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The CLOQS Trial - Countdown Lights to Optimize Quality in Stroke

Not Applicable
Completed
Conditions
Acute Stroke
Interventions
Other: LED stopwatch-clock timers
Registration Number
NCT01148602
Lead Sponsor
Sunnybrook Health Sciences Centre
Brief Summary

To reduce door-to-needle times in acute stroke treatment. Using an organizational behaviour intervention (a large stopwatch), we will post a visual cue to remind all parties that "time is brain". We hypothesize that this simple visual cue will improve door-to-CT scan times and door-to-needle treatment times, and thus improve treatment response, and reduce adverse events.

Detailed Description

We will construct a large, "in-your-face" red LED stopwatch-clock that is the intervention. The clock will be attached to the stretcher of patients presenting for hyperacute stroke treatment (consideration of tissue plasminogen activator (tPA) treatment at the moment of their Emergency department arrival. This will act as a constant visual reminder to all team members (physicians, RN's, CT technologists) of the urgency of the situation. The study will be a block randomization, by week of presentation. All patients presenting during "on" weeks will have a stopwatch timer with them during the hyperacute stroke workup. During "off" weeks, the clocks will not be used.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
3452
Inclusion Criteria
  • All patients who present to the emergency room with acute stroke for consideration of treatment with tPA.
Exclusion Criteria
  • Patients presenting to the emergency room (door time) more than 4.5 hours after symptom onset

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
'On Clock"LED stopwatch-clock timersLED stopwatch-clock timers will be posted for all patients presenting during "ON clock" weeks. All patients presenting with hyperacute stroke will be managed normally with the addition of a visual stopwatch timer.
Primary Outcome Measures
NameTimeMethod
Improved door-to-CT and door-to-needle times.18 months

Improved door-to-CT scan times and door-to-needle treatment times with tPA, with potentially improved response to treatment and reduction in adverse events.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (3)

Sunnybrook Health Sciences Centre

🇨🇦

Toronto, Ontario, Canada

University Health Network - Toronto Western Hospital

🇨🇦

Toronto, Ontario, Canada

St. Michael's Hospital

🇨🇦

Toronto, Ontario, Canada

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