * Exhibits 2 or more behaviors listed on RMBPC that are bothersome to the Care Partner and occur 3 or more times/week at study enrollment * Family member of Care Partner (this can be a relative, spouse or close kin that is considered family) Care Recipient Exclusion Criteria: * Dementia not related to ADRD * Unable to leave Care Partner during Tele-STELLA sessions * Early stage dementia, as defined by family member Care Partner Inclusion Criteria: * Adult caring for family member with ADRD * Provides care for at least 4 hours/week * Age of 18 years or older * Speaks and understands English to be able to participate in intervention * Owns a telephone (smartphone, cell phone or landline) * Has mailing address to receive computer and study materials * Provides informed consent to participate in the Research Care Partner Exclusion Criteria: * Unable to find activity for care recipient during Tele-STELLA sessions to allow Care Partner to work privately with Guide and other Care Partners. * Completed similar telehealth intervention within the last year * Hearing and/or vision problems severe enough to prevent participation * Unwilling or unable to adequately follow study instructions and participate in study procedures
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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.
Contacts and locations
Locations
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Oregon Health and Science University, Layton Aging and Alzheimer's Disease Center
Portland, Oregon, 97239, United States
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