Obstructive Sleep Apnea Clinical Trial
Official title:
Effects of Head Elevation by an Adjustable Bed on Sleep-disordered Breathing
Sleep is known to be a dynamic state of consciousness that is characterized by rapid fluctuations in autonomic activity as well as changes in body postures. Body postures during sleep influence the severity of sleep-disordered breathing because a supine position is associated with an increase in upper airway collapsibility and thus an increase in frequency and duration of snoring and apnea. Use of an adjustable bed to elevate patients' head might improve those conditions. The purpose of the present study is to determine whether use of an automatic adjustable bed is associated with reducing sleep-disordered breathing in patients with suspected obstructive sleep apnea (OSA) due to upper airway problems.
From the Chest and Otorhinolaryngology Department, patients with symptomatic
sleep-disordered breathing will be referred to the Sleep Center. After an interview these
subjects will undergo a full-night polysomnography (PSG). Patients who are eligible for this
study will sleep on an automatic adjustable bed with a second PSG performed within the next
one month. The automatic device is initiated when the patient suffers from apnea ≥ 10
seconds, which is detected by an ultra-wideband (UWB) sensor placed under the bed. The head
will be slightly elevated at an angle of 10 degrees lasting 10 seconds and then be put down
softly. Parameters of sleep efficiency and architecture, apnea-hypopnea index (AHI), and
oxygen saturation will be obtained during each PSG. According to the severity, enrolled
patients will be classified into 4 groups as normal (AHI < 5), mild OSA (AHI between 5 and
15), moderate OSA (AHI between 15 and 30) and severe OSA (AHI > 30).
Using an automatic adjustable bed will improve sleep-disordered breathing with a reduction
of AHI score is assumed. The minimal sample size is estimated to be 14 subjects per group
with the intention of providing 80% power and an overall two-sided 5% type I error. A total
of 60 subjects (15 subjects per group) will be enrolled to achieve the necessary number of
evaluable subjects, anticipating roughly a 10% drop-out rate.
Informed written consent will be obtained from all subjects. This study was approved by the
Mackay Memorial Hospital Institutional Review Board.
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Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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