Actively Recruiting
Cognitive Function in Obstructive Sleep Apnea
Led by Comenius University · Updated on 2026-01-23
30
Participants Needed
1
Research Sites
165 weeks
Total Duration
On this page
Sponsors
C
Comenius University
Lead Sponsor
U
University Hospital Bratislava
Collaborating Sponsor
AI-Summary
What this Trial Is About
Obstructive sleep apnea (OSA) is the most common sleep-related breathing disorder and has been increasingly recognized as a contributor to cognitive decline and a potential risk factor for neurodegeneration. Previous studies have identified several associated comorbidities, including vascular dysfunction, metabolic alterations, and neuroinflammatory changes. However, the impact and underlying interplay of these pathophysiological mechanisms remain poorly understood due to the lack of integrated, multidimensional assessment. This prospective, observational, longitudinal cohort study aims to investigate cognition and OSA-related physiological and pathophysiological processes in 100 adults newly diagnosed with OSA, who have no history of chronic diseases (except for overweight and obesity) and are not receiving chronic medication. A subgroup of patients with moderate to severe OSA indicated for positive airway pressure (PAP) therapy will be followed to evaluate its long-term effects on cognitive function and related mechanisms. All participants will undergo polysomnography (PSG), comprehensive neuropsychological assessment, brain MRI with volumetric analysis, biomarker profiling from blood and saliva, and evaluation of endothelial function, baroreflex sensitivity, and gut microbiome composition at baseline and after 12 months. PAP adherence will be continuously monitored. The primary objective of this study is to characterize the profile of cognitive impairment associated with OSA. Secondary exploratory analyses will focus on factors contributing to neurocognitive dysfunction in OSA.
CONDITIONS
Official Title
Cognitive Function in Obstructive Sleep Apnea
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Signed informed consent.
- Age between 18 and 65 years.
- Newly diagnosed obstructive sleep apnea confirmed by overnight polysomnography with apnea-hypopnea index (AHI) of 5 or more events per hour.
- Able to complete required tests and follow-up visits.
You will not qualify if you...
- History of any chronic disease except overweight and obesity.
- Severe psychiatric conditions affecting cognitive functions.
- Chronic use of medication or nicotine that may influence study results.
- Neuropsychological assessment conducted less than 6 months before study start.
- Prior treatment for obstructive sleep apnea (e.g., CPAP, surgery, oral appliance).
- Motor or sensory impairments that interfere with test completion.
- Not using Slovak as native language for daily communication.
- Deemed unsuitable for enrollment by clinical judgment.
AI-Screening
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Trial Site Locations
Total: 1 location
1
1st Department of Neurology, Faculty of Medicine, Comenius University and University Hospital Bratislava, Slovakia
Bratislava, Slovakia, 813 72
Actively Recruiting
Research Team
B
Branislav Kollar, prof. MD PhD. MPH.
CONTACT
S
Stela Biathova, MA
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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