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临床试验/NCT02080533
NCT02080533已完成1 期

Feasibility of Slow-paced Respiration Therapy for Treatment of a Symptom Cluster in Pulmonary Arterial Hypertension

University of Pennsylvania2 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2014年2月最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
10
试验地点
2
主要终点
Adherence to slow-paced respiration therapy.

研究概览

简要总结

Pulmonary arterial hypertension (PAH) is a chronic illness characterized by increased pulmonary pressures resulting in right heart failure and premature death. Common symptoms that impair quality of life and functioning are dyspnea, fatigue and sleep disturbance. This trio of symptoms is highly prevalent and forms a symptom cluster (2 or more symptoms that co-occur) in PAH. From a biological, proinflammatory cytokines are implicated in dyspnea, fatigue and sleep disturbance; there is activation of the sympathetic nervous system (SNS) and an inherent inflammatory process in PAH that contributes to the pathophysiology, but the link to this symptom cluster has not been investigated. One novel, treatment for symptom clusters is slow-paced respiration therapy using the FDA-approved device, RESPeRATE. The device contains headphones and a sensor that attaches to the chest to detect inhalation and exhalation. Musical tones synchronize with the respiratory cycle to slowly guide the user to decrease respirations. RESPeRATE moderates effects of the SNS; lowers blood pressure; improves functional capacity and ejection fraction; and significantly decreases pulmonary pressures in left heart failure. The investigators will enroll 10 women with PAH to use the RESPeRATE device to perform slow-paced respiration for 15 minutes per day for 8 weeks to determine the feasibility and effects on the SNS and inflammatory activity and the symptom cluster. The investigator's overall hypothesis is that, as compared to baseline, after eight weeks of therapy women with PAH who receive slow-based respiration therapy will have lower SNS activity and inflammatory levels, and improved dyspnea, fatigue and sleep disturbance.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
21 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Previous documentation of mean pulmonary artery pressure > 25 mm Hg with a pulmonary capillary wedge pressure (or left ventricular end-diastolic pressure) < 16 mm Hg and PVR > 3 WU at any time before study entry.
  • Women with WHO Group I PAH (idiopathic, heritable, or associated with connective tissue disease, congenital heart disease, anorexigens or HIV)
  • Targeted PAH therapy at stable dose for 3 months
  • Age >21 years
  • Ability to perform six minute walk testing without limitations in musculoskeletal function or coordination.
  • Informed consent

排除标准

  • Age < 21
  • Hypotension (blood pressure < 90/60 mmHg)
  • Pregnancy
  • Chronic Fatigue Syndrome (current or history of)
  • Known sleep disorder (obstructive sleep apnea, restless leg syndrome, narcolepsy, current or history of)
  • Hospitalized or acutely ill
  • Major Depression (current or history of)
  • Lung transplant recipient

结局指标

主要结局

Adherence to slow-paced respiration therapy.

时间窗: 10 weeks

Adherence rates will be assessed by the frequency of days used.

次要结局

  • Change in baseline and Week 10 dyspnea scores on the Multidimensional Dyspnea Profile(Baseline and 10 weeks)
  • Change in baseline and Week 10 fatigue scores on the Multidimensional Fatigue Inventory(Baseline and 10 weeks)
  • Change in baseline and Week 10 sleep scores on the Pittsburgh Sleep Quality Index(Baseline and 10 weeks)
  • Change in baseline and Week 10 norepinephrine levels(Baseline and 10 weeks)
  • Change in baseline and Week 10 interleukin-6 levels(Baseline and 10 weeks)
  • Change in baseline and Week 10 tumor necrosis factor-alpha levels(Baseline and 10 weeks)
  • Change in baseline and Week 10 six minute walk test(Baseline and 10 weeks)
  • Change in baseline and Week 10 right ventricular systolic pressure(Baseline and 10 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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