Skip to content

Post-stroke Triage DOC: Simple Screening for Depression, Obstructive Sleep Apnea and Cognitive Impairment

Post-stroke Triage DOC: Simple Screening for Depression, Obstructive Sleep Apnea and Cognitive Impairment

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02007265
Enrollment
1504
Registered
2013-12-10
Start date
2012-04-30
Completion date
2014-04-30
Last updated
2015-11-25

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

Conditions

Cognitive Impairment, Depression, Obstructive Sleep Apnea, Stroke, Transient Ischemic Attack

Brief summary

The purpose of this study is to determine whether simple, evidence-based clinical screening be quickly and feasibly implemented (\>85% of patients in an average of \<6 minutes) in large-volume urgent transient ischemic attack (TIA)/stroke clinics to identify individuals at high risk for the three most common and devastating post-stroke co-morbidities (depression, obstructive sleep apnea and cognitive disorders).

Detailed description

We have created a simple screening tool (the DOC Screen) that will be routinely applied to all patients at a high-volume Regional Stroke Prevention Clinic. Consenting patients will also undergo gold standard research assessments in order to determine the diagnostic characteristics of the screen compared to gold standard research assessments.The proportion of eligible patients who complete DOC screening and the time for completion (mean, range, standard deviations) will be calculated from aggregated data for all new consults in the stroke prevention clinic. For patients who consented to undergo gold standard testing, sensitivity, specificity, positive predictive value, negative predictive value and likelihood ratios of the DOC screen will be calculated. Screening cut-points will be optimized using Receiver Operating Characteristic (ROC) and area under the curve analysis, and logistic regression will be applied to this ROC Curve analysis to control for variables such as age, sex, BMI and education. We hope to develop a pragmatic approach to screening the large, high-risk stroke prevention clinic population, allowing broad screening for these important health conditions. This could change routine standard of care across stroke prevention clinics and facilitate early identification and appropriate assessment of patients.

Interventions

None listed

Sponsors

Heart and Stroke Foundation of Ontario
CollaboratorOTHER
Sunnybrook Health Sciences Centre
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Attending outpatient TIA and Stroke Prevention Clinics at any of the three regional stroke centres.

Exclusion criteria

* Those who are unable to complete the screen complete the screen due to severe aphasia, severe motor dysfunction and those who are not fluent in English without translation available.

Design outcomes

Primary

MeasureTime frameDescription
Number of Participants with who completed the DOC Screen in 5 minutes or lessDay 1This outcome is defined as the number of DOC patients that took 5 minutes or less to complete the DOC Screening Form

Secondary

MeasureTime frameDescription
DOC Screen Diagnostic Characteristics compared to Gold Standard Research AssessmentsAverage 7 weeksTo determine the diagnostic characteristics of the mini-screens compared to gold standard research assessments and to determine whether when applied as one integrated test in a stroke clinic population they perform comparably to previously published studies.

Countries

Canada

Outcome results

None listed

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