Stroger Hospital of Cook County
Chicago, Illinois, 60612, United States
NCT Number: NCT00930111
The investigators are testing the effects of a change in teaching attending physicians' rotations (from 4- to 2-week blocks) on patient outcomes (unplanned urgent visits to the health care system, inpatient mortality, and length-of-stay), the educational experiences of residents and medical students and on the quality of the professional lives of the attending physicians.
Looking for future studies?
Notify MeAll sexes
Interventional
Not applicable
Chicago, Illinois, 60612, United States
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Attending physician is assigned to a 2-week rotation.
Attending physician is assigned to a 4-week rotation.
Time frame: 30 days after discharge
Number pf non-scheduled patient encounters documented in the EHR
Time frame: During 14 or 28 day rotations
Self administered performance electronic evaluations - validated tool
Time frame: During 14 or 28 day rotations
Self administered performance electronic evaluations
Time frame: During and 14 to 28 days after provider's rotation
Number pf non-scheduled patient encounters documented in the EHR
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.
Pamela Gonzalez Sr Director Clinical Research Office
Other Gov
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.
Published trials that share one or more normalized conditions with this study.
NCT07648576
Anxiety Disorders, Behavior
Bursa, Turkey (Türkiye)
View Trial DetailsNCT07647159
Behavior, Behavioral Symptoms
Moscow, Russia
View Trial DetailsNCT05677997
Behavior, Behavioral Symptoms
Toronto, Ontario, Canada
View Trial DetailsNCT05582343
Behavior, Behavioral Symptoms
Columbus, Ohio, United States
View Trial Details