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Clinical Trials/NCT01796756
NCT01796756
Completed
Not Applicable

Quality Improvement in Handover of General Internal Medicine In-patients

University of British Columbia1 site in 1 country1,168 target enrollmentJanuary 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Quality Improvement in Patient Handoff
Sponsor
University of British Columbia
Enrollment
1168
Locations
1
Primary Endpoint
Proportion of patients handed over to the on-call resident/Clinical Associate (CA)
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

Miscommunication during patient handover can jeopardize patient safety and is the focus of Quality Improvement initiatives by many organizations. It is widely recognized that such miscommunication is preventable using a number of strategies identified in the literature.

Currently, there is no formal handover process of General Internal Medicine in-patients, otherwise known as the Clinical Teaching Unit (CTU) at Vancouver General Hospital, which is a major patient safety concern. This project will implement a formal handover program and evaluate whether there are changes in resident satisfaction with handover, but more importantly, whether the investigators can improve patient outcomes.

Registry
clinicaltrials.gov
Start Date
January 2013
End Date
November 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Residents, medical students, and patients
  • Residents and medical students will be any rotating through General Internal Medicine at Vancouver General Hospital
  • Patients will be any admitted to General Internal Medicine and cared for during on-call hours (defined as 18:00 - 07:00)

Exclusion Criteria

  • None for residents and medical students
  • Patients who are not being cared for during on-call hours (defined as 18:00 - 07:00)

Outcomes

Primary Outcomes

Proportion of patients handed over to the on-call resident/Clinical Associate (CA)

Time Frame: 5 months

Study Sites (1)

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