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Clinical Trials/NCT03736603
NCT03736603
Completed
Not Applicable

The PIPA Study (Pathways for Improving Pediatric Asthma Care): A Cluster Randomized Trial

University of California, San Francisco1 site in 1 country303 target enrollmentJanuary 1, 2018
ConditionsAsthma

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Asthma
Sponsor
University of California, San Francisco
Enrollment
303
Locations
1
Primary Endpoint
Hospital/Inpatient: Mean length of hospital stay
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

Background:

Asthma affects nearly 10% of American children, and is a leading cause of pediatric emergency visits and hospitalizations. Clinical pathways are operational versions of practice guidelines aimed at the hospital management of common illnesses. Single-site studies of pediatric asthma pathways have shown significant improvements in quality of care.

Primary Objective:

To evaluate the effectiveness of clinical pathways for improving quality of care for children with asthma in a diverse, national sample of emergency department (ED) and hospital settings.

Primary Endpoints:

  1. Emergency Department: The proportion of eligible children who receive systemic steroids within 60 minutes of ED arrival
  2. Inpatient/Hospital: Mean length of hospital stay

Study Design:

This project will be implemented through an established quality improvement collaborative of hospitals across the United States, the Value in Inpatient Pediatrics Network (part of the American Academy of Pediatrics). A cluster randomized design will be employed. Group 1 hospitals will receive a multifaceted implementation strategy that includes: 1) a pathway implementation toolkit, 2) local multidisciplinary champions in the ED and inpatient settings, 3) audit and feedback, 4) educational seminars, and 5) practice facilitation (via teleconference). Group 2 will receive the same intervention with the addition of a mobile app pathway tool.

Registry
clinicaltrials.gov
Start Date
January 1, 2018
End Date
June 30, 2019
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Working as a physician at the study site

Exclusion Criteria

  • Patient/child eligibility criteria:
  • Inclusion Criteria:
  • Age 2-17 years
  • Primary diagnosis of asthma
  • Exclusion Criteria:
  • Transferred in from another inpatient facility
  • Presence of a chronic medical condition that precludes pathway use

Outcomes

Primary Outcomes

Hospital/Inpatient: Mean length of hospital stay

Time Frame: 1 year

Emergency Department: Proportion of eligible children who receive systemic steroids within 60 minutes of ED arrival

Time Frame: 1 year

Secondary Outcomes

  • Hospital/Inpatient: Proportion of children screened for secondhand tobacco smoke exposure(1 year)
  • Hospital/Inpatient: Proportion of children prescribed antibiotics at hospital discharge(1 year)
  • Hospital/Inpatient: Proportion of children with administration of bronchodilator via metered-dose inhaler early in hospitalization(1 year)
  • Hospital/Inpatient: Proportion of children with emergency department visits or readmissions to the hospital within 7 days(1 year)
  • Emergency Department: Proportion of children who get an asthma exacerbation severity assessment at ED triage(1 year)
  • Emergency Department: Proportion of children who have chest radiographs performed(1 year)
  • Hospital/Inpatient: Proportion of children who screen positive for secondhand tobacco smoke exposure whose caregivers are referred to smoking cessation resources(1 year)
  • Hospital/Inpatient: Proportion of children transferred to a higher level of care(1 year)
  • Emergency Department: Proportion of children transferred to a higher level of care(1 year)
  • Emergency Department: Proportion of children admitted to the hospital(1 year)
  • Emergency Department: Mean length of emergency department stay(1 year)

Study Sites (1)

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