Skip to content

Non-Interruptive Alerts for Improving Use of Clinical Decision Rules

The Use of Non-Interruptive Alerts for Improving the Use of Clinical Decision Rules in the Emergency Department: A Cluster Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04702308
Enrollment
70
Registered
2021-01-08
Start date
2021-02-18
Completion date
2022-11-04
Last updated
2023-11-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chest Pain, Deep Vein Thrombosis, Minor Head Injury, Neck Trauma, Pulmonary Embolism

Keywords

clinical decision support, clinical decision rules

Brief summary

This study is an extension of a planned quality improvement project that aims to promote standard of care by increasing the use of evidence-based clinical decision rules amongst emergency medicine providers in the University of Utah Emergency Department. Patient-specific information from the EHR will be used to recommend the use of relevant clinical decision rules to emergency medicine providers at the point-of-care. These recommendations will be in the form of non-interruptive alerts with one-click access to the suggested decision rules through the MDCalc Connect EHR add-on application. Specific aims of the study are to determine if 1) patient-specific non-interruptive alerts increase the use of clinical decision rules amongst emergency medicine providers and 2) an increase in the use of clinical decision rules affects provider ordering habits.

Interventions

OTHERClinical Decision Rule Alerts

The

Sponsors

University of Utah
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Intervention model description

Cluster randomized controlled trial

Eligibility

Sex/Gender
ALL
Age
16 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Patient Inclusion Criteria: * 16 years of age or older * Qualifying chief complaint\* Patient

Exclusion criteria

* None * A full list of the qualifying chief complaints is provided in Appendix A of the full research protocol.

Design outcomes

Primary

MeasureTime frameDescription
Total clinical decision rule usageDuring the interventionComposite measure of total number of clinical decision rules used through the MDCalc Connect app.

Secondary

MeasureTime frameDescription
Computed tomography pulmonary angiography studiesDuring the interventionThe total number of computed tomography pulmonary angiography studies ordered
Computed tomography head studiesDuring the interventionThe total number of computed tomography head without contrast studies ordered
Computed tomography c-spine studiesDuring the interventionThe total number of computed tomography c-spine without contrast studies ordered
Lower extremity ultrasoundDuring the interventionThe total number of lower extremity ultrasound studies ordered
Individual clinical decision rule usageDuring the interventionNumber of uses of individual clinical decision rules measured through the MDCalc Connect app.
Delta troponin testsDuring the interventionTotal number of times two or more troponin tests were ordered
Emergency department bounceback rate.Up to 30 days after the intervention30-day emergency department return visit (or bounceback) rate
Admission rateDuring the interventionHospital admission rate
d-dimer testsDuring the interventionTotal number of d-dimer blood tests ordered

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026