Actively Recruiting

Phase Not Applicable
Age: 0 - 24Months
All Genders
NCT06932341

Leveraging Electronic Health Record Tools to Improve the Evidence-Based Treatment of Children Hospitalized With Bronchiolitis

Led by Johns Hopkins University · Updated on 2025-05-08

800

Participants Needed

3

Research Sites

60 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this experimental study is to learn whether different types of best practice advisories (BPAs) that direct clinicians to reference clinical guidelines embedded in the electronic health record (EHR) increase the delivery of evidence-based care in children presenting to the hospital with bronchiolitis. The main questions it aims to answer are: * Do BPAs improve clinicians' delivery of guideline-concordant care in bronchiolitis? * Do interruptive BPAs improve guideline-concordant care of bronchiolitis more than non-interruptive BPAs? Researchers will compare the treatment and outcomes of patients whose clinicians did not receive a BPA, to those whose clinicians received a non-interruptive BPA, to those whose clinicians received an interruptive BPA. Patients will continue to receive standard hospital care for bronchiolitis. Clinicians will: * retain access to an EHR-embedded clinical guideline for bronchiolitis care * be exposed to either no BPA, a non-interruptive BPA, or an interruptive BPA promoting the EHR-embedded clinical guideline (randomized per patient encounter)

CONDITIONS

Official Title

Leveraging Electronic Health Record Tools to Improve the Evidence-Based Treatment of Children Hospitalized With Bronchiolitis

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 (under observation or inpatient status) with bronchiolitis at one of three study sites
  • Physicians and advanced practice providers entering the patient's chart or orders entry activity for Emergency Department and inpatient encounters
Not Eligible

You will not qualify if you...

  • Current encounter is a birth encounter
  • Currently hospitalized in an intensive care unit (ICU)
  • Hospitalized with length of stay longer than 14 days
  • Physicians and advanced practice providers who do not enter the patient's chart or orders entry activity

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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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

C

Clea D Harris, MD

CONTACT

B

Benjamin Bodnar, MD

CONTACT

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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