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

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00679809
Enrollment
19
Registered
2008-05-19
Start date
2008-10-31
Completion date
2013-12-31
Last updated
2015-06-01

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

Conditions

Fatigue

Keywords

Resident, Safety, Fatigue, Continuity, ICU

Brief 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.

Interventions

None listed

Sponsors

The Hospital for Sick Children
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* All residents at participating ICUs starting a rotation in Fall 2008 * Staff members supervising and/or working with participating residents * Patients/family members under the care of the participating residents * Patients admitted to participating ICUs

Exclusion criteria

* Lack of informed consent

Design outcomes

Primary

MeasureTime frame
Fatigue6 months
Continuity of patient care6 months

Secondary

MeasureTime frame
Adverse events6 months
Preventable adverse events6 months
Feasibility6 months

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 5, 2026