Feasibility of Passive Data Collection in Dementia Subjects With Agitation

Completed

• Conditions: Alzheimer Disease; Dementia; Frontotemporal Dementia; Lewy Body Dementia; Mixed Dementia; Vascular Dementia

• Registration Number: NCT04413851
• Lead Sponsor: HealthMode Inc.

Brief Summary

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.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2020-05-29
• Study First Submitted QC: 2020-05-29
• Study Start: 2020-06-01
• Study First Posted: 2020-06-04
• Status Verified: 2021-12
• Primary Completion: 2021-12-06
• Study Completion: 2021-12-06
• Last Update Submitted: 2021-12-16
• Last Update Posted: 2021-12-17

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 1

Inclusion Criteria

• Male and female subjects 18 years and older.
• Subjects who have met DSM-5 criteria for Dementia (all cause)
• Subjects with a recent history of agitation in the past 6 months to a point that impairs social activities, requires staffing or medical intervention (kick, bite, flailing, etc.), impairs ability for functional activities of daily living, as disclosed by a caregiver or documented in the medical record.
• Subjects resident in a group home, nursing home, or assisted living are eligible to participate.
• Subjects who can read, understand and provide written informed consent or who have a Legally Acceptable Representative (LAR)
• Subjects who are willing and able to carry a smartphone and wear an activity tracker on their wrist or hand, alone or with the help of a caregiver.
• Subjects who, either alone or with a caregiver, are able to operate a smartphone and wrist or hand-worn activity tracker, alone or with the help of a caregiver.
• Subjects who are in good general health prior to study participation as determined by a detailed medical history, and in the opinion of the Principal Investigator.
• Subjects, who are able to ambulate without an assistive device, or with a single point cane.

Exclusion Criteria

• Subjects who are unwilling or unable to carry a smartphone and wear an activity tracker on their wrist or hand.
• Subjects with serious or unstable medical illnesses. These include current hepatic (moderate-severe hepatic impairment), renal, gastroenterological, respiratory, cardiovascular (including ischemic heart disease, congestive heart failure), endocrinologic, neurologic or hematologic disease.
• Subjects who are considered by the investigator, for any reason, to be an unsuitable candidate.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Feasibility of passive and continuous data collection	28 days	Total time and percentage of continuous data collection for each stream of data aiming for \>50% coverage.

Secondary Outcome Measures

Name	Time	Method
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.	28 days	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.

Trial Locations

Locations (2)

Tucson Neuroscience Research, LLC; 🇺🇸 Tucson, Arizona, United States

Virtual Research Site; 🇺🇸 New York, New York, United States