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CPAP intervention for Obstructive Sleep Apnea

N/A
Waitlist Available
Led By Marie-Josée Brouillette, MD
Research Sponsored by McGill University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 months before the beginning of the intervention and up to 1 month after the end of the intervention.
Awards & highlights
No Placebo-Only Group

Summary

Obstructive sleep apnea (OSA) is a breathing disorder that is characterized by episodes of complete or partial cessation of respiration during sleep, associated with upper airway collapse, oxygen desaturation and sleep fragmentation. OSA is a condition frequently implicated in cognitive disturbances, as well as associated with health conditions such as hypertension, metabolic disturbances and heightened risk of heart disease, stroke and mortality. These conditions are also increased in persons living with HIV. Individuals suffering from OSA report an increase in daytime sleepiness, mood changes and decline in quality of life.OSA also portends economic and societal impact through lost productivity at work and motor vehicle accidents. The presence of OSA is therefore important to detect in those living with HIV as it is potentially treatable contributors to cognitive disturbances in HIV. Continuous Positive Airway Pressure (CPAP) is the recommended treatment of choice for OSA. CPAP has established efficacy in improving cognition (executive function, long-term verbal and visual memory, attention/vigilance and global cognitive functioning). Although CPAP has been associated with improvements in cognitive functioning in the general population, its effectiveness in improving cognition in HIV+ individuals has never been previously tested. Given that cognitive disturbances in this population are multi-factorial, determining whether treatment of OSA in this population improves cognition is key in improving the clinical management of HIV+ individuals, both for its negative impact on cognition, but also more generally for their health.

Eligible Conditions
  • HIV (Human Immunodeficiency Virus)
  • Obstructive Sleep Apnea
  • Cognitive Impairment

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 months before the beginning of the intervention and up to 1 month after the end of the intervention.
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 5 months before the beginning of the intervention and up to 1 month after the end of the intervention. for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Changes in Cognitive Performance measure (B-CAM)
Secondary study objectives
Adherence to the CPAP treatment
Changes Self-reported cognitive difficulties (C3Q)

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

3Treatment groups
Experimental Treatment
Active Control
Group I: CPAP interventionExperimental Treatment1 Intervention
Over the course of 4-7 months, participants will have to wear the CPAP every night, at least 4 hours per night.
Group II: Control 1Active Control1 Intervention
Eligible participants who declined to participate in the study. Their main study visit data will be used to compare with the intervention group.
Group III: Control 2Active Control1 Intervention
Eligible participants who were not approached, hence not given the opportunity to accept or decline. Their main study visit data will be used to compare with the intervention group.

Find a Location

Who is running the clinical trial?

McGill UniversityLead Sponsor
409 Previous Clinical Trials
1,018,430 Total Patients Enrolled
VitalAireIndustry Sponsor
4 Previous Clinical Trials
1,729 Total Patients Enrolled
ResMedIndustry Sponsor
136 Previous Clinical Trials
47,517 Total Patients Enrolled
~4 spots leftby Nov 2025