About this trial
Obstructive Sleep Apnea Syndrome (OSAS) is a chronic disease characterized by intermittent hypoxia and sleep fragmentation resulting from recurrent upper airway obstructions. The physiological and neurocognitive changes caused by the disease can affect how individuals perceive and interpret bodily sensations. Although body awareness plays a significant role in the perception and management of symptoms, its relationship with clinical parameters in individuals with OSAS has not been sufficiently investigated. Therefore, the aim of our study is to examine the relationship between body awareness and respiratory function, disease severity, fatigue, shortness of breath, and sleep quality in OSAS patients.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Receiving a diagnosis of OSA after polysomnography,
Having an Apnea-Hypopnea Index ≥5 for OSA,
Volunteering to participate in the study.
Disqualifiers
Having severe orthopedic, neurological, or cardiac diseases,
Having a diagnosed lung disease,
Having a previous or current history of psychiatric or neurological disorders,
Not voluntarily participating in the study.
Trial population
Patients with obstructive sleep apnea syndrome
Trial design
Case-only
Cross-sectional
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Body awareness
The Body Awareness Questionnaire (BAQ) will be used to assess individuals' body awareness. The scale score ranges from 18 to 26, with higher scores indicating higher awareness.
Dyspnea
Dyspnea is assessed with the modified Medical Research Council (mMRC) dyspnea scale. As the score increases, shortness of breath increases.
Disease severity
The evaluation will be based on the Apnea/Hypopnea index measured by polysomnography. An Apnea-Hypopnea Index \>5 indicates Obstructive Sleep Apnea Syndrome.
Fatigue severity
Fatigue will be assessed using the Fatigue Severity Scale. A score of 36 or higher indicates severe fatigue.
Sponsors and contacts
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