MedPath

Testing of Medication Dosing Software

Not Applicable
Not yet recruiting
Conditions
Pediatric Emergency Medicine
Interventions
Device: Standard practice
Device: Medication dosing software
Registration Number
NCT06129370
Lead Sponsor
Nura Medical
Brief Summary

The goal of this clinical study is to evaluate the clinical efficiency of a medication dosing software in simulated pediatric emergency care. The main questions it aims to answer are:

* Will the time to patient be significantly reduced with the medication dosage software when compared to standard clinical practice?

* Will the time to calculate dosage of medications be significantly reduced with the medication dosage software when compared to standard clinical practice?

* How will users perceive clinical efficiency, ease of use, confidence level of using the medication dosage software when compared to standard clinical practice?

* How will accuracy of medication dose and volume calculations as well as final volume ready for administration using the medication dosage software compared to standard clinical practice?

* Will the time spent calculating medication doses by the second healthcare professional on pediatric non-acute and acute care cases be significantly reduced with the medication dosage software when compared to standard clinical practice?

Participants will be presented pediatric care scenarios and asked to calculate and prepare intravenous medications under two interventions: the medication dosage software and standard clinical practice (Lexicomp and manual calculator).

Detailed Description

Not available

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
12
Inclusion Criteria

-Healthcare professionals who have worked or who are currently working at a healthcare facility and involved in the calculation or preparation of IV medication.

Exclusion Criteria
  • Healthcare professionals who cannot read, speak, or understand English or French as the simulations will be conducted in English or French.
  • Performance of physically strenuous activity 30 min prior to study.
  • Physical limitations that affect performance on required tasks (e.g., inability to place arm cuff on mannequin's arm, inability to handle weight estimation and touchscreen devices).

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Software, then StandardStandard practiceParticipants will use the medication dosage software to calculate and prepare intravenous medications during the initial run through of pediatric case scenarios. Then, they will use standard clinical practice (Lexicomp and manual calculator) during the second run through of pediatric case scenarios.
Standard, then SoftwareStandard practiceParticipants will use standard clinical practice (Lexicomp and manual calculator) to calculate and prepare intravenous medications during the initial run through of pediatric case scenarios. Then, they will use the medication dosage software during the second run through of pediatric case scenarios.
Standard, then SoftwareMedication dosing softwareParticipants will use standard clinical practice (Lexicomp and manual calculator) to calculate and prepare intravenous medications during the initial run through of pediatric case scenarios. Then, they will use the medication dosage software during the second run through of pediatric case scenarios.
Software, then StandardMedication dosing softwareParticipants will use the medication dosage software to calculate and prepare intravenous medications during the initial run through of pediatric case scenarios. Then, they will use standard clinical practice (Lexicomp and manual calculator) during the second run through of pediatric case scenarios.
Primary Outcome Measures
NameTimeMethod
Time to calculateThrough study completion, up to 3 months

Assess the time to calculate medication dosage using the medication dosage software compared to standard clinical practice

TIme to patientThrough study completion, up to 3 months

Assess the time elapsed from ordering of medication to ready for administration using the medication dosage software compared to the time achieved with standard clinical practice

Secondary Outcome Measures
NameTimeMethod
AccuracyThrough study completion, up to 3 months

To assess the accuracy of (I) medication dose and volume calculations and (II) final volume ready for administration using the medication dosage software compared to standard clinical practice.

FeedbackThrough study completion, up to 3 months

time to calculate medication dosage using the medication dosage software compared to standard clinical practice

Time of calculation by second healthcare professionalThrough study completion, up to 3 months

To assess the time spent calculating medication dosages by the second healthcare professional.

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