Principal Investigators

    Kaminska, Marta


    Research Institute of the McGill University Health Centre

    Contact information of lead PI



    Title of project or programme

    Cognition and Obstructive Sleep Apnea in Parkinson's Disease, Effect of Positive Airway Pressure Therapy (COPE-PAP Trial)

    Source of funding information


    Total sum awarded (Euro)

    € 300,385

    Start date of award


    Total duration of award in years



    Research Abstract

    Cognitive dysfunction (impaired memory, thinking, etc) frequently occurs in Parkinson’s disease (PD), often progresses to dementia, and profoundly affects quality of life. Obstructive sleep apnea (OSA) is a common disorder in the general population that is treatable with positive airway pressure (PAP) therapy. It is known to impair cognitive function, but whether treatment improves cognitive function is less clear. When already affected by a degenerative process like PD, the brain might be more vulnerable to the effects of OSA, and more responsive to OSA treatment. To date, OSA has not been recognized as a significant factor in PD. In preliminary work in PD patients, we have found an association between OSA and poor cognition, and cognitive improvement with PAP therapy. We now wish to more rigorously evaluate the effect of OSA treatment on cognitive function in PD in a randomized controlled trial. Our primary objective is to assess, in PD patients with OSA and cognitive deficit, the effect of CPAP therapy on global cognitive function. We will also assess other non-motor symptoms of PD, quality of life, and specific domains of neurocognitive function. PD patients will be recruited from the McGill Movement Disorders Clinic and other Quebec Parkinson Network Centres. Participants will need to have evidence of cognitive deficit and presence of OSA on screening diagnostic polysomnography (sleep study). Ninety subjects will be randomly assigned to PAP or nasal dilator strips. Detailed neuropsychological testing and other measurements (including quality of life) will be done at baseline, 3 months and 6 months. At the end of the study period, subjects will have polysomnography on their respective treatment to assess efficacy with respect to OSA treatment. This study may demonstrate that a non-pharmacologic intervention has the potential to have a marked beneficial impact on cognitive function and quality of life in a significant proportion of PD patients

    Further information available at:

Types: Investments < €500k
Member States: Canada
Diseases: N/A
Years: 2016
Database Categories: N/A
Database Tags: N/A

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