MedPath

Artificial Intelligence + Care Coach Intervention

Not Applicable
Completed
Conditions
Caregiver
Artificial Intelligence
Care Transition
Dementia
Emergency Department
Registration Number
NCT05352399
Lead Sponsor
Yale University
Brief 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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
40
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Intervention Appropriateness MeasureDay 7 and 30

Appropriateness is defined as the perceived fit, relevance, or compatibility of the innovation for a given setting or consumer, and/or perceived fit of the innovation to address a particular issue or problem. The measure consists of 4 questions, with an overall score range of 4-20 (higher scores suggest increased appropriateness). Administration time is 1-2 minutes. Measured by survey.

Feasibility of Intervention MeasureDay 7 and 30

Feasibility is defined as the extent to which a new innovation can be successfully used or carried out within a given setting. The measure consists of 4 questions, with an overall score range of 4-20 (higher scores suggest increased feasibility). Administration time is 1-2 minutes. Measured by survey.

Acceptability of Intervention MeasureDay 7 and 30

Acceptability is defined as the perception that a given innovation is agreeable, palatable, or satisfactory. The measure consists of 4 questions, with an overall score range of 4-20 (higher scores suggest increased acceptability). Administration time is 1-2 minutes. Measured by survey.

System Usability ScaleDay 7 and 30

Usability encapsulates several aspects including subjective component assessments of effectiveness, efficiency, and satisfaction. The System Usability Scale consists of 10 questions on effectiveness, efficiency, and satisfaction, with an overall score range of 10-50 (higher scores suggest increased usability). Administration time is 3-5 minutes. Measured by survey.

Secondary Outcome Measures
NameTimeMethod
Quality of Life (QOL) in Alzheimer's Disease (AD) Scale (QOL-AD)Day 0, 7 and 30

Total score range 13-52; higher scores indicate better QOL.

Dyadic Relationship Scale (DRS)Day 0, 7 and 30

DRS to measure strain between the caregiver and recipient within the last 30 days. Total score range 4-20. High scores indicate high levels of strain.

Zarit Caregiver Burden ScaleDay 0, 7 and 30

The Zarit Caregiver Burden Scale consists of 4 items with the total score ranging between 0-16. Higher scores indicate greater burden. Administration time is approximately 10-15 minutes. Measured by survey.

Fortinsky Caregiver Self-Efficacy ScaleDay 0, 7, and 30

Used to evaluate the coping ability of daily living. The measure has a total score range from 10-100, with higher scores representing greater self-efficacy. Administration time is approximately 3-5 minutes. Measured by survey.

Trial Locations

Locations (1)

Yale New Haven Hospital

🇺🇸

New Haven, Connecticut, United States

Yale New Haven Hospital
🇺🇸New Haven, Connecticut, United States

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