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临床试验/NCT02507297
NCT02507297已完成不适用

Sleep-Disordered Breathing and PAP in Perinatal Depression

University of Michigan2 个研究点 分布在 1 个国家目标入组 29 人开始时间: 2016年1月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
29
试验地点
2
主要终点
Change in Hamilton Rating Scale for Depression (HRSD) Score, Minus the Sleep Item

研究概览

简要总结

The goal of this study is to understand the contribution of sleep-disordered breathing (SDB) to one of the most common and debilitating adverse pregnancy outcomes, perinatal depression. The study is a randomized trial to test the efficacy of positive airway pressure (PAP) on sleep and depression symptoms in perinatal women. Participants will be pregnant women with depression and sleep-disordered breathing. Participants will be randomly assigned to receive either PAP therapy (PAP group) or treatment as usual within obstetrics (TAU group). Mood and sleep assessments will be completed at baseline, after 1 week of enrollment, and monthly thereafter through 12 weeks postpartum. Cortisol will be measured using saliva collection at baseline and again 8 weeks later.

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
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • 20-32 weeks gestation with a single, live fetus
  • meet criteria for major depressive disorder per the Structured Clinical Interview for DSM-V (SCID)
  • respiratory distress index (RDI; includes apneas, hypopneas, and respiratory effort-related arousals)≥5 per ambulatory assessment plus apnea symptoms (snoring, witnessed apnea, daytime sleepiness, sleep disturbance, snort arousals)
  • stable dose (for ≥8 weeks) of a selective serotonin reuptake inhibitor (SSRI) OR free of all antidepressant medications past 4 weeks
  • obstetrics care is at the University of Michigan, and the woman plans on delivering her baby at the University of Michigan

排除标准

  • Diagnosis of bipolar disorder, posttraumatic stress disorder, schizophrenia or psychosis, dissociative disorders, eating disorder, obsessive-compulsive disorder, somatic symptom and related disorders, substance use disorder, panic disorder, agoraphobia per DSM-V
  • diagnosis of, or suspicion for, narcolepsy or REM behavior disorder
  • current SDB treatment; medical conditions for which PAP is contraindicated (e.g., pneumothorax, pneumocephalus, recent trauma, recent surgery)
  • evidence of risk for drowsy driving (excessive daytime sleepiness plus history of motor vehicle accident or near miss due to sleepiness, fatigue, or inattention in past 12 months).

结局指标

主要结局

Change in Hamilton Rating Scale for Depression (HRSD) Score, Minus the Sleep Item

时间窗: Baseline to 8 weeks after baseline, and at 12 weeks postpartum

Change in clinician-rated depression severity and symptoms, excluding the items which measure sleep. Total score range: 0-46. Higher scores represent more severe depression.

次要结局

  • Change in Epworth Sleepiness Scale (ESS) Score(Baseline to 8 weeks after baseline, and at 12 weeks postpartum)
  • Change in Salivary Cortisol(Baseline to 8 weeks after baseline)
  • Change in Edinburgh Postnatal Depression Scale Score(Baseline to 8 weeks after baseline, and at 12 weeks postpartum)
  • Change in Pittsburgh Sleep Quality Index Score(Baseline to 8 weeks after baseline, and at 12 weeks postpartum)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Leslie Swanson

Clinical Assistant Professor

University of Michigan

研究点 (2)

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