NCT04702308

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
70

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Feb 2021

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 4, 2021

Completed
4 days until next milestone

First Posted

Study publicly available on registry

January 8, 2021

Completed
1 month until next milestone

Study Start

First participant enrolled

February 18, 2021

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 18, 2021

Completed
12 months until next milestone

Study Completion

Last participant's last visit for all outcomes

November 4, 2022

Completed
Last Updated

November 18, 2023

Status Verified

November 1, 2023

Enrollment Period

9 months

First QC Date

January 4, 2021

Last Update Submit

November 16, 2023

Conditions

Keywords

clinical decision supportclinical decision rules

Outcome Measures

Primary Outcomes (1)

  • Total clinical decision rule usage

    Composite measure of total number of clinical decision rules used through the MDCalc Connect app.

    During the intervention

Secondary Outcomes (9)

  • Individual clinical decision rule usage

    During the intervention

  • Computed tomography pulmonary angiography studies

    During the intervention

  • Computed tomography head studies

    During the intervention

  • Computed tomography c-spine studies

    During the intervention

  • Lower extremity ultrasound

    During the intervention

  • +4 more secondary outcomes

Study Arms (2)

Intervention Group

EXPERIMENTAL

The intervention will contain two components: 1) a non-interruptive best practice advisory (BPA) in the Epic Storyboard and 2) a default suggested calculator tab in the MDCalc Connect app. Six clinical decision rules will be included: Canadian CT Head Rule, Canadian C-spine Rule, HEART Score, PERC Rule, Wells' PE Criteria and Wells' DVT Criteria. Predefined criteria based on chief complaint, patient age and vital signs will be used to determine when a decision rule may be relevant in a patient encounter. When a patient meets all of the predefined criteria, the intervention will be triggered.

Other: Clinical Decision Rule Alerts

Control Group

NO INTERVENTION

The control group will be usual care. Specifically, providers in the control group will not receive the clinical decision rule alert or the default suggested calculator tab in the MDCalc Connect app. The control group providers will have access to the MDCalc Connect app in its standard form and functionality.

Interventions

The

Intervention Group

Eligibility Criteria

Age16 Years+
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • years of age or older
  • Qualifying chief complaint\*

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Utah

Salt Lake City, Utah, 84112, United States

Location

MeSH Terms

Conditions

Pulmonary EmbolismVenous ThrombosisCraniocerebral TraumaChest Pain

Condition Hierarchy (Ancestors)

Lung DiseasesRespiratory Tract DiseasesEmbolismEmbolism and ThrombosisVascular DiseasesCardiovascular DiseasesThrombosisTrauma, Nervous SystemNervous System DiseasesWounds and InjuriesPainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
DIAGNOSTIC
Intervention Model
PARALLEL
Model Details: Cluster randomized controlled trial
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Postdoctoral Fellow

Study Record Dates

First Submitted

January 4, 2021

First Posted

January 8, 2021

Study Start

February 18, 2021

Primary Completion

November 18, 2021

Study Completion

November 4, 2022

Last Updated

November 18, 2023

Record last verified: 2023-11

Locations