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The CLOQS Trial - Countdown Lights to Optimize Quality in Stroke

The CLOQS Trial - Countdown Lights to Optimize Quality in Stroke

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01148602
Acronym
CLOQS
Enrollment
3452
Registered
2010-06-22
Start date
2010-06-30
Completion date
2012-04-30
Last updated
2015-12-09

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

Conditions

Acute Stroke

Keywords

Acute stroke, Emergency departments, Quality Improvement, Improved Processes, tPA, door-to-needle, door-to-treatment

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.

Interventions

OTHERLED stopwatch-clock timers

We will attach a large, in-your-face red LED stopwatch-clock timers to the patient's stretcher at the moment of ED arrival to act as a constant visual reminder to all team members (physicians, RN's, CT technologists) of the urgency of the situation.

Sponsors

University Health Network, Toronto
CollaboratorOTHER
Unity Health Toronto
CollaboratorOTHER
Sunnybrook Health Sciences Centre
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Improved door-to-CT and door-to-needle times.18 monthsImproved door-to-CT scan times and door-to-needle treatment times with tPA, with potentially improved response to treatment and reduction in adverse events.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026