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Physician-Nurse Dyad Rounding: A Collaborative Approach to Improve Unit-Level Metrics

Physician-Nurse Dyad Rounding: A Collaborative Approach to Improve Unit-Level Metrics

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06336915
Enrollment
300
Registered
2024-03-29
Start date
2023-01-03
Completion date
2025-07-22
Last updated
2025-07-28

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

Conditions

Wellness, Psychological

Brief summary

The project will be implemented on one unit at a time until the co-rounding process has been implemented on each Medical-Surgical unit. This study will involve the geo-localized hospitalist on the designated unit and the nursing staff involved in clinical patient care

Detailed description

Patient experience top box scores as well as doctor and nurse domains will be evaluated retrospectively prior to project implementation and this evaluation will continue to be evaluated six months after IRB approval and project initiation. Baseline patient experience scores are routinely captured as a part of routine data collection practices via Press Ganey survey administration. LOS and discharge times are also routinely collected as a part of routine data collection practices. LOS and average discharge times will be reviewed on an ongoing basis after project implementation to monitor for improvements.

Interventions

BEHAVIORALPhysician-Nurse Dyad Rounding

Collaborative Approach to Improve Unit-Level Metrics

Sponsors

Methodist Health System
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* Patient Experience, LOS, and Discharge Times: Private hospitalist patients at MDMC * LOS: Patients with a LOS ≤20 days

Exclusion criteria

* Patient Experience: Patients other than private hospitalist patients excluded from this measure. * LOS: Patients with LOS \>20 days are considered an outlier and will be excluded from the study

Design outcomes

Primary

MeasureTime frameDescription
Difference in percentage of discharged patients before 1400 (Mon-Fri) after project implementation compared to before implementationup to 100 weeksDifference in percentage of discharged patients before 1400 (Mon-Fri) after project implementation compared to before implementation

Secondary

MeasureTime frameDescription
Difference in Top Box Patient Satisfaction Scores and Doctor Domainup to 100 weeksDifference in top box patient satisfaction scores and doctor domain for private hospitalist patients after project implementation compared to before implementation
Difference in LOS of private hospitalist patients after project implementation compared to before implementationup to 100 weeksDifference in LOS of private hospitalist patients after project implementation compared to before implementation
Difference in collaboration and build positive relationships scores after project implementation compared to before implementationup to 100 weeksDifference in collaboration and build positive relationships scores after project implementation compared to before implementation

Countries

United States

Outcome results

None listed

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