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Effects of Head Elevation by a Bed on Sleep-disordered Breathing

M

Mackay Memorial Hospital

Status and phase

Unknown
Phase 1

Conditions

Sleep-disordered Breathing
Obstructive Sleep Apnea

Treatments

Procedure: Head elevation by an automatic adjustable bed

Study type

Interventional

Funder types

Other

Identifiers

NCT01785199
UWB-C-008

Details and patient eligibility

About

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.

Full description

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.

Enrollment

60 estimated patients

Sex

All

Ages

20 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Subjects known to have snoring or sleep-disordered breathing

Exclusion criteria

  • Refusal to participate
  • Pregnancy
  • Psychiatric disorders
  • Clinical instability in the previous month

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 4 patient groups, including a placebo group

normal (AHI < 5)
Placebo Comparator group
Description:
Patients who are eligible for this study will sleep on an automatic adjustable bed with a second PSG performed within the next one month.
Treatment:
Procedure: Head elevation by an automatic adjustable bed
mild OSA (AHI between 5 and 15)
Active Comparator group
Description:
Patients who are eligible for this study will sleep on an automatic adjustable bed with a second PSG performed within the next one month.
Treatment:
Procedure: Head elevation by an automatic adjustable bed
moderate OSA (AHI between 15 and 30)
Active Comparator group
Description:
Patients who are eligible for this study will sleep on an automatic adjustable bed with a second PSG performed within the next one month.
Treatment:
Procedure: Head elevation by an automatic adjustable bed
severe OSA (AHI > 30)
Active Comparator group
Description:
Patients who are eligible for this study will sleep on an automatic adjustable bed with a second PSG performed within the next one month.
Treatment:
Procedure: Head elevation by an automatic adjustable bed

Trial contacts and locations

1

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Central trial contact

Ching-Lung Liu, MD

Data sourced from clinicaltrials.gov

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