Actively Recruiting
Multi-modal Large Language Model-Empowered Talk Therapy for Older Adults With ADRD
Led by Indiana University · Updated on 2026-05-06
60
Participants Needed
1
Research Sites
77 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of this study is to test the usefulness and the effect of Smart Virtual Reminiscence (SVR) therapy intervention on the Behavioral and Psychological Symptoms of Dementia (BPSD) of patients with Alzheimer's Disease and Related Dementias (ADRD). SVR is designed to help older adults improve their psychological well-being and cognition. This research supports our long-term goal of designing and implementing intelligent interactive systems to improve the health of individuals with ADRD.
CONDITIONS
Official Title
Multi-modal Large Language Model-Empowered Talk Therapy for Older Adults With ADRD
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Participants aged 65 years or older
- Diagnosed with mild cognitive impairment (MCI) or mild Alzheimer's Disease and Related Dementias (ADRD)
- Access to a reliable internet connection
- Living in the community (not in assisted living or nursing home)
- Elevated behavioral and psychological symptoms of dementia (BPSD) with a Healthy Aging Brain Care monitor score above 14
- Presence of one or more BPSD behaviors such as agitation, anxiety, depression, apathy, or sleep disturbances
- Ability to consent for themselves
- Care partners aged 21 years or older who are knowledgeable about the patient's behaviors and will participate in the study
You will not qualify if you...
- Living in an assisted living facility or nursing home
- Moderate to severe ADRD as measured by the Quick Dementia Rating System
- Life expectancy less than 6 months
- Care partner with mild cognitive impairment or dementia
- Care partner with severe mental illness or substance abuse
- Care partner with life expectancy less than 6 months
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Sidney & Lois Eskenazi Hospital
Indianapolis, Indiana, United States, 46202
Actively Recruiting
Research Team
K
Katrina Coppedge, BA
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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