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临床试验/NCT00089752
NCT00089752已完成不适用

Impact of CPAP on Functional Outcomes in Milder Obstructive Sleep Apnea (CATNAP)

University of Pennsylvania8 个研究点 分布在 2 个国家目标入组 281 人开始时间: 2003年9月最近更新:
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
281
试验地点
8
主要终点
Change in the Score of the Functional Outcomes of Sleep Questionnaire at Baseline and Week 8 Treatment

研究概览

简要总结

The purpose of this study is to determine whether functional status improves in individuals with milder obstructive sleep apnea (OSA) following continuous positive airway pressure (CPAP) treatment.

详细描述

BACKGROUND:

OSA is characterized as mild, moderate, or severe, according to the number of respiratory disturbances per hour of sleep (RDI), as defined by the American Academy of Sleep Medicine. CPAP is the primary treatment for sleep apnea. The column of pressure delivered to the upper airway by this device immediately eliminates the respiratory disturbances when it is applied. There is evidence from randomized controlled studies that CPAP also improves functional status, and the key manifestation of OSA, including excessive daytime sleepiness, in individuals with severe OSI (i.e., RDI greater than 30). However, there has been limited research exploring improvement in functional status in individuals with less severe OSA (i.e., those with mild OSA and RDI of 5-15 or moderate OSA and RDI of 16-30). The large placebo effect that has been reported in controlled studies of OSA-associated functional outcomes mandates the need for a placebo in studies evaluating the true impact of this treatment. Results from the three randomized controlled studies in milder OSA that have examined this issue have been equivocal, principally because of serious methodological limitations. It remains unclear whether CPAP treatment improves daily functioning in those with milder OSA (RDI 5-30). This is a critical issue as this level of disease severity represents the largest segment of OSA and comprises 15% of the U.S. population.

DESIGN NARRATIVE:

Using Granger's model of functional assessment, this study will examine whether functional status improves in participants with milder OSA following CPAP treatment. The study will employ a randomized, placebo-controlled, parallel study design, and will use a sham CPAP device as the placebo in participants with significant daytime sleepiness. The study will test the hypothesis that the change in functional status (measured by the Functional Outcomes of Sleep Questionnaire) after 8 weeks of treatment will be greater for participants treated with active CPAP compared to the placebo. Secondary aims of the study include examining whether CPAP also improves daytime sleepiness, and determining whether CPAP can reduce nocturnal blood pressure to lower the risk for stroke and hypertension linked to OSA.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 100 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Active Treatment

Active Comparator

Continuous Positive Airway Pressure Treatment

干预措施: Continuous Positive Airway Pressure (CPAP) Treatment (Device)

Sham/Placebo Treatment

Placebo Comparator

Ineffective sham continuous positive airway pressure device with leak in interface to <1.0 cm H2O and resistance in motor to simulate normal operating noise and no compensation for leak.

干预措施: Sham CPAP device - CPAP device with pressure delivered <1 cm H20 (Device)

结局指标

主要结局

Change in the Score of the Functional Outcomes of Sleep Questionnaire at Baseline and Week 8 Treatment

时间窗: 8 weeks

The primary endpoint is change after 8 weeks of treatment from baseline value (controlling for baseline value) in the 30-item Functional Outcomes of Sleep Questionnaire (FOSQ) that will be used to test the primary study hypothesis that patients with milder OSA (RDI 5-30) on active treatment will demonstrate greater mean change for the Total score from baseline to 8 weeks treatment. The FOSQ is designed to assess the impact of excessive sleepiness on functional status. The instrument has established content validity, test-retest reliability (r= 0.91), and internal consistency (alpha = 0.96). The scale ranges from 5 - 20 with normal functional status being a value greater than 17.

次要结局

  • Change in the Score From Baseline to 8 Weeks Treatment Epworth Sleepiness Scale(Measured at Baseline and Week 8 of treatment in ITT sample)
  • Change in Mean Arterial Daytime Pressure at Baseline and Week 8 Treatment(Measured at Baseline and Week 8 treatment in the ITT sample)
  • Change in the Score From Baseline to 8 Weeks Treatment Measured by the Profile of Mood States(Measured at Baseline and Week 8 treatment in the ITT sample)
  • Change in the Score From Baseline to 8 Weeks Treatment on the SF36 - Physical(Baseline and Week 8 of treatment in ITT sample.)
  • Change in the Number of Lapses From Baseline to 8 Weeks Treatment on the Psychomotor Vigilance Task (PVT) - Total Lapses in 20 Minute Test(Baseline and 8 weeks of treatment in the ITT sample)
  • Change in the Score From Baseline to 8 Weeks Treatment SF-36 Mental Component(Baseline and after 8 weeks of treatment in ITT sample)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (8)

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