Actively Recruiting

Phase Not Applicable
Age: 0 - 24Months
All Genders
ID06932341

The Impact of EHR-Alerts on the Use of an EHR-Integrated Clinical Decision Support Pathway and the Use of High Flow Nasal Cannula in Bronchiolitis

Led by Johns Hopkins University · Updated on 2026-05-29

8000

Participants Needed

3

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying how different types of alerts in Electronic Health Records (EHR) affect doctors' use of clinical guidelines for treating bronchiolitis in young children. Bronchiolitis is a common viral illness affecting infants and toddlers under 2 years old, often leading to hospitalization. The study aims to find out if these alerts increase use of evidence-based care and reduce unnecessary treatments like low-value High Flow Nasal Cannula (HFNC) use, which can lead to longer hospital stays and higher costs. The study randomly assigns children under 2 years old who come to the hospital with bronchiolitis indicators into three groups. One group’s doctors receive no EHR alert, the second group’s doctors receive an interruptive alert requiring interaction, and the third group’s doctors see a non-interruptive visual alert. All groups continue to have access to the evidence-based clinical guideline embedded in the EHR. Researchers will compare guideline use between these groups and assess how guideline use affects HFNC use and other care elements. Participants will receive usual hospital care during the study. Researchers will measure how often doctors use the EHR clinical decision support tool from the time of enrollment until the end of the emergency visit or hospital stay (up to 4 days). They will also look at orders placed through the tool and impacts on care outcomes like ICU admission, length of hospital stay, and readmissions. This study is led by Johns Hopkins University and aims to improve care quality for children with bronchiolitis.

CONDITIONS

Brief Title

Evaluation of the Impact of EHR-Alerts on Clinical Decision Support Pathway Use in Bronchiolitis, and the Impact of Pathway Use on the Prescription of High Flow Nasal Cannula and Other Elements of High Value Care.

Who Can Participate

Age: 0 - 24Months
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Children 24 months of age or younger presenting to the emergency room and/or hospitalized with electronic health record indicators of bronchiolitis at one of three study sites
  • Indicators include use of bronchiolitis-specific order sets or combinations of emergency department complaints, infection or isolation status, and receipt of relevant therapies such as oxygen supplementation
Not Eligible

You will not qualify if you...

  • Current encounter is a birth encounter
  • Child is currently hospitalized in an intensive care unit (ICU)
  • Hospital stay longer than 14 days

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person) at emergency room or hospital admission

Treatment

Duration - Up to 4 days or until hospital discharge

Participants are randomized to receive either no EHR-alert, an interruptive EHR-alert, or a non-interruptive EHR-alert to guide clinical decision support for bronchiolitis during their emergency department visit or hospital stay.

1 baseline visit during emergency department or hospital stay

Trial Site Locations

Total: 3 locations

1

Johns Hopkins All Children's Hospital

St. Petersburg, Florida, United States, 33701

Actively Recruiting

2

Johns Hopkins Bayview Medical Center

Baltimore, Maryland, United States, 21224

Actively Recruiting

3

Johns Hopkins Children's Center

Baltimore, Maryland, United States, 21287

Actively Recruiting

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Research Team

B

Benjamin E Bodnar, MD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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