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Clinical Trials/NCT05923463
NCT05923463
Active, not recruiting
Not Applicable

A Scalable Service to Improve Health Care Quality Through Precision Audit and Feedback: a Cluster-randomized Controlled Trial

University of Michigan1 site in 1 country3,500 target enrollmentMay 6, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Anesthesia Care Quality
Sponsor
University of Michigan
Enrollment
3500
Locations
1
Primary Endpoint
Measure success rate (M) for operative cases of anesthesia care providers
Status
Active, not recruiting
Last Updated
last year

Overview

Brief Summary

This cluster-randomized trial will assess the effectiveness of a precision feedback service on anesthesia provider performance. The precision feedback service enhances a standard audit and feedback (A&F) email with a brief message and visual display about high-value performance information. The control arm will receive a standard "one size fits most" A&F email that is currently sent to anesthesia providers each month. Hypothesis: Providers receiving precision feedback will increase a) care quality for improvable measures and b) email engagement (click-through and dashboard login rates) when compared with providers receiving standard A&F emails. The study investigators will assess unintended consequences in a mixed-methods process evaluation.

Registry
clinicaltrials.gov
Start Date
May 6, 2024
End Date
June 2025
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Zach Landis-Lewis

Assistant Professor of Learning Health Sciences

University of Michigan

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Measure success rate (M) for operative cases of anesthesia care providers

Time Frame: Up to 1 year

The primary outcome for the cluster-randomized controlled trial is the measure success rate (M) for operative cases of anesthesia care providers, where: M = sum of all operative case measurement successes / number of all operative case measurements The measures included in each provider's measure success rate will be all improvable process measures that meet the following inclusion criteria: 1. A provider's cases were included for the measure during both the 6-month pre-intervention period and during the 6-month intervention period. 2. Average performance for the measure is below 90% during the baseline period, based on the MPOG threshold for most process measures. 3. The measure was included in at least one provider feedback email during the intervention period. The investigators will exclude measures of clinical outcomes (also called "inverse measures") in this study that are less within the control of providers.

Secondary Outcomes

  • Average email click-through rate (CTR)(Up to 6 months)
  • Average dashboard login rate (L)(Up to 1 year)

Study Sites (1)

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