Actively Recruiting

Age: 18Years - 65Years
All Genders
NCT07364318

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

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

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.
Not Eligible

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

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

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

Loading map...

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

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here