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A Pragmatic Cluster Randomized Controlled Trial to Standardize Attending Morning Rounds in Medicine

Not Applicable
Completed
Conditions
Inpatients
Quality Improvement
Morning Rounds
Hospitalization
Teaching Rounds
Interventions
Other: Standardized attending morning rounds
Registration Number
NCT01931553
Lead Sponsor
University of California, San Francisco
Brief Summary

Attending morning rounds take place at teaching hospitals every day. They are the primary mechanism for patient care delivery, supervision and education of trainees, and communication with patients, families, and staff. However, they are done with little standardization or widely recognized best practices.

The objective of this quality improvement (QI) initiative is to evaluate the adherence to and impact of implementing standardized attending morning rounds on medicine teams at our institution. A standardized rounding intervention has been developed which includes specific guidance on completing the following activities during morning rounds: (1) Pre-rounds discretion; (2) Pre-rounds huddle; (3) Bedside registered nurse (RN) integration; (4) Patient-centered rounding; (5) Real-time order writing.

This trial will randomize half of the investigators' medicine teams at University of California San Francisco to this rounding intervention whilst the other half will be randomized to continue with usual unstandardized rounding practices.

The investigators will compare medicine teams randomized to undertake standardized rounding to those teams undertaking usual practice. Outcomes assessed will relate to the patient (e.g. satisfaction), providers (e.g. satisfaction), efficiency (e.g. total morning round time) as well as adherence to the intervention .

The investigators' study hypotheses are that patient satisfaction scores will be higher for those patients receiving standardized bedside rounds compared to the usual care group. The investigators also hypothesize that total attending morning rounds time and interns length of workday will be shorter and that the number of consultations ordered before noon will increase for those teams undertaking standardized bedside. Further, the investigator hypothesize higher levels of nurse participation, physician and medical student satisfaction with standardized bedside rounding.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
1200
Inclusion Criteria
  • All attending physicians, residents, interns and medical students of Medicine teams A through H
  • All patients admitted to Medicine teams A through H
  • All nurses on the Medicine floors
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Exclusion Criteria
  • None
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Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Standardized attending morning roundsStandardized attending morning rounds1. Pre-rounds discretion 2. Pre-rounds huddle 3. Bedside RN integration 4. Patient-centered rounding 5. Real-time order writing
Primary Outcome Measures
NameTimeMethod
Patient satisfaction with provider communicationOnce, within one month of hospital discharge

Post-discharge assessment will be sent by a commercial Vendor (Press Ganey) within a month of discharge following hospitalization

Patient satisfaction with morning roundsOnce, after day one of hospitalization and before patient is discharged.

Patient satisfaction with morning ward rounds. This inpatient assessment will occur after day one of hospitalization before the patient is discharged from hospital. This time point will ensure that patients have experienced rounds at least once before completing a patient satisfaction survey.

Secondary Outcome Measures
NameTimeMethod
Interns total length of workdayDaily during the 3-month trial

The interns total length of workday will be recorded daily. Over the course of the trial the average length of workday will be determined including any duty hour violations.

Number of consultations ordered before noonDaily during the 3-month trial

The number of consultations ordered before noon will be recorded daily. Over the course of the trial the average number of consultations ordered before noon will be calculated.

Resident satisfactionOnce during the last week of their rotation on a given team

Resident satisfaction and perceptions of with morning rounds (e.g. efficiency, organization, educational value)

Attending physician satisfactionOnce during the last week of their rotation on a given team

Attending physician satisfaction and perceptions of with morning rounds (e.g. efficiency, organization, educational value)

Medical student satisfactionOnce during the last week of their rotation on a given team

Medical student satisfaction and perceptions of with morning rounds (e.g. efficiency, organization, educational value)

Total morning rounding timeDaily during the 3-month trial

Total morning rounding time will be recorded daily for each team. Over the course of the trial the average length of morning rounds will be determined.

Nurse participation in morning roundsDaily during the 3-month trial

The presence of RN during morning ward rounds will be recorded daily.

Nurse satisfactionOnce during the last week the trial

Nurse satisfaction and perceptions of with morning rounds (e.g. efficiency, organization, team work)

Intern satisfactionOnce during the last week of their rotation on a given team

Intern satisfaction and perceptions of with morning rounds (e.g. efficiency, organization, educational value)

Trial Locations

Locations (1)

University of California San Francisco Medical Center

🇺🇸

San Francisco, California, United States

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