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临床试验/NCT01031914
NCT01031914已完成不适用

Evaluation of an Algorithm to Detect Sleep and Wake in Continuous Positive Airway Pressure Users Using Paced Breathing

Philips Respironics1 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2009年10月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
36
试验地点
1
主要终点
Sleep/Wake Algorithm

研究概览

简要总结

The purpose of this engineering trial is to develop and validate an algorithm that will deliver Paced Breathing as a ramp feature to obstructive sleep apnea (OSA) subjects using Continuous Positive Airway Pressure (CPAP) therapy. In this trial the investigators will be evaluating the algorithm's ability to correctly distinguish between sleep and wake.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
盲法
None

入排标准

年龄范围
21 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Age 21-70
  • •Diagnosis of obstructive sleep apnea (OSA)
  • •Current adherent CPAP user (has been using CPAP nightly for at least 2 weeks).
  • •On CPAP pressures of 5-10cm.
  • •Subjects wishing to complete a day or evening appointment need to have significant daytime sleepiness (Epworth Sleepiness Scale score of 8 or above)
  • •Able and willing to provide written informed consent
  • •English speaking

排除标准

  • •Participation in another interventional research study within the last 30 days
  • •Major controlled or uncontrolled medical condition such as congestive heart failure, neuromuscular disease, renal failure etc.
  • •Inability to tolerate nasal CPAP mask due to problems breathing solely through their nose.
  • •Chronic respiratory failure or insufficiency with suspected or known neuromuscular disease, moderate or severe chronic obstructive pulmonary disease (COPD), or any condition with an elevation of arterial carbon dioxide levels while awake (PaCo2≥55mmHg)
  • •Severe oxygen desaturation on the polysomnography (PSG), i.e. Sa02 < 70% for 10% of the study.
  • •Surgery of the upper airway, nose, sinus or middle ear within the past 90 days
  • •Currently using supplemental oxygen
  • •Regular use of sleeping pills or stimulants (> 3 nights a week)
  • •Currently working night shift or rotating day/night shift
  • •Drowsy Driving or near miss accident in the past 6 months
  • •Inability to tolerate or track to Paced Breathing device during initial habituation session in lab
  • •Chronic insomnia, Restless legs syndrome, or severe periodic limb movement disorder (PLMD - PLMAI>20/hr).

研究组 & 干预措施

Paced Breathing Sleep/Wake detection

Experimental

All subjects enrolled will have oobstructive sleep apnea (OSA) and will be current Continuous Positive Airway Pressur (CPAP) users.

干预措施: Paced Breathing (Device)

结局指标

主要结局

Sleep/Wake Algorithm

时间窗: The performance of the algorithm will be evaluated in real time while the subject is wearing the device during the sleep study, an average of 08 hours.

We tested the ability of the Sleep/Wake algorithm to identify sleep an wake periods with precision, as compared to standard polysonography (PSG) measures, which was used as the gold standard, i.e. we tested the accuracy of the algorithm. Accuracy was defined as the proportion of true results (both true positives and true negatives)in the population and it was assesed using as 2 X 2 table, i.e. accuracy = number of true positives + number of true negatives/ number of true positives + false positives + false negatives +true negatives. where True positive = the algorithm tested correctly identified sleep, False positive = the algorithm tested incorrectly identified sleep, True negative = the algorithm tested correctly rejected awake periods, and False negative = the algorithm tested incorrectly rejected awake periods.

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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