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Sleep Disorders Managed and Assessed Rapidly in Transient Ischemic Attack (TIA) and In Early Stroke

Does Acute Management of Sleep Disorders Improve Outcomes After Non-disabling Cerebrovascular Events?

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01528462
Acronym
SMARTIES
Enrollment
97
Registered
2012-02-08
Start date
2011-10-31
Completion date
2013-09-30
Last updated
2023-08-22

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

Conditions

Ischemic Attack, Transient, Restless Legs Syndrome, Sleep Apnea Syndromes, Sleep Disorders, Stroke

Keywords

Stroke, Ischemic Attack, Transient, Sleep Disorders, Sleep Apnea Syndromes, Restless Legs Syndrome, Chronobiology Disorders

Brief summary

The aim of the investigators was to determine whether the immediate management of any detected sleep disorders can improve outcomes in patients who have had a transient ischemic attack (TIA) or minor stroke. This group of patients is at high risk for having a recurrent stroke or TIA, and the investigators would like to investigate new ways of preventing potentially avoidable events. The treatment of sleep disorders immediately after a stroke or TIA may prove to be a novel method of avoiding future strokes and improving outcomes.

Detailed description

Every year, thousands of people in Canada either die or are permanently disabled after suffering a stroke. This costs our society billions of dollars in physician services, hospital expenses, and decreased productivity. Some individuals are slightly more lucky; instead of having a severe stroke, they have either a very mild stroke or temporary stroke symptoms, also known as a transient ischemic attack (TIA), and do not experience any loss of abilities. However, mild strokes and TIA's can precede the onset of a more serious, disabling stroke. Most of the significant strokes that happen after a mild stroke or TIA occur within days of the original event; there is a need for early interventions that could prevent such occurrences. One of the goals of recent research has been to find ways to prevent major strokes after individuals have sustained a minor stroke or TIA. Up until now, stroke doctors have focused on treating elevated blood pressures and cholesterol levels, scanning the blood vessels in the neck for significant narrowings, and searching for irregular heart rhythms, all of which are treatable conditions that put patients at risk for having a stroke. Despite research which shows that sleep disorders such as sleep apnea (abnormal pauses in breathing during sleep) or restless legs syndrome (which can cause involuntary leg movements in sleep) are possible risk factors for stroke, these conditions are not routinely investigated by stroke doctors after a TIA or stroke. The investigators hypothesize that the study patients, who will all receive an expedited sleep assessment and expedited treatment of their sleep disorders, will have at the 3-month follow-up assessment: (i) Significantly improved quality of life at 3 months compared to baseline measurements (primary outcome); (ii) Improved outcomes on measures of sleepiness, psychomotor vigilance, daily function, depressive symptoms, cognition, and blood pressure at 3 months (secondary outcomes).

Interventions

OTHERExpedited Treatment of Sleep Disorders

Patients in this arm will undergo an expedited polysomnogram (if clinically necessary) and early treatment of any sleep disorders. Sleep-related disorders will be managed with the currently recommended therapies; patients with obstructive sleep apnea will be treated with positional therapy, continuous positive airway pressure (CPAP), etc., and those with restless legs syndrome will be treated with standard treatments such as iron, or dopaminergic agonists. Patients will also be counselled on improving their sleep hygiene and adjusting the timing of their medication administration to optimize efficacy. Furthermore, patients will receive information handouts.

Sponsors

Canadian Institutes of Health Research (CIHR)
CollaboratorOTHER_GOV
Heart and Stroke Foundation of Canada
CollaboratorOTHER
Canadian Stroke Network
CollaboratorOTHER
Sunnybrook Research Institute
CollaboratorOTHER
Sunnybrook Health Sciences Centre
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

1. Inclusion Criteria: * Patients presenting within 14 days of symptoms with either * High risk TIA * Minor stroke. * High risk TIA will be defined as: * Transient, acute motor or speech disturbance lasting at least 5 minutes, or * Any TIA associated with \>50% ipsilateral carotid stenosis (presumed to be symptomatic) or atrial fibrillation not currently anticoagulated * Mild stroke will be defined as focal neurological deficits with MRI changes and a National Institutes of Health Stroke Scale score ≤ 5 2.

Exclusion criteria

* Past history of impulse control disorder, gambling, or active psychiatric disease * Patients with cognitive impairment restricting ability to perform activities of daily function and ability to comply with medical therapy (e.g. CPAP or medication use) * Patients with limb weakness not allowing them to utilize a CPAP device * Life expectancy less than 6 months

Design outcomes

Primary

MeasureTime frameDescription
Change in quality of lifeBaseline, 3 monthsQuality of life will be measured by the Stroke Specific Quality of Life Scale (Williams LS, Weinberger M, Harris LE, Clark DO, Biller J. Development of a stroke-specific quality of life scale. Stroke 1999;30(7):1362-9).

Secondary

MeasureTime frameDescription
Change in performance on Psychomotor vigilance taskBaseline, 3 monthsThe reference for this measure is: Lim J, Dinges DF. Sleep deprivation and vigilant attention. Ann N Y Acad Sci. 2008;1129:305-22.
Change in National Institutes of Health (NIH) Stroke Scale scoreBaseline, 3 monthsThis is a measure of stroke severity. The reference for this measure is: Brott T, Adams HP, Olinger CP, et al. Measurements of acute cerebral infarction: a clinical examination scale. Stroke 1989;July 20(7):864-70.
Change in Barthel IndexBaseline, 3 monthsThis scale is used to measure performance in basic activities of daily living. The reference for this measure is: Mahoney FI, Barthel D. Functional evaluation: the Barthel Index. Maryland State Medical Journal 1965;14:56-61.
Change in Modified Rankin ScaleBaseline, 3 monthsThis scale is used for measuring the degree of disability or dependence in the daily activities of people who have suffered a stroke. The reference for this measure is: Bonita R, Beaglehole R. Modification of Rankin Scale: Recovery of motor function after stroke. Stroke 1988;19(12):1497-1500.
Change in Epworth Sleepiness ScaleBaseline, 3 monthsThe reference for this scale is: Johns MW. A new method for measuring daytime sleepiness: the Epworth sleepiness scale. Sleep. 1991 Dec;14(6):540-5.
Change in Centre for Epidemiological Studies Depression ScaleBaseline, 3 monthsThe reference for this measure is: Parikh RM, Eden DT, Price TR, Robinson RG. The sensitivity and specificity of the center for epidemiologic studies depression scale in screening for post-stroke depression. Int J Psychiatry Med. 1988;18:169-181.
Change in serum HgbA1c and fasting lipid profileBaseline, 3 months
Change in blood pressureBaseline, 3 monthsBlood pressure will be measured via BpTru Device (www.bptru.com). This device measures the blood pressure 6 times during a single reading; its purpose is to eliminate or reduce the white coat effect by discarding the first measurement and averaging the remaining five.
Change in Montreal Cognitive Assessment (MoCA) scoreBaseline, 3 monthsThe reference for this measure is: http://www.mocatest.org/

Countries

Canada

Outcome results

None listed

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