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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00221065
Other study ID # TRI REB 04-043
Secondary ID TRI REB 04-043
Status Completed
Phase Phase 3
First received September 13, 2005
Last updated February 4, 2009
Start date June 2005
Est. completion date October 2008

Study information

Verified date February 2009
Source Toronto Rehabilitation Institute
Contact n/a
Is FDA regulated No
Health authority Canada: Health Canada
Study type Interventional

Clinical Trial Summary

" Obstructive sleep apnea"(OSA) is a sleep breathing disorder. When a person with OSA tries to sleep the back of the throat closes and blocks the flow of air into lungs.When this happens, a person's sleep is disrupted, causing minor awakenings(which the individual may not recognize). This occurs many times throughout the night, causing poor sleep quality,excessive daytime sleepiness, poor concentration, and sometimes depression.It is possible that poor outcomes observed in stroke patients with OSA result from these neurocognitive phenomena, presumably by reducing effective participation in rehabilitation activities.OSA is treated with nasal continuous positive airway pressure(CPAP).CPAP therapy keeps the back of the throat open so that airflow is never blocked.The study is designed to investigate whether treatment of OSA with CPAP improves the results of rehabilitation.


Description:

Stroke occurs as a result of ischemic injury to neural tissue, as a result of cardiogenic or artery to artery embolism or intracranial arterial thrombosis. The traditional vascular risk factors, namely hypertension, diabetes mellitus, tobacco smoking, family history and hyperlipidemia as well as atrial fibrillation are major determinants of stroke risk. Obstructive sleep apnea (OSA) has been shown to be a risk factor for hypertension and,although the association is less strong, atherosclerotic heart disease.There is a high prevalence of OSA amongst stroke patients, on the order of 60 to 70%, which is tenfold higher than in the general healthy population. Recently, it has been shown that, in stroke patients undergoing inpatient rehabilitation,the presence of OSA predicts both a poor functional outcome and greater length of hospitalization in the rehabilitation unit, even after adjustment for stroke severity.

We propose to examine the effect of CPAP therapy on the neuropsychological and functional outcomes of stroke patients with OSA admitted to the Toronto Rehabilitation Institute Stroke Rehabilitation Unit in a prospective, randomized study. We hypothesize that, in stroke patients with OSA, CPAP therapy will improve indices of vigilance, attention, and cognitive performances well as motor function(as it does in OSA patients without stroke)when compared to those not treated with CPAP. Furthermore,we hypothesize that the outcome of rehabilitation, as assessed by neuropsychological and motor indices, will be improved in these patients.


Other known NCT identifiers
  • NCT00375479

Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date October 2008
Est. primary completion date October 2008
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- completed embolic, thrombo-embolic or hemorrhagic subacute strokes admitted within 3 weeks of stroke onset to the SRU of TRI.

- all subjects must be able to follow simple commands in English based upon the Speech Language therapist's intake assessment and have competency to provide informed consent to participate in the study.

Exclusion Criteria:

- brainstem strokes due to increased aspiration risk with CPAP.

- patients with previously diagnosed OSA or stroke.

- diseases primarily or frequently affecting the central nervous system, including dementia, Parkinson's disease, multiple sclerosis,Huntington's disease or Lupus.

- history of a psychotic disorder

- stroke secondary to traumatic brain injury.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Intervention

Device:
Nasal Continuous positive airway pressure - Tyco 420G
CPAP at determined pressure nightly for 1 month

Locations

Country Name City State
Canada Toronto Rehabilitation Institute Toronto Ontario

Sponsors (2)

Lead Sponsor Collaborator
Toronto Rehabilitation Institute The Physicians' Services Incorporated Foundation

Country where clinical trial is conducted

Canada, 

References & Publications (1)

Kaneko Y, Floras JS, Usui K, Plante J, Tkacova R, Kubo T, Ando S, Bradley TD. Cardiovascular effects of continuous positive airway pressure in patients with heart failure and obstructive sleep apnea. N Engl J Med. 2003 Mar 27;348(13):1233-41. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Neurological and functional scales 1 month No
Secondary Measurements of severity of obstructive sleep apnea and sleep structure 1 month No
Secondary Epworth Sleepiness Scale 1 month No
Secondary Stanford Sleepiness Scale 1 month No
Secondary Participation Assessment Scale 1 month No
Secondary Neuropsychological tests(other than primary outcomes) 1 month No
Secondary Neurophysiological tests (other than primary outcomes) 1 month No
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