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NCT05365516 Clinical Trial

Medical Safety Huddles - a Multi-site QI Project

Patient Safety Clinical Trial

Official title:
Medical Safety Huddles - a Multi-site QI (Quality Improvement) Project

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05365516
Other study ID # 19-6357
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 1, 2020
Est. completion date January 30, 2023

Study information
Verified date May 2023
Source University Health Network, Toronto
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This quality improvement project will implement and evaluate the impact of physician-specific huddles, termed "medical safety huddles" on patient safety within four programs/sites at Sinai Health Systems, St. John's Rehab (Sunnybrook) and University Health Network.

Recruitment information / eligibility
Status Completed
Enrollment 4
Est. completion date January 30, 2023
Est. primary completion date October 31, 2022
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion criteria: - Any staff physicians, residents or medical students working at the four programs/sites Exclusion criteria: None

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Implementing medical safety huddles
These short, virtual huddles are led by a huddle leader and occur on a weekly or once every two week basis. Each site will be adapting the Medical Safety Huddles for their context and workflow to specifically engage physicians.

Locations
Country Name City State
Canada Bridgepoint Active Health Toronto Ontario
Canada Mount Sinai Hospital Toronto Ontario
Canada Princess Margaret Hospital - UHN Toronto Ontario1
Canada St John's Rehab Toronto Ontario

Sponsors (3)
Lead Sponsor Collaborator
University Health Network, Toronto Sinai Health System, Sunnybrook Health Sciences Centre

Country where clinical trial is conducted

Canada, 

Outcome
Type Measure Description Time frame Safety issue
Primary Adverse events We will examine whether the huddles impact the frequency and severity of adverse events experienced by patients. We will also determine if the huddles specifically impact certain types of adverse events in terms of frequency and severity. We will also perform analysis specific for each program/site. 19 months
Secondary Process measure - Attendance rate The number of physicians attending each huddle will be monitored to ensure the fidelity of implementation 15 months
Secondary Process measure - Safety issues The type and number of safety issues brought up during huddles will be monitored on a monthly basis to ensure the fidelity of implementation 15 months
Secondary Process measure - Actions taken to address safety issues The number of actions taken to address safety issues will be monitored on a monthly basis to ensure the fidelity of implementation 15 months
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