Usability Validation of Patient Monitoring Device for Pressure Injury Prevention and Fall Detection

Masimo Corporation34 enrolled

Overview

This study describes a procedure to collect a subject's position, movement, physiological data and usability information using Masimo's investigational device.

Study Type

INTERVENTIONAL

Allocation

Purpose

OTHER

Masking

NONE

Enrollment

Conditions

Pressure Ulcer Pressure Injury Falls Injury

Interventions

Masimo Centroid SystemDEVICE

Noninvasive positional monitoring device

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: 1. At least 18 years of age 2. ICU patient 3. Primarily bedbound subjects 4. Able to be monitored for a minimum of approximately 8 hours Exclusion Criteria: 1. Pregnancy 2. Prisoner status 3. Pressure injury stage 2, 3, or ungroupable 4. Has a pacemaker or internal defibrillator 5. Has a history of complications with a similar study 6. Has any medical condition which in the judgment of the Investigator, renders them inappropriate for participation in this study

Locations (1)

Baylor University Medical Center

Dallas, Texas, United States

Outcomes

Primary Outcomes

Usability Validation of Masimo Centroid System

The number of participants enrolled to assess the usability of the Masimo Centroid System.

Time frame: At least 8 hours

Data from ClinicalTrials.gov

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