ClinicalTrials.gg
Active, not recruitingNCT07334795SCORE-PedsUpdated Mar 27, 2026

Intermountain Stewardship in Community Outpatient Settings-Resources & Engagement-Pediatrics

An observational study in Respiratory Infection (for Example, Pneumonia, Bronchitis), Antibiotic and Antibiotic Duration, sponsored by Intermountain Health Care, Inc.. Active, not recruiting at 1 site in United States. Open to participants aged 6 Months to 17 Years. Per ClinicalTrials.gov, last updated 2026-03-27.

Sponsored by Intermountain Health Care, Inc. · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
259,000
Ages
6 Months to 17 Years
Sex
All
01

Study summary

The goal of this implementation project is to detail the process of implementing the best practice of antibiotic stewardship in the pediatric population across the Intermountain Health medical system. The main questions it aims to answer are:

  • How can a large healthcare system drive high adherence to antibiotic stewardship across a large and diverse number of sites?
  • How do determinants of implementation and needed strategies vary by context?
  • What is the utility of a higher-resource implementation effort (named "Boost) focusing on outlier sites?

Data will be collected on number of children reached, adherence changes over time, types of implementation strategies employed, and characteristics of sites, prescribers, and patients.

02

Conditions studied

  • Respiratory Infection (for Example, Pneumonia, Bronchitis)
  • Antibiotic
  • Antibiotic Duration
  • Antibiotic Prescribing for Acute Respiratory-tract Infections
03

In context

Respiratory Tract Infections

751 studies on the registry are indexed under Respiratory Tract Infections; 114 are open to participants now.

This study's planned enrollment of 259,000 is above the median of 350 across 184 observational studies indexed under Respiratory Tract Infections.

Browse Respiratory Tract Infections studies →

Lead sponsor

Intermountain Health Care, Inc. is the lead sponsor of 120 studies on the registry; 15 are open to participants now.

Of its 9 completed or terminated interventional studies of FDA-regulated products, 3 (33%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
6 Months to 17 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

All children meeting eligibility criteria and treated at any facility within the Intermountain region specified (wave 1 \& wave 2) between January 1, 2026 and December 31, 2028.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age 6 months through 17 years
  • ARTI diagnosis (acute otitis media (AOM), Group A Streptococcal (GAS) pharyngitis, acute sinusitis, and community-acquired pneumonia (CAP))

Exclusion criteria

Exclusion Criteria:

  • Age \<6months or >18 years
  • No ARTI diagnosis
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
259,000 participants (estimated)
Patient registry
No

Groups and cohorts

  • Children with ARTIs, Wave 1

    Children under 18 treated in Wave 1 of antibiotic stewardship for the following conditions: acute otitis media (AOM), Group A Streptococcal (GAS) pharyngitis, acute sinusitis, and community-acquired pneumonia (CAP)

    Other: Implementation strategies including training & education, EMR tools, audit & feedback reports, and facilitation

  • Children with ARTIs, Wave 2

    Children under 18 treated in Wave 2 of antibiotic stewardship for the following conditions: acute otitis media (AOM), Group A Streptococcal (GAS) pharyngitis, acute sinusitis, and community-acquired pneumonia (CAP)

    Other: Implementation strategies including training & education, EMR tools, audit & feedback reports, and facilitation

Interventions

  • OtherImplementation strategies including training & education, EMR tools, audit & feedback reports, and facilitation

    o facilitate improved adherence to guideline-based prescribing, we plan a variety of implementation strategies to be employed in tandem including training \& education, EMR tools (e.g., Smart sets, express lanes, preference lists), audit and feedback reports and dashboards, and facilitation.

06

What researchers measure

Primary outcomes

  1. Guideline-adherent Broad vs. Narrow Spectrum Antibiotic Prescribing

    Rates of narrow-spectrum antibiotic (AB) prescriptions as a proportion of all antibiotics prescribed in aggregate and within each of these diagnoses: Acute otitis media, Group A streptococcal pharyngitis, Acute sinusitis, and Pneumonia.

    Time frame: Baseline month adherence and post implementation (12 months). Maintenance period is 6 months post implementation.

  2. Guideline-adherent Duration of Antimicrobial Therapy

    Rate of AB prescriptions with guideline-adherent number of days prescribed as proportion of all AB prescriptions in aggregate and for each of the target ARTI diagnoses.

    Time frame: Baseline month adherence and post implementation (12 months). Maintenance period is 6 months post implementation.

Secondary outcomes

  1. Rate of Treatment Failure

    Clinical encounter for the same diagnosis between 2 and 14 days following the index encounter and receipt of an alternative antibiotic for the same respiratory diagnosis during the return visit.

    Time frame: Baseline month adherence and post implementation (12 months). Maintenance period is 6 months post implementation

  2. Adoption (Staff): Adherence to Protocols

    Number and proportion of prescribers who are "adherent" to guideline-based prescribing protocols for Broad vs. Narrow Spectrum AB Prescribing, and Duration.

    Time frame: Baseline month adherence and post implementation (12 months). Maintenance period is 6 months post implementation

  3. Adoption (Organization): Adherence to Protocols

    Number and proportion of sites where 60% of prescribers are adherent.

    Time frame: Baseline month adherence and post implementation (12 months). Maintenance period is 6 months post implementation.

07

Study locations

1 site
08

References and documents

Publications

  • Fowles TR, Patel PK, Seibert AM, Hersh AL, Belnap T, Hanna B, Szymczak JE, Keenan HT, Barney BJ, Srivastava R. Implementation of a pediatric antibiotic stewardship intervention across a large integrated health system: protocol to optimize antibiotic selection and prescription duration for acute respiratory tract infections in children. Implement Sci Commun. 2026 Apr 9;7(1):93. doi: 10.1186/s43058-026-00915-0. PubMed 41952161 ↗

Individual participant data

Plan to share: No — This is an implementation study using observational data with a waiver of consent. Therefore, there is no consent to allow for the sharing of IPD.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Jan 2026 (actual). Primary completion is estimated for Jan 2029, 36 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Dec 31, 2025
First posted
Jan 12, 2026
StartActual
Jan 15, 2026
Primary completionEst.
Jan 15, 2029
CompletionEst.
Jan 15, 2029
Last update
Mar 27, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Mar 27, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07334795
Responsible party
Sponsor
First posted
Jan 12, 2026
Start date
Jan 15, 2026
Primary completion
Jan 15, 2029 (estimated)
Completion
Jan 15, 2029 (estimated)
Last update
Mar 27, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Oct 2025. You cannot join it, but the record below documents what was studied.

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