Targeted Feedback Reports to Improve Acute Coronary Syndromes (ACS) Care
Primary Purpose
Acute Coronary Syndromes
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Targeted Feedback Reports
Targeted Feedback Report
Sponsored by
About this trial
This is an interventional health services research trial for Acute Coronary Syndromes focused on measuring quality improvement
Eligibility Criteria
Inclusion Criteria:
- hospitals participating in the ACTION Registry GWTG
Exclusion Criteria:
- sites with low volume of data submission (< 10 data forms in the past year)
Sites / Locations
- Duke University Health System
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Targeted Feedback Reports
Targeted Feedback Report
Arm Description
Conventional feedback reports
Report designed to target areas for local hospital-specific improvement.
Outcomes
Primary Outcome Measures
The primary outcome is improvement in the overall composite of all metrics eligible for intervention regardless of their selection as targets.
Secondary Outcome Measures
The secondary outcome is improvement in the composite of targeted metrics.
Full Information
NCT ID
NCT00952250
First Posted
August 4, 2009
Last Updated
December 1, 2011
Sponsor
Duke University
Collaborators
Agency for Healthcare Research and Quality (AHRQ)
1. Study Identification
Unique Protocol Identification Number
NCT00952250
Brief Title
Targeted Feedback Reports to Improve Acute Coronary Syndromes (ACS) Care
Official Title
Personalized and Targeted Feedback in the ACTION-Registry-GWTG
Study Type
Interventional
2. Study Status
Record Verification Date
December 2011
Overall Recruitment Status
Completed
Study Start Date
February 2009 (undefined)
Primary Completion Date
July 2011 (Actual)
Study Completion Date
July 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Duke University
Collaborators
Agency for Healthcare Research and Quality (AHRQ)
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This project is designed to examine the impact of tailored feedback on site performance.
The investigators' objective is to evaluate whether a 'personalized and targeted' feedback, education and performance improvement intervention has a greater impact on adherence to recommended guidelines than standard feedback.
The investigators hypothesize that a site-specific report with centrally identified targets for improvement paired with target specific interventions will enable sites to quickly identify and prioritize salient problem areas, have ready access to an analysis of factors that underlie problems, and formulate an effective action plan. The investigators also hypothesize that those hospitals randomized to receive intervention will be more likely to improve their overall performance, as well as their target specific performance, during the period of observation in direct response to activated QI processes.
Outcomes:
The primary outcome is improvement in the overall composite of all metrics eligible for intervention regardless of their selection as targets.
The secondary outcome is improvement in the composite of targeted metrics.
Outcomes will be assessed in all participating sites, and in among relevant performance subgroups (low performers, academic centers, full service, and among medication versus process metrics).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Coronary Syndromes
Keywords
quality improvement
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
149 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Targeted Feedback Reports
Arm Type
Active Comparator
Arm Description
Conventional feedback reports
Arm Title
Targeted Feedback Report
Arm Type
Experimental
Arm Description
Report designed to target areas for local hospital-specific improvement.
Intervention Type
Behavioral
Intervention Name(s)
Targeted Feedback Reports
Intervention Description
Sites randomized to this arm will receive specialized feedback summarizing their adherence to the guidelines and suggestions on ways to improve performance.
Intervention Type
Behavioral
Intervention Name(s)
Targeted Feedback Report
Intervention Description
Report designed to target areas for local hospital-specific improvement
Primary Outcome Measure Information:
Title
The primary outcome is improvement in the overall composite of all metrics eligible for intervention regardless of their selection as targets.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
The secondary outcome is improvement in the composite of targeted metrics.
Time Frame
12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
hospitals participating in the ACTION Registry GWTG
Exclusion Criteria:
sites with low volume of data submission (< 10 data forms in the past year)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Karen P Alexander, MD
Organizational Affiliation
Duke University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Duke University Health System
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27705
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
21245461
Citation
Alexander KP, Wang TY, Li S, Lytle BL, Slattery LE, Calhoun S, Poteat J, Roe MT, Rumsfeld JS, Cannon CP, Peterson ED. Randomized trial of targeted performance feedback to facilitate quality improvement in acute myocardial infarction care. Circ Cardiovasc Qual Outcomes. 2011 Jan 1;4(1):129-35. doi: 10.1161/CIRCOUTCOMES.110.958470.
Results Reference
derived
Learn more about this trial
Targeted Feedback Reports to Improve Acute Coronary Syndromes (ACS) Care
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