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Clinical Trials/NCT02272933
NCT02272933WithdrawnNot Applicable

Operability and Implementation of a Patient Motion Monitoring System Using Wireless Body Worn Sensors

Texas Tech University Health Sciences Center2 sites in 1 countryStarted: August 2014Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Withdrawn
Locations
2
Primary Endpoint
Detection of Fall Incidences

Study Overview

Brief Summary

In this observational study, a motion monitoring system including body-worn sensors, communication portals, data capture system, and algorithms will be tested with geriatric patients in Garrison Geriatric Education and Care Center (Lubbock, TX). The study is part of a long-term effort to improve the quality of life and safety of geriatric patients by using autonomous systems that can alert care givers of mobility issues and falls.

Detailed Description

Medical monitoring systems have become an important area of research and development due to the possibility of allowing improved quality of life and care while reducing overall medical costs.

Significance of the study:

The study is significant because it will allow researchers to understand the efficacy of the autonomous sensor system used with actual residents of a geriatric care center. This study is one of the first attempts to monitor movements of geriatric residents as they go about their activities of daily living. This type of system has the potential to improve the quality of life and safety of geriatric patients.

Goals:

The development of autonomous patient monitoring technologies that will eventually improve the quality of life and safety of patients in geriatric care facilities and other environments.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
45 Years to 85 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • At least 30 day resident of Garrison.
  • Deemed mentally competent by primary care provider to make decisions regarding their daily shoe wear.
  • A resident prone to falls is eligible.
  • Willing to wear shoes and offer high level of compliance to study
  • Able to provide informed consent
  • Able to complete survey
  • Age range: 45-85 yrs

Exclusion Criteria

  • Unwilling to participate
  • Not mentally competent to provide informed consent

Outcomes

Primary Outcomes

Detection of Fall Incidences

Time Frame: 6 months

Participants will be monitored for falls. The detection of fall events as determined by the sensors will be compared to the fall log kept by Garrison Geriatric Center.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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