Zoom therapy eases dementia symptoms at home, study finds
NCT ID NCT05722743
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested an 8-week telehealth program for people with Alzheimer's or related dementias living at home with a caregiver. The program used Zoom to teach caregivers how to improve daily activities and reduce challenging behaviors. 84 people (person with dementia and their caregiver) took part, and the goal was to see if the program was practical and helpful.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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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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84 people
The number who actually took part.
- Started
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Jun 2023
- Finished
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Jun 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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21 to 99 years
- 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: Participants with Dementia * Men or women aged 60-99, inclusive. * Living at home in the community with one primary caregiver. * Diagnosis or probably diagnosis of dementia (confirmed by Clinical Dementia Rating Scale score of 1.0+) * If on psychotropic medication, they are at a point where dosage and treatment are stabilized for the duration of the study. * Functional sensory abilities with or without aids (hearing, vision, smell, touch, taste) * Caregiver report of challenges related to behaviors within 4 weeks of study enrollment. * Caregiver willing to participate throughout duration of study. * Contact with University of Kentucky Alzheimer's Disease Research Center or Kentucky Neuroscience Institute medical provider within 12 months of study recruitment. Inclusion Criteria: Caregiver for Participants with Dementia * Men or women aged 21-99, inclusive. * Willingness to participate in study and implement recommended data collection tools. * English speaking, able to read and write. * Ability to retrieve and send mail. Exclusion Criteria: Participants with Dementia * Unstable medical conditions within one month prior to screening visit such as poorly controlled blood pressure, diabetes, current cancer diagnosis, or breathing problems, etc. * Wheelchair or bed bound. * Residence in skilled nursing facility or facility-based care. * Caregiver report of physically violent behaviors. * Initiation of antipsychotic medication within 4 weeks prior to screening or unpredictable use of such medications * Diagnosis of profound or total sensory altering disorders including macular degeneration, legal blindness, total deafness, severe peripheral neuropathy, anosmia. * Major depression in past 12 months (DSM-IV criteria), major mental illness such as schizophrenia, bipolar disorder, personality disorders, or recent (in past 12 months) alcohol or substance abuse. * Major infection within 4 weeks prior to the Baseline Visit. Exclusion Criteria: Caregiver for Participant with Dementia: • Diagnosis of mild cognitive impairment or dementia.
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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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University of Kentucky
Lexington, Kentucky, 40536, United States
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