This is a multi-center, observational, feasibility study, to evaluate long term passive data collection, data quality, and user experience of HealthMode Agitation (Apps) to collect motion, location, physiological, and audio data; and eCOA and EMA responses with mobile devices (iPhone, Apple Watch). The purpose of this study is to evaluate and improve HealthMode Apps data collection and usability in subjects experiencing agitation in the context of dementia.
Study Type
OBSERVATIONAL
Enrollment
1
Tucson Neuroscience Research, LLC
Tucson, Arizona, United States
Virtual Research Site
New York, New York, United States
Feasibility of passive and continuous data collection
Total time and percentage of continuous data collection for each stream of data aiming for \>50% coverage.
Time frame: 28 days
Tolerability of carrying a smartphone and wearing a data collection sensor on the wrist and/or hand in a population of subjects who may have frequent episodes of agitation or impulsive behavior.
Caregiver and Staff engagement with the eCOA and EMA (threshold 80% completion) and responses to usability questionnaires at week 1 and 4 to provide feedback on comfort, usability and engagement. The score ranges from 10 to 50, higher score indicating a better usability.
Time frame: 28 days
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