Fatigue Clinical Trial
Official title:
Safety, Fatigue, and Continuity in the ICU: a Pragmatic Mixed-methods Study
Verified date | May 2015 |
Source | The Hospital for Sick Children |
Contact | n/a |
Is FDA regulated | No |
Health authority | Canada: Ethics Review Committee |
Study type | Observational |
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.
Status | Completed |
Enrollment | 19 |
Est. completion date | December 2013 |
Est. primary completion date | July 2009 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | N/A and older |
Eligibility |
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 |
Observational Model: Cohort, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
Canada | Mount Sinai Hospital | Toronto | Ontario |
Canada | St Michael's Hospital | Toronto | Ontario |
Canada | The Hospital for Sick Children | Toronto | Ontario |
Lead Sponsor | Collaborator |
---|---|
The Hospital for Sick Children |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Fatigue | 6 months | No | |
Primary | Continuity of patient care | 6 months | No | |
Secondary | Adverse events | 6 months | No | |
Secondary | Preventable adverse events | 6 months | No | |
Secondary | Feasibility | 6 months | No |
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