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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06140342
Other study ID # 3-P30-AG-073105-02 SUPPLEMENT
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date August 1, 2023
Est. completion date January 1, 2025

Study information

Verified date November 2023
Source Autotune Me LLC
Contact Kendra Ray, PhD, MBA, MPH
Phone 347-636-7157
Email kendra@autotuneme.org
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this pilot is to develop a mobile application that detects physiological measures of individuals with Alzheimer's disease and related dementias and triggers auto-play of personalized songs in a wearable device. The investigators will test the feasibility and acceptability of the app. This app may be an important tool to include in daily caregiving in a home setting by extending established benefits of music therapy for people with Alzheimer's disease and related dementias.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date January 1, 2025
Est. primary completion date January 1, 2025
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria for person with dementia - A person with ADRD exhibits neuropsychiatric symptoms of dementia such as agitation, restlessness, depressed mood, etc. - Stability with or without psychotropic or anti-depressant medications - Ability to hear with or without an assistive device Inclusion Criteria for Caregivers - Family or close friend caregiver of persons with dementia - Must be able to read and write in basic English Exclusion Criteria for all participants - Inadequate hearing - History of psychosis or other mental disorders other than depression - Presence of substance or alcohol abuse

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Feasibility study of music-based mobile app
To determine the performance and usability of the app, 20 dyads will be recruited to test it for 2 weeks. The investigators will collect physiological measures based on the application's demonstration to auto-play music according to movement or sedentary states.

Locations

Country Name City State
United States Autotune Me, LLC Brooklyn New York

Sponsors (3)

Lead Sponsor Collaborator
Autotune Me LLC National Institute on Aging (NIA), University of Pennsylvania

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Usability of mobile app Dyads of caregivers of people with dementia and their caregivers will wear a smartwatch and test the music-based mobile app for two weeks. The person with dementia will wear the smartwatch that will connect to the mobile app for 2 weeks. Caregivers will be asked to complete a daily checklist of their care recipients' behaviors for two weeks.
Participants will complete the Usefulness, Satisfaction and Ease of Use questionnaire that describes the usability of the mobile app. The minimum score is 30 while the maximum score is 240. The higher the score means the usability of the app is more acceptable.
2 weeks
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