Smart home tech could spot early dementia signs
NCT ID NCT06704971
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This Stanford study is testing whether non-intrusive sensors placed in the home can automatically track neuropsychiatric symptoms like mood changes and agitation in older adults. Researchers will enroll 25 participants with or at risk of mild cognitive impairment or dementia, along with healthy controls. The goal is to create a dashboard for doctors that summarizes symptom patterns, making it easier to diagnose and manage mental health conditions.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- non-intrusive ambient intelligence technologies (in-home video and audio sensors)
- What this could lead to
- If successful, this could lead to a system that helps doctors monitor mental health symptoms at home, potentially catching early signs of dementia or cognitive decline.
- What could go wrong
- This is a small, early-stage study with only 25 participants. The technology may not work as expected in real-world homes, and privacy concerns could limit adoption.
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.
- Participants
-
About 25 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Oct 2024
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- 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.
Who is studied
Older Adults - 65+
- Ages
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65 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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.
Inclusion criteria: * Age 65+ years old * Any age and ethnicity. * With or without, or at risk of mild to moderate dementia and healthy controls. * Availability of a study partner (informant) who has contact with the patient at least once a week (this can also be the surrogate/LAR but does not necessarily have to be) Exclusion criteria: * Those with severe mobility impairments * participants in non-home settings (skilled nursing facilities, etc.).
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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
-
Clinical Excellence Research Center
Palo Alto, California, 94304, United States
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