Actively Recruiting
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
Eligibility Criteria
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
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
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
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
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
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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