Cognition and Obstructive Sleep Apnea in Parkinson's Disease, Effect of Positive Airway Pressure Therapy

Not Applicable

Completed

• Conditions: Obstructive Sleep Apnea; Parkinson's Disease
• Interventions: Device: auto-adjusting positive airway pressure; Other: Nasal dilator strips

• Registration Number: NCT02209363
• Lead Sponsor: McGill University Health Centre/Research Institute of the McGill University Health Centre

Brief Summary

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, the investigators have found an association between OSA and poor cognition, and cognitive improvement with PAP therapy. The investigators now wish to more rigorously evaluate the effect of OSA treatment on cognitive function in PD in a randomized controlled trial. The investigators primary objective is to assess, in PD patients with OSA and cognitive deficit, the effect of OSA treatment on global cognitive function. The investigators 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.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2014-07-31
• Study First Submitted QC: 2014-08-01
• Study First Posted: 2014-08-05
• Study Start: 2015-04
• Primary Completion: 2022-06
• Study Completion: 2022-12
• Status Verified: 2024-03
• Last Update Submitted: 2024-03-12
• Last Update Posted: 2024-03-13

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 91

Inclusion Criteria

• Parkinson's disease as perMDS criteria
• Evidence of cognitive dysfunction (clinical impression of mild cognitive impairment and MOCA <=27)
• Presence of OSA (apnea-hypopnea index RDI ≥ 15/h) on screening diagnostic polysomnography (PSG)
• Stable regimen of anti-PD medication for 1 month prior
• Adequate knowledge of English or French for completion of study assessment.

Exclusion Criteria

• Oxygen saturation <75% for >10% of the diagnostic polysomnography as this should lead to active PAP treatment
• Other major neurological disorder
• Unstable cardiac disease, uncontrolled hypertension, or diabetes
• Active cancer or other disorder with an expected survival < 6 months
• Active treatment of OSA (prior diagnosis of OSA will constitute an exclusion criterion only if the patient is currently being treated for the OSA)
• Significant vision or hearing impairment that could affect performance on neurocognitive assessment tasks.
• Latex allergy.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Positive airway pressure (PAP)	auto-adjusting positive airway pressure	Auto-adjusting positive airway pressure
nasal dilator strips	Nasal dilator strips	Sham treatment

Primary Outcome Measures

Name	Time	Method
Change in global cognitive function	6 months	Montreal Cognitive Assessment (MoCA) - score range 0-30.

Secondary Outcome Measures

Name	Time	Method
Change in non-motor symptoms of Parkinson's disease	3 months and 6 months	MDS-UPDRS part 1
Change in quality of life	3 months and 6 months	PDQ-39
Change in specific domains of neurocognitive function	3 months and 6 months	Detailed neurocognitive assessment including attention and working memory, executive function, language, memory and visuospatial function.
Change in global cognitive function	3 months	Montreal Cognitive Assessment (MoCA)

Trial Locations

Locations (3)

McGill University Health Centre; 🇨🇦 Montreal, Quebec, Canada

Jewish General Hospital; 🇨🇦 Montreal, Quebec, Canada

Montreal Neurological Hospital and Institute; 🇨🇦 Montreal, Quebec, Canada