Oral Appliance Therapy for Improving Sleep Quality During Pregnancy: A Controlled Clinical Trial
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 20
- 试验地点
- 2
- 主要终点
- Ratio of stable to unstable sleep from CPC
研究概览
简要总结
Many pregnant women suffer from poor sleep quality and snoring. Evidence shows an increasing association between (1) sleep disordered breathing and (2) maternal cardiovascular disease and in-hospital death. Snoring is a variant of obstructive sleep apnea (OSA) and OSA during pregnancy is associated with higher risks for cesarean delivery, gestational hypertension, preeclampsia and preterm delivery. It may also impact fetal outcomes negatively. The purpose of this study is to determine whether sleep quality can be improved in pregnant women who snore by means of an oral appliance that opens the airway. Sleep quality is evaluated objectively using an un-intrusive home sleep test system.
详细描述
As many as 20 percent of women suffer from snoring and poor sleep quality while pregnant. The purpose of this study is to determine whether sleep can be improved in pregnant women who snore by means of a midline traction oral appliance (OA) that opens the airway. This is an interventional study to objectively evaluate OA therapy on breathing during sleep as well as its effect on sleep quality. Pregnant women from all trimesters will be recruited. Each subject is expected to participate in the study for at least five (5) consecutive weeks. Home sleep recordings will be collected at three time points: T0 - Baseline prior to OA use for two consecutive nights; T1- first two consecutive nights wearing the OA; T2 - for two consecutive nights after 4 weeks of appliance use. In addition to the sleep studies performed at each of these time points, subjects will also complete several brief surveys. All participants will be given the opportunity to use their OAs after the 4 week period, and have their sleep recorded at 8 week intervals through the remainder of their pregnancies. Participants will get to keep and use their OAs after the study.
Pregnant women who snore (or otherwise have poor sleep), may qualify to participate in this study. Those who do not want to wear an oral appliance, but are interested in learning about sleep quality while pregnant, may also qualify to participate as a control subject.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Single (Outcomes Assessor)
盲法说明
Outcomes assessor reading the sleep studies will have the treatment arm masked.
入排标准
- 年龄范围
- 18 Years 至 45 Years(Adult)
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Pregnant adults who snore
- •At least 8 teeth per arch
- •Mallampati score from I to II
- •Palatine tonsils grade 0,1 or 2
- •Capable of giving verbal and written informed consent
- •Able to apply the sleep recorder and the oral appliance.
排除标准
- •Pregnant > 32 weeks
- •Uncontrolled serious health issues
- •Cardiovascular or cardiac rhythm disorders
- •Pharmacological dependency
- •Concomitant use of hypnotic agents or other sleep aids, nicotine or alcohol
- •Ongoing temporomandibular joint disorders
- •Loose teeth or periodontal disease
- •History of uvulopalatopharyngoplasty (UPPP)
结局指标
主要结局
Ratio of stable to unstable sleep from CPC
时间窗: Two nights of sleep recordings at each of 3 time point over 5 weeks.
Ratio of stable to unstable sleep based on cardiopulmonary coupling analysis.
次要结局
- Insomnia Sleep Questionnaire (ISQ)(At baseline and after 5 weeks)
- Pittsburgh Sleep Quality Index (PSQI)(At baseline and after 5 weeks)
- Hamilton Depression Rating Scale (HDRS)(At baseline and after 5 weeks)
- Number of snores per hour of sleep(At each of 3 time points over 5 weeks)
- Fatigue Severity Scale (FSS)(At baseline and after 5 weeks)
研究者
Emet D. Schneiderman, PhD
Professor, Biomedical Sciences
Texas A&M University
