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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01796756
Other study ID # H11-03542
Secondary ID
Status Completed
Phase N/A
First received February 14, 2013
Last updated January 14, 2016
Start date January 2013
Est. completion date November 2015

Study information

Verified date January 2016
Source University of British Columbia
Contact n/a
Is FDA regulated No
Health authority Canada: Health Canada
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 1168
Est. completion date November 2015
Est. primary completion date November 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group N/A and older
Eligibility 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)

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Caregiver), Primary Purpose: Health Services Research


Related Conditions & MeSH terms

  • Quality Improvement in Patient Handoff

Intervention

Other:
Handover program


Locations

Country Name City State
Canada Vancouver General Hospital Vancouver British Columbia

Sponsors (2)

Lead Sponsor Collaborator
University of British Columbia Canadian Medical Protective Association

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Other Proportion of patients the resident on-call did not receive information on that would have been useful 5 months No
Other Frequency of patients transferred to the ICU 5 months No
Other Frequency of patients referred to the Critical Care Outreach Team 5 months No
Other Frequency of inappropriate code blue calls for patients with a "do not resuscitate" order 5 months No
Other Aggregate length of stay of patients admitted to the Clinical Teaching Unit 5 months No
Other Aggregate rate of death of patients admitted to the Clinical Teaching Unit 5 months No
Other Resource Utilization for patients assessed by the resident on-call overnight Resource utilization will be defined by the ordering of: radiological imaging, blood work, electrocardiogram, blood transfusions, IV fluid administration, and antibiotics. 5 months No
Primary Proportion of patients handed over to the on-call resident/Clinical Associate (CA) 5 months No