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OpenTrials
Completed

NCT Number: NCT00952471

Reduction in Clinical Variance Using Targeted Design Changes in Computerized Provider Order Entry Order (CPOE) Sets

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.

Completed

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Cincinnati Children's Hospital Medical Center

Cincinnati, Ohio, 45229, United States

About this study

Variance in ordering of care can be characterized as the lack of uniform use of specific treatments by clinicians for a given medical condition. Unwarranted variance in healthcare has been associated with prolonged length of stay, diminished health and increased cost. Practice variation in the management of asthma can be significant and few investigators have evaluated strategies to reduce this variation. We hypothesized that 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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All patients admitted using an acute asthma exacerbation order set.

Exclusion criteria

  • 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.

Treatment and study plan

Evidence Based Intervention to order set

Other

The order set was altered to include evidence based care items

Primary outcomes

  1. Reduced variation from in evidence-based care through integrating evidence into the clinician workflow in the EMR system.

    Time frame: 2 years

Sponsors and collaborators

Lead sponsor

Brian Jacobs

Other

Collaborators

  • Siemens Medical

Registry information

Important dates

Study start
2004
Primary completion
2006
Study completion
2006
First posted
Aug 6, 2009
Registry last updated
May 21, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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