Patient Monitoring
Conditions
Keywords
mobile IoT technology, Patient Transfer Monitoring System
Brief summary
This trial is multi-center prospective study to develop Patient Transfer Monitoring system using mobile lot network and the Risk Factor Detection System and apply to real In-Hospital Patients and verify the efficacy.
Detailed description
Hospitalized patients who need transfer for a diagnostic examination or rehabilitation therapy during hospitalization, and have a risk of hypoxemia during transfer will be enrolled in this trial. The subjects will be provided with a portable oximeter and a smart-phone which application for monitoring is installed, and oxygen saturation and pulse rate will be checked in real time during transfer. The collected data will be transferred to cloud system via Iot network, and the transmitted data will be monitored in real time via monitoring equipment in the (Patient-hospitalized) ward. If there is a risk, the alarm system is activated so that the medical team is able to check risk factor and manage it immediately. All the risk factors and severity will be collected during transfer, also these are checked whether the monitoring system and the data transmission system work properly or not, the time from detecting risk factor to medical response, the composition of medical staffs who responding to alarmed risk factors and improvement of the subjects. Pilot study will be conducted with 20 subjects in Asan medical center. In pilot study, monitoring machines (HR, SpO2 monitor) commonly used in wards or hospitals will be used to verify the stability of oximeter used in this study and the developed risk detection system.
Interventions
OTHERPatient Transfer Monitoring System
The subjects will be provided with portable oximeter and smart-phone which application for monitoring is installed, and the transmitted data will be monitored in real time via monitoring equipment in the (Patient-hospitalized) ward.
Sponsors
Korea Health Industry Development Institute
Asan Medical Center
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
20 Years to 80 Years
Healthy volunteers
No
Inclusion criteria
* A hospitalized patients in pulmonology department or rehabilitation hospital who have a risk of decreasing oxygen saturation * A patients who require transfer in the hospital for a diagnostic examination or rehabilitation therapy during hospitalization * Patients who need oxygen saturation monitoring according to the investigator's judgment * Patients who voluntarily agree to study participation and provide written informed consent form
Exclusion criteria
* Patients who don't agree with the study procedure or are uncooperative * Repeated monitoring of the same patient who already registered in the tiral
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| frequency of risk factors which are detected during transfer | from the beginning to immediately after the end of the patient transfer | — |
| severity of risk factors which are detected during transfer | from the beginning to immediately after the end of the patient transfer | The severity is assessed as mild(risk factor was resolved without medical staff), moderate(resolved by medical staffs, but returned to the ward), and severe(not resolved by medical staffs, needs other method such as CPCR call, invasive intervention). |
| reason of decreased oxygen saturation | from the beginning to immediately after the end of the patient transfer | — |
| duration of decreased oxygen saturation | from the beginning to immediately after the end of the patient transfer | — |
| change from baseline in Oxygen saturation | from the beginning to immediately after the end of the patient transfer | — |
| the time from detecting risk factor to medical response | from the beginning to immediately after the end of the patient transfer | — |
| Death | from admission to discharge, up to 8 months | — |
| admission to intensive care units | from admission to discharge, up to 8 months | — |
| Adverse events related to the study | from the beginning to immediately after the end of the patient transfer | — |
| medical staffs who managed the alarmed event during transfer | from the beginning to immediately after the end of the patient transfer | — |
Countries
South Korea
Outcome results
None listed