- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00930111
Inpatient Attending Physician Rotation Duration Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Design, Setting, and Participants Cluster randomized crossover noninferiority trial, with attending physicians as the unit of crossover randomization and 4-week rotations as the active control, conducted in a US university-affiliated teaching hospital in academic year 2009. Participants were 62 attending physicians who staffed at least 6 weeks of inpatient service, the 8892 unique patients whom they discharged, and the 147 house staff and 229 medical students who evaluated their performance.
Intervention Assignment to random sequences of 2- and 4-week rotations.
Main Outcome Measures Primary outcome was 30-day unplanned revisits (visits to the hospital's emergency department or urgent ambulatory clinic, unplanned readmissions, and direct transfers from neighboring hospitals) for patients discharged from 2- vs 4-week within-attending-physician rotations. Noninferiority margin was a 2% increase (odds ratio [OR] of 1.13) in 30-day unplanned patient revisits. Secondary outcomes were length of stay; trainee evaluations of attending physicians; and attending physician reports of burnout, stress, and workplace control.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Illinois
-
Chicago, Illinois, United States, 60612
- Stroger Hospital of Cook County
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Attending physician on inpatient general medicine wards of Stroger Hospital, Chicago, IL
Exclusion Criteria:
- Scheduled for less than 6 weeks during the 2009 academic year
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: 2 weeks
Attending physicians are physician-of-records for traditional inpatient ward team (housestaff and medical students) for 2 weeks.
|
Attending physician is assigned to a 2-week rotation.
|
Placebo Comparator: 4 weeks
Attending physicians are physician-of-records for traditional inpatient ward team (housestaff and medical students) for 4 weeks.
|
Attending physician is assigned to a 4-week rotation.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Patients' unplanned urgent visits to the health care system.
Time Frame: 30 days after discharge
|
Number pf non-scheduled patient encounters documented in the EHR
|
30 days after discharge
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Resident physicians' evaluation of attending physicians' performance.
Time Frame: During 14 or 28 day rotations
|
Self administered performance electronic evaluations - validated tool
|
During 14 or 28 day rotations
|
Medical students' evaluations of attending physicians' performance.
Time Frame: During 14 or 28 day rotations
|
Self administered performance electronic evaluations
|
During 14 or 28 day rotations
|
Urgent visits to health care system among attending physicians' outpatient panel (if attending physician has an outpatient panel)
Time Frame: During and 14 to 28 days after provider's rotation
|
Number pf non-scheduled patient encounters documented in the EHR
|
During and 14 to 28 days after provider's rotation
|
Attending physicians' work-life balance, perceived stress, and perceived burn-out.
Time Frame: During 14 to 28 day rotations
|
Self administered confidential Burnout assessment survey based on Conceptual Model of Burnout, Perceived Stress Scale & Maslach Burnout Inventory Human ServiceSurvey and a single item measure from the Notional Job Burnout Survey.
|
During 14 to 28 day rotations
|
Collaborators and Investigators
Investigators
- Principal Investigator: Brian Lucas, MD, Cook County Health
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 09-063 Cooker 533
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.
Clinical Trials on Inpatient Attending Physician Staffing Model
-
Ohio State UniversityCompletedOutpatient | Physician-Patient Relations | Inpatient Facility Diagnoses | Electronic Health RecordsUnited States
Clinical Trials on 2-week rotation
-
Yorkshire Ambulance Service NHS TrustApplied Research Collaboration for Yorkshire and HumberUnknownSafe Paramedic Non-conveyanceUnited Kingdom
-
Postgraduate Institute of Medical Education and...RecruitingBreast Cancer | Radiotherapy Side Effect | HypofractionationIndia
-
University of MiamiCompletedDepression | Anxiety | Cognitive Change | Post Traumatic Stress Disorder | Psychological StressUnited States
-
Peking UniversityCenters for Disease Control and Prevention, China; Beijing Pinggu District... and other collaboratorsCompleted
-
Somogy Megyei Kaposi Mór Teaching HospitalCompleted
-
University of Colorado, DenverCompletedShoulder DislocationUnited States
-
University of TwenteCompleted
-
Seoul National University HospitalCompletedLaryngeal InjuriesKorea, Republic of
-
International Centre for Diarrhoeal Disease Research...Completed