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Feasibility of Passive Data Collection in Dementia Subjects With Agitation

NCT04413851 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1

Last updated 2021-12-17

No results posted yet for this study

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

  • Dementia
  • Alzheimer Disease
  • Vascular Dementia
  • Frontotemporal Dementia
  • Lewy Body Dementia
  • Mixed Dementia

Sponsors & Collaborators

  • HealthMode Inc.

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-06-01
Primary Completion
2021-12-06
Completion
2021-12-06

Countries

  • United States

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04413851 on ClinicalTrials.gov