Skip to main content
Clinical Trials/NCT02659982
NCT02659982
Completed
Not Applicable

Study Protocol for Evaluation of EarlySense Home Care Tele-monitoring Device - A Contact-Free System for Measuring Heart Rate, Respiratory Rate and Motion For Early Detection of Deterioration For Cardiac Patients at Home

EarlySense Ltd.1 site in 1 country50 target enrollmentApril 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Post Cardiac Surgery
Sponsor
EarlySense Ltd.
Enrollment
50
Locations
1
Primary Endpoint
To evaluate if Alerts and Flags generated by the EarlySense Home Care System, could have potentially prevented readmission to hospitals, and providing better care at home, for post cardiac surgery patients
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The aim of this study is to evaluate the relevance of the information as provided by the EarlySense Home care Tele-monitoring system can provide relevant flagging information for clinicians to identify the patients at higher risk to proactively assess patients' condition

Detailed Description

Study objectives include: 1. Assess if and to what extent the flags provided by EarlySense Home care tele-monitoring provides relevant clinical information that can help case managers / nurses of home care agency to detect patients who need further assessment and perhaps early intervention to minimize hospitalization (re-admission to hospital). 2. Use data to further optimize a decision algorithm utilizing changes in physiological data over time (i.e., hours to days) which may identify patients at higher risk for poor outcomes (flagging algorithm). 3. Assess the acceptability of the EarlySense Home care device by clinicians 4. Assess the acceptability of the EarlySense Home care device by patients at home and their families, in their own home as determined by a provided questioner

Registry
clinicaltrials.gov
Start Date
April 2015
End Date
April 2017
Last Updated
8 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age 21 and up
  • Any patient hosted in Shelev with geographically resident over 50 km from Sheba Medical Center/ Shelev
  • Patients agrees to sign the consent form and comply with study protocol.

Exclusion Criteria

  • Patients do not agree to sign the consent form
  • Planned readmission within 30 days of discharge from hospital
  • Going home to hospice care.
  • Patients with cognitive constraints or disabilities

Outcomes

Primary Outcomes

To evaluate if Alerts and Flags generated by the EarlySense Home Care System, could have potentially prevented readmission to hospitals, and providing better care at home, for post cardiac surgery patients

Time Frame: 30 days

Evaluate the usability of Home Monitoring System activity indication such as number of hours spent in bed during the day in providing help to nurses, evaluating the overall clinical situation of post cardiac petients at home

Study Sites (1)

Loading locations...

Similar Trials