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I-DECIDE After Bronchiolitis Hospitalization
NCT07243652 · View on ClinicalTrials.gov ↗
Study Summary
Although automatic follow-up is a nearly universal practice, research has shown that these visits are often unnecessary after hospitalizations caused by bronchiolitis. Despite endorsement by national pediatric authorities, robust evidence, and family enthusiasm for as-needed (PRN) follow-up, it remains substantially underutilized for children hospitalized for bronchiolitis. The goal of I-DECIDE is to compare the effects of two multi-component implementation strategies, both of which aim to (a) increase PRN follow-up prescribing by hospitalists (physicians who care for hospitalized children) and (b) decrease unnecessary follow-up visit attendance by families.
Conditions Studied
Interventions
- OTHER Moderate-Resource Implementation Strategy
- OTHER High-Resource Implementation Strategy
Study Locations (20)
California
- Adventist Health Lodi Memorial — Lodi
- Children's Hospital Los Angeles — Los Angeles
- Valley Children's Hospital — Madera
- Children's Hospital Orange County (CHOC) — Orange
- University of California Davis Children's Hospital — Sacramento
Arizona
- Phoenix Children's Hospital - Arrowhead Campus — Glendale
- Phoenix Children's Hospital — Phoenix
Connecticut
- Connecticut Children's Medical Center — Hartford
- Yale-New Haven Children's Hospital — New Haven
Illinois
- Ann & Robert H. Lurie Children's Hospital of Chicago — Chicago
- OSF Children's Hospital of Illinois — Peoria
Massachusetts
- Boston Children's Hospital — Boston
- Baystate Children's Hospital — Springfield
Alabama
- Children's of Alabama — Birmingham
Colorado
- Children's Hospital Colorado — Aurora
District of Columbia
- Children's National Medical Center — Washington D.C.
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 2,700 participants |
| Start Date | 2025-11-01 |
| Est. Completion | 2029-12 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07243652
The ClinicalTrials.gov registry entry for NCT07243652 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 2,700 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Seattle Children's Hospital, which has 127 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Bronchiolitis Acute appearing as the primary indexed condition, and to 2 interventions — of which Moderate-Resource Implementation Strategy is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT07243652 reports 20 study locations spanning 12 distinct geographic areas — top geographies include California, Arizona, Connecticut. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT07243652 about?
NCT07243652 is a clinical study titled "I-DECIDE After Bronchiolitis Hospitalization". Although automatic follow-up is a nearly universal practice, research has shown that these visits are often unnecessary after hospitalizations caused by bronchiolitis. Despite endorsement by national pediatric authorities, robust evidence, and family enthusiasm for as-needed (PRN) follow-up, it rema...
What is the current status of trial NCT07243652?
This trial is currently recruiting. It is a NA study. The enrollment target is 2,700 participants. The study started on 2025-11-01. Estimated completion is 2029-12.
What conditions does trial NCT07243652 study?
This clinical trial studies the following conditions: Bronchiolitis Acute. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT07243652?
The interventions under investigation include: Moderate-Resource Implementation Strategy (OTHER), High-Resource Implementation Strategy (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT07243652?
This trial is sponsored by Seattle Children's Hospital, which has 127 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT07243652 being conducted?
This trial has 20 study locations across Alabama, Arizona, California, Colorado, Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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