Reduction in Clinical Variance Using Targeted Design Changes in Computerized Provider Order Entry Order (CPOE) Sets
1 other identifier
interventional
458
1 country
1
Brief Summary
Selective redesign of order sets using different ways to frame the order and physician decision-making in a computerized provider order entry system could increase adherence to evidence-based care and reduce population-specific variance.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for phase_3
Started Sep 2004
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2004
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2006
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2006
CompletedFirst Submitted
Initial submission to the registry
July 24, 2009
CompletedFirst Posted
Study publicly available on registry
August 6, 2009
CompletedMay 21, 2015
May 1, 2015
2.2 years
July 24, 2009
May 19, 2015
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Reduced variation from in evidence-based care through integrating evidence into the clinician workflow in the EMR system.
2 years
Study Arms (2)
Baseline Period
NO INTERVENTIONPatients in the baseline period were cared for using the standard historical electronic order set.
Post Intervention Period
ACTIVE COMPARATORPatients in the Post intervention period were cared for with evidence-bsed modified order set changes
Interventions
The order set was altered to include evidence based care items
Eligibility Criteria
You may qualify if:
- All patients admitted using an acute asthma exacerbation order set.
You may not qualify if:
- Patients who did not have either an admission or discharge diagnosis of asthma exacerbation.
- In addition, patients admitted to the intensive care unit directly or transferred to the intensive care unit within 24-hours were excluded from analysis.
- Finally, patients were excluded from analysis if asthma was not the presenting problem.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Brian Jacobslead
- Siemens Medicalcollaborator
Study Sites (1)
Cincinnati Children's Hospital Medical Center
Cincinnati, Ohio, 45229, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- phase 3
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- FACTORIAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- MD
Study Record Dates
First Submitted
July 24, 2009
First Posted
August 6, 2009
Study Start
September 1, 2004
Primary Completion
December 1, 2006
Study Completion
December 1, 2006
Last Updated
May 21, 2015
Record last verified: 2015-05