Clinical Trials Directory

Trials / Completed

CompletedNCT00679809

Safety, Fatigue, and Continuity in the Intensive Care Unit (ICU)

Safety, Fatigue, and Continuity in the ICU: a Pragmatic Mixed-methods Study

Status
Completed
Phase
Study type
Observational
Enrollment
19 (actual)
Sponsor
The Hospital for Sick Children · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

The purpose of this study is to describe the features of continuity and quantify fatigue in three ICU resident work schedules, estimate the frequency of preventable adverse events, and inform the design and demonstrate the feasibility of a future multi-centre study.

Detailed description

The overall goal of our research is to describe the optimal scheduling pattern for frontline physicians working in ICUs. Our hypothesis is that call schedule associated reductions in fatigue are counterbalanced by reductions in continuity, resulting in no change in the safety of patients. This is a prospective before-after, two-centre study using a mixed-methods design. We will apply 3 work schedules, each for a period of 2 months over a 6 month period in the adult medical-surgical ICUs at two university affiliated hospitals in Toronto. In this mixed methods approach, quantitative and qualitative data will be collected concurrently, analysed separately, and their results compared, to produce an integrated interpretation of the impact of work schedule on the relationship between continuity and fatigue. This will evaluate healthcare continuity and fatigue, describe adverse events in ICUs, identify the two best resident schedules for subsequent comparison, and demonstrate the feasibility of a future multi-centre study of physician scheduling.

Conditions

Timeline

Start date
2008-10-01
Primary completion
2009-07-01
Completion
2013-12-01
First posted
2008-05-19
Last updated
2015-06-01

Locations

3 sites across 1 country: Canada

Source: ClinicalTrials.gov record NCT00679809. Inclusion in this directory is not an endorsement.