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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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4 October 2021 |
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Main ID: |
NCT02363114 |
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Date of registration:
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09/02/2015 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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DOC Utility: Screening of Depression, Obstructive Sleep Apnea and Cognitive Impairment
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Scientific title:
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DOC Utility: Simple Screening of Depression, Obstructive Sleep Apnea and Cognitive Impairment to Identify Stroke Clinic Patients at Risk of Adverse Outcomes |
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Date of first enrolment:
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April 1, 2014 |
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Target sample size:
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6500 |
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Recruitment status: |
Active, not recruiting |
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URL:
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https://clinicaltrials.gov/show/NCT02363114 |
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Study type:
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Observational [Patient Registry] |
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Study design:
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Phase:
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Countries of recruitment
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Canada
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Contacts
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Name:
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Richard H Swartz, MD, PHD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Sunnybrook Health Sciences Centre |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Consecutive patients referred to regional stroke prevention clinics.
- This includes those discharged from hospital with a diagnosis of stroke or TIA, as
well as emergency department referrals.
- The DOC CRF will also be completed for patients who are unable to complete the screen
due to severe aphasia, severe motor dysfunction and language barriers (those who are
not fluent in English without translation available).
Exclusion Criteria:
- Patients whose reason for referral to the clinic is neither Stroke nor TIA, as well as
those who have been admitted to LTC/CCC facilities at the time of clinic visit.
Age minimum:
N/A
Age maximum:
N/A
Gender:
All
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Health Condition(s) or Problem(s) studied
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Obstructive Sleep Apnea
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Stroke
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Transient Ischemic Attack
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Cognitive Impairment
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Depression
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Primary Outcome(s)
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Number of Participants with any Adverse Event
[Time Frame: 1 Year from Initial Screen Date]
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Secondary Outcome(s)
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Number of Participants who have been admitted to a long-term care or complex continuing care facility
[Time Frame: 1 Year from Initial Screen Date]
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Number of Participants who died
[Time Frame: 1 Year from Initial Screen Date]
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Number of Participants with recurrent stroke
[Time Frame: 1 Year from Initial Screen Date]
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Incidence of DOC co-morbidities
[Time Frame: 1 Year from Initial Screen Date]
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Number of Participants with myocardial infarction
[Time Frame: 1 Year from Initial Screen Date]
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Secondary ID(s)
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1012404
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141-2014
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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