- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02593253
The Effect of a Novel Audit and Feedback Bundle on Inpatient Performance
May 5, 2017 updated by: University of California, San Francisco
The Effect of a Novel Electronic Physician Audit and Feedback Bundle on Inpatient Performance Metrics
This single-blinded, cluster randomized control trial will assess the effectiveness of an audit and feedback bundle on internal medicine physician performance on selected quality metrics.
The feedback bundle includes an electronic dashboard and weekly feedback rounds in which physicians will review their performance.
The control arm will undergo audit and feedback per the current system, which is biweekly feedback emails with performance.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This is a single-blinded, cluster randomized control trial of 48 internal medicine teams (24 teams will be randomized to the intervention arm and and 24 teams randomized to control arm) on inpatient medicine wards.
Each team consists of at least 4 members (attending physician, senior resident, two interns).
The intervention arm teams will receive the new audit and feedback bundle, which includes access to the electronic dashboard and weekly feedback rounds in which they review their performance on several inpatient quality metrics via the electronic dashboard.
The control arm will undergo audit and feedback per the current system, which is biweekly feedback emails with performance on selected quality measures.
This primary aim of the trial will be to compare the effectiveness of performance feedback on inpatient quality metrics specifically high quality after visit summary, medical reconciliation and discharge summary timeliness.
Other group comparisons will include other inpatient quality metrics and satisfaction with feedback.
Study Type
Interventional
Enrollment (Actual)
200
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
California
-
San Francisco, California, United States, 94143
- University of California San Francisco
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- All physicians that rotate through internal medicine wards during the study period (teaching attending physicians and internal medicine residents and interns)
Exclusion Criteria:
- None
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Intervention Audit and Feedback Bundle
Access to the electronic dashboard and weekly feedback rounds
|
The intervention arm teams will receive the new audit and feedback bundle, which includes access to the electronic dashboard and weekly feedback rounds in which they review their performance on several inpatient quality metrics via the dashboard.
|
Active Comparator: Bi-weekly audit and feedback emails
Access to biweekly feedback emails with performance on selected quality measures (current practice).
|
The control arm will undergo audit and feedback per the current system, which is biweekly feedback emails with performance on selected quality measures.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Proportion of patients with a high quality after visit summary
Time Frame: 6 months
|
The number of hospital medicine team patients with after visit summaries of high quality divided by the total number hospital medicine team patients with an after visit summary.
|
6 months
|
Proportion of patients with discharge summary timeliness
Time Frame: 6 months
|
The number of discharge summaries completed within 24 hours of discharge for hospital medicine team patients/total number of discharges from hospital medicine with a discharge summary completed
|
6 months
|
Proportion of patients Complete Medication Reconciliation by Discharge
Time Frame: 6 months
|
The total number of patients with an action taken on all home medications divided by the total number of patients on the hospital medicine teaching service.
|
6 months
|
Proportion of patients achieving a high quality 'perfect' discharge
Time Frame: 6 months
|
Proportion of patients who have a high quality after visit summary and a discharge summary completed within 24 of discharge and all medications reconciled by discharge.
|
6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Proportion of attending and resident physicians who 'strongly agree' that they are satisfied with the audit and feedback of performance data that they receive.
Time Frame: 6 months
|
Proportion of attending and resident physicians who 'strongly agree' that they are satisfied with the audit and feedback of performance data that they receive.
This specific satisfaction item has been developed by the study team.
|
6 months
|
Total Phlebotomy Sticks
Time Frame: 6 months
|
The total number of unique accession numbers for each unique hospitalization of a patient
|
6 months
|
Percent of Patients on Telemetry Until Discharge
Time Frame: 6 months
|
The number of patients on without a discontinue order for telemetry within two hours of their discharge date time divided by the total number of patients on telemetry for hospital medicine teams
|
6 months
|
Proportion of patients discharged by noon
Time Frame: 6 months
|
The number of patients discharged by hospital medicine team attendings by noon (6am-11:59am)/total number of discharges by hospital medicine team attendings
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Alvin R Rajkomar, MD, University of California, San Francisco
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 1, 2016
Primary Completion (Actual)
December 1, 2016
Study Completion (Actual)
May 1, 2017
Study Registration Dates
First Submitted
October 23, 2015
First Submitted That Met QC Criteria
October 29, 2015
First Posted (Estimate)
November 1, 2015
Study Record Updates
Last Update Posted (Actual)
May 9, 2017
Last Update Submitted That Met QC Criteria
May 5, 2017
Last Verified
May 1, 2017
More Information
Terms related to this study
Other Study ID Numbers
- 15-17709
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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