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Completed

NCT Number: NCT00930111

Inpatient Attending Physician Rotation Duration Study

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.

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Stroger Hospital of Cook County

Chicago, Illinois, 60612, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

2-week rotation

Other

Attending physician is assigned to a 2-week rotation.

4-week rotation

Other

Attending physician is assigned to a 4-week rotation.

Primary outcomes

  1. 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

Secondary outcomes

  1. Resident physicians' evaluation of attending physicians' performance.

    Time frame: During 14 or 28 day rotations

    Self administered performance electronic evaluations - validated tool

  2. Medical students' evaluations of attending physicians' performance.

    Time frame: During 14 or 28 day rotations

    Self administered performance electronic evaluations

  3. 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

  4. 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.

Sponsors and collaborators

Lead sponsor

Pamela Gonzalez Sr Director Clinical Research Office

Other Gov

Registry information

Important dates

Study start
2009
Primary completion
2010
Study completion
2010
First posted
Jun 30, 2009
Registry last updated
Jul 11, 2023

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.

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