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Supporting Care Partners' Well-Being With Artificial Intelligence (AI) Chatbots

Supporting Care Partners' Well-Being With AI Chatbots: A Feasibility and Acceptability Study

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07145723
Enrollment
26
Registered
2025-08-28
Start date
2025-09-22
Completion date
2026-02-04
Last updated
2026-04-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Caregivers

Keywords

Caregivers for adults with dementia, Surveys, Care partners, Artificial intelligence (AI) mobile application, Quality of life, Chatbot

Brief summary

This study is being completed to test an AI therapy chatbot application called Earkick to see whether it is feasible and acceptable in supporting care partners who support individuals living with dementia.

Interventions

OTHEREarkick app

Participants will have a baseline visit followed by an 8-week home monitoring period (HMP) using the Earkick app. The Earkick app will interact with a mental health chatbot. Participants will complete online surveys at the midpoint (4 weeks) and end (8 weeks) of the HMP. Participants will choose one mental health-related topic to focus on from weeks 1-4 and one physical health-related topic to focus on from weeks 5-8. Additionally, participants will have a post-HMP interview over Zoom.

Sponsors

University of Michigan
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Participants need to be a care partner (informal caregiver) of an individual living with dementia * Participant provides emotional, physical, and/or financial support/assistance to the individual with dementia (per protocol) * Participants indicate high levels of caregiver burden, confirmed using the 12-item Zarit Burden questionnaire (per protocol) * Provide informed consent and read, speak, and understand English * Have an Apple smartphone, tablet, or laptop, have access to the internet and text messages, and be willing to use this device as well as internet and text message access for the study, including downloading the AI chatbot app * Be willing to complete all study assessments

Exclusion criteria

* Professional, paid caregivers * Anything that would preclude safe or meaningful participation in the study

Design outcomes

Primary

MeasureTime frameDescription
Feasibility and Acceptability as measured by the Feasibility and Acceptability Questionnaire4 weeks and 8 weeks (post intervention)Feasibility and Acceptability Questionnaire (items are scaled from 1 to 5 to indicate level of agreement, where "1" indicates "strong disagreement" and "5" indicates "strong agreement").

Secondary

MeasureTime frame
Attrition as measured by the percent of participants completing the study8 weeks
Adherence as measured by the percentage of missing data over the course of the study8 weeks

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORMark Newman, PhD

University of Michigan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 2, 2026