Viewing Study NCT05557331



Ignite Creation Date: 2024-05-06 @ 6:07 PM
Last Modification Date: 2024-10-26 @ 2:42 PM
Study NCT ID: NCT05557331
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-07-01
First Post: 2022-09-18

Brief Title: Effectiveness of a Mobile App in Reducing Therapeutic TAT in an Emergency Department
Sponsor: Pediatric Clinical Research Platform
Organization: Pediatric Clinical Research Platform

Study Overview

Official Title: Effectiveness of a Mobile App PIMPmyHospital in Reducing Therapeutic Turnaround Times in an Emergency Department Protocol for a Pre-Post Intervention Study
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-06
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This study is a single center non-equivalent comparison group pre-post study in a tertiary pediatric emergency department in Switzerland the study will compare the control and experimental groups on outcome measures before 12-month period and after 6-month period the intervention consisting of the implementation and use of the evidence-based mobile app-the Patients In My Pocket in my Hospital PIMPmyHospital app

The primary outcome will be the mean elapsed time in minutes between the delivery of lab results and the emergency department caregivers accessing them before ie on the institutional electronic medical records and after the implementation of the app ie directly on the app
Detailed Description: The study objective is to evaluate whether the use of the PIMPmyHospital app alters emergency departments ED physicians and nurses temporal efficiency to learn about laboratory results more quickly while actively working in an ED Temporal efficiency will be assessed by measuring the time between the release of the laboratory results in the clinical information system and their acknowledgement by these clinicians Information regarding the app has been published previously doiorg103390jpm12030428

The investigators will conduct an 18-month single center non-equivalent comparison group pre-post study The study will compare the control and experimental groups on outcome measures before 12-month period and after 6-month period the intervention consisting of the use of the app The study will take place in the pediatric ED of a tertiary referral and major trauma hospital in Switzerland with an annual volume of 35000 visits

Eligible participants will be postgraduate residents pursuing a 6-year residency in pediatrics pediatric emergency medicine fellows and registered nurses from the pediatric ED aged 18 years Written informed consent will be obtained from each participant in the interventional group after full information disclosure prior to study participation

Before the implementation of the app electronic medical records EMR-based data from the past 12 months will be collected retrospectively These data include the times ie HHMMSS that results issued by the central laboratory were available on the institutionals EMR as well as the times at which these results were accessed by caregivers via conventional computerized workstations ii After the implementation of the app data will be collected prospectively over a 6-month period of use This will include the times HHMMSS when the results issued by the central laboratory are made available on caregivers mobile app and access times as well as concurrent or preferred access times on the conventional computerized workstations should this occur Individual acceptance of the app on the first day a priori and then on the last day of the intervention will be evaluated through the Unified Theory of Acceptance and Use of Technology UTAUT Usability of the app will be measured by the System Usability Scale SUS

The primary outcome will be the mean elapsed time in minutes between the delivery of the lab results and the caregiver accessing them both before and after the implementation of the app

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None