N/A
Completed N=40
Artificial Intelligence + Care Coach Intervention
Dementia · Caregiver · Emergency Department · Artificial Intelligence
Source: ClinicalTrials.gov NCT05352399 ↗
Enrolled (actual)
40
Serious AEs
0.0%
Results posted
Aug 2025
Primary outcomePrimary: Intervention Appropriateness Measure — 15.1; 15.8 score on a scale
Summary
The purpose of this research study is to develop and test an artificial intelligence intervention for emergency department (ED) discharge care transitions experienced by caregivers of older adults with cognitive impairment.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Intervention Appropriateness Measure |
15.1; 15.8 | — |
| PRIMARY Feasibility of Intervention Measure |
15.1; 15.5 | — |
| PRIMARY Acceptability of Intervention Measure |
15.9; 15.8 | — |
| PRIMARY System Usability Scale |
30.1; 29.7 | — |
| SECONDARY Quality of Life (QOL) in Alzheimer's Disease (AD) Scale (QOL-AD) |
40.5; 33.8; 36.6 | — |
| SECONDARY Dyadic Relationship Scale (DRS) |
10.7; 10.4; 10.8 | — |
| SECONDARY Zarit Caregiver Burden Scale |
9.2; 9; 8.2 | — |
| SECONDARY Fortinsky Caregiver Self-Efficacy Scale |
52; 57.6; 65.8 | — |
Eligibility Criteria
Inclusion Criteria
- age ≥65 years with a diagnosis of dementia within the electronic health record OR new cognitive impairment identified during an ED visit
- be fluent in English or Spanish
- discharge after an ED visit
- possession of a smart device (either a phone, tablet, or computer) that has internet access to utilize and interact with NeuViCare AI services
Exclusion Criteria
- evidence of delirium, by the 4-AT screening tool
Data sourced from ClinicalTrials.gov (NCT05352399). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.