Feasibility of a Wireless Monitoring System as an Alternative to Current Bedside MonitorsInvestigators: - Trial PACTR202212474343995
Access comprehensive clinical trial information for PACTR202212474343995 through Pure Global AI's free database. This Not Applicable trial is sponsored by Dr Fizan Abdullah Northwestern University; North Western University and is currently Not yet recruiting. The study focuses on Surgery.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to Pan Africa Clinical Trials Registry data, helping medical device and pharmaceutical companies navigate clinical research efficiently.
Study Focus
device
Sponsor & Location
Dr Fizan Abdullah Northwestern University; North Western University
Fizan Abdullah; Ann and Robert H Lurie Chidrens Hospital and North Western University
Timeline & Enrollment
Not Applicable
Jan 01, 1900
Jan 01, 1900
Summary
Background: Current post-operative monitoring practices of patients at Korle-Bu teaching hospital rely on manual blood pressure, temperature and heart rate monitoring which are inefficient, and often miss the onset of complications. Consumer-grade wearables (e.g., Fitbit and Xiaomi band), which collect vital signs similar to clinical-grade monitors and transmit them in near-real time to a smartphone/IPad and then to a cloud-based platform that allows further processing of data, provide an opportunity to implement a wireless monitoring system as an alternative to current bedside monitors. ii. General Aim: To establish the feasibility of a Fitbit/Xiaomi band-based wireless monitoring system for post-operative in-hospital monitoringiii. Methodology: Fifteen (15) inpatient (pediatric appendicitis), and 15 accident centre patients (adult and pediatric trauma) will be recruited at the Korle Bu Teaching Hospital at two sites: the inpatient pediatric surgery wards, and the accident centre. A Fitbit/Xiaomi band will be placed on each inpatientโs wrist on postoperative day 1 and until they are discharged, and on each trauma patientโs wrist while in the accident centre. The Fitbit/Xiaomi band will be linked using Bluetooth technology to an IPad or iPhone, and data will be streamed to the IDataPoint cloud-based platform that will be accessible to the nurse on the IPad or iPhone, and on the surgeonโs phone. Fitbit and Xiaomi band data will be downloaded and compared to manually obtained vitals from the patient medical charts. At the conclusion of the study, all study participants, parents and up to 10 healthcare workers will be invited to participate in a voluntary semi-structured interview to ascertain perspectives from the respective individuals.iv. Expected Outcome At the end of this study, we hope to establish the feasibility of this wireless monitoring system as a means of monitoring patients postoperatively and after trauma and pave the way for further evaluation
ICD-10 Classifications
Data Source
Pan Africa Clinical Trials Registry
PACTR202212474343995
Device Trial

