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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01931553
Enrollment
1200
Registered
2013-08-29
Start date
2013-09-30
Completion date
2014-12-31
Last updated
2015-05-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hospitalization, Inpatients, Morning Rounds, Quality Improvement, Teaching Rounds

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.

Interventions

OTHERStandardized attending morning rounds

Sponsors

University of California, San Francisco
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frameDescription
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.
Patient satisfaction with provider communicationOnce, within one month of hospital dischargePost-discharge assessment will be sent by a commercial Vendor (Press Ganey) within a month of discharge following hospitalization

Secondary

MeasureTime frameDescription
Resident satisfactionOnce during the last week of their rotation on a given teamResident 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 teamAttending physician satisfaction and perceptions of with morning rounds (e.g. efficiency, organization, educational value)
Nurse participation in morning roundsDaily during the 3-month trialThe presence of RN during morning ward rounds will be recorded daily.
Nurse satisfactionOnce during the last week the trialNurse 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 teamIntern satisfaction and perceptions of with morning rounds (e.g. efficiency, organization, educational value)
Total morning rounding timeDaily during the 3-month trialTotal 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.
Medical student satisfactionOnce during the last week of their rotation on a given teamMedical student satisfaction and perceptions of with morning rounds (e.g. efficiency, organization, educational value)
Interns total length of workdayDaily during the 3-month trialThe 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 trialThe 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.

Other

MeasureTime frameDescription
30-day readmission rateFor entire 3 month study periodAverage readmission rate for each group for entire 3-month study period
Adherence to the interventionDaily during the 3-month trialAdherence to the standardized intervention will be recorded throughout the trial to determine the uptake of this intervention in everyday practice.
Number of discharges before noonDaily during the 3-month trial
Cost of care per patientFor entire 3 month study periodAverage cost of care per patients for each group for entire 3-month study period
Length of stayFor entire 3 month study periodAverage length of stay for each group for entire 3-month study period

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026