Clinical Trials Directory

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CompletedNCT04413851

Feasibility of Passive Data Collection in Dementia Subjects With Agitation

A Feasibility Study to Evaluate Passive Collection of Activity Data in Subjects With Agitation in the Context of Dementia

Status
Completed
Phase
Study type
Observational
Enrollment
1 (actual)
Sponsor
HealthMode Inc. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Conditions

Timeline

Start date
2020-06-01
Primary completion
2021-12-06
Completion
2021-12-06
First posted
2020-06-04
Last updated
2021-12-17

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT04413851. Inclusion in this directory is not an endorsement.

Feasibility of Passive Data Collection in Dementia Subjects With Agitation (NCT04413851) · Clinical Trials Directory