Can Home-Based palliative care ease dementia suffering?
NCT ID NCT05749146
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether a team of doctors, nurses, social workers, and community health workers providing palliative care at home can improve symptom control and reduce hospital visits for people with advanced dementia. About 153 patients and their family caregivers are taking part across four hospitals in New York City. The goal is to see if this approach leads to better symptom management and fewer hospital stays.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Home palliative care (behavioral intervention by an interdisciplinary team)
- What this could lead to
- If it works, this could provide a better way to manage symptoms and improve quality of life for dementia patients at home, while also supporting their caregivers.
- What could go wrong
- This is a relatively small trial (153 participants) and focuses on symptom management, not a cure. Results may not apply to all dementia patients or settings.
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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153 people
The number who actually took part.
- Started
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Jun 2023
- Expected to finish
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Aug 2027
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.
- Ages
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65 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.
Inclusion Criteria: * have advanced dementia, based on Global Deterioration Score (GDS)\>6 * impairment in at least one activity of daily living (ADL -which is inherent in this level of GDS) * at least one hospitalization or ED visit within the last 12 months * a physician who is primarily responsible for their dementia-related care whose clinical outpatient site is associated with one of the four Mount Sinai sites in Manhattan * a family caregiver willing to enroll * a residence in Manhattan where they are currently living (not in a long-term care facility) * capacity to consent or a legal representative available to provide consent * fluency in English or Spanish, or their legal representative must be fluent in English or Spanish * age \>64. Exclusion Criteria: * Does not have a family caregiver to enroll * Does not reside in Manhattan outside of long-term care facility * Does not have fluency in English or Spanish Doesn't
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Genom att skicka in godkänner du våra Användarvillkor
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
-
Ichan School of Medicine at Mount Sinai
New York, New York, 10029, United States
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