跳至主要内容
临床试验/NCT01582958
NCT01582958已完成不适用

The Effect of Osteopathic Manipulative Treatment on Patients With Chronic Obstructive Pulmonary Disease:Correlating Pulmonary Function Tests With Biochemical Alterations

Michigan State University2 个研究点 分布在 1 个国家目标入组 45 人开始时间: 2013年4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
45
试验地点
2
主要终点
Change from baseline in spirometry at 6 weeks and 12 weeks

研究概览

简要总结

This project proposes to test the hypothesis that osteopathic manipulative treatment (OMT) given to patients with moderate to severe chronic obstructive pulmonary disease (COPD) enrolled in a 12-week pulmonary rehabilitation program (PRP) will result in improved respiratory pump function over and above that seen in sham and control groups. Specifically, we will study the effects of three OMT techniques: (a) thoracic inlet indirect myofascial release; (b) rib raising with continued stretch of the paraspinal muscle to the L2 level; and (c) cervical paraspinal muscle stretch with suboccipital muscle release. The key clinical readouts will include: spirometry, P100 (and index of diaphragm and inspiratory muscle efficiency), maximum inspiratory pressure (MIP) and maximum expiratory pressure (MEP), as well as laser evaluation of chest wall excursion. Supplementing these objective parameters will be several more subjective clinical outcome measures: exercise tolerance (6-minute walk test), dyspnea (shortness of breath questionnaire), and quality of life questionnaire. Finally, an attempt will be made to correlate biochemical alterations that may shed light on the biological mechanism underlying the OMT procedures.

详细描述

According to the above directions (provide a more extensice description, if desired), I am choosing to just submit the brief summary.

Thank you, Sherman Gorbis, DO

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 (Participant)

入排标准

年龄范围
49 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • postbronchodilator FEV1/FVC <0.7 and FEV1 <80% predicted [FEV1 =volume that has been exhaled at the end of the first second of forced expiration] and FVC volume of air that can be forcibly blown out after full inspiration]
  • history of smoking >20 pack-years
  • stable condition at inclusion with no infection or exacerbation for at least two months
  • optimal medical therapy for at least eight weeks with no change

排除标准

  • history of active pulmonary disease such as asthma
  • positive bronchodilator test
  • treatment with N-acetylcysteine
  • previous diagnosis of hypertension or current anti-hypertensive treatment
  • known unstable or moderate to severe heart disease (arrhythmia, ischemic heart disease, or cardiomyopathy)
  • previous diagnosis of chronic illness such as diabetes, renal failure, hypercholesterolemia, hepatic cirrhosis, cancer, rheumatoid arthritis or any other systemic inflammatory disease
  • neuromuscular or disabling cognitive problems
  • engagement in any exercise-training program during the past three months
  • substance abuse in the preceding six months

结局指标

主要结局

Change from baseline in spirometry at 6 weeks and 12 weeks

时间窗: baseline, 6 weeks, 12 weeks

amount (volume) and/or speed (flow) of air that can be inhaled and exhaled

Change from baseline in P100 at 6 weeks and 12 weeks

时间窗: baseline, 6 weeks, 12 weeks

an index of diaphragm and inspiratory muscle efficiency (endurance)

Change from baseline in MIP (maximum inspiratory pressure) and MEP (maximum expiratory pressure)at 6 weeks and 12 weeks.

时间窗: baseline, 6 weeks, 12 weeks

assessments of inspiratory and expiratory muscle function, respectively

Change from baseline in inspiratory capacity at 6 weeks and 12 weeks.

时间窗: baseline, 6 weeks, 12 weeks

representing an indirect evaluation of chest wall excursion

次要结局

  • Change from baseline in exercise tolerance at 6 weeks and 12 weeks.(baseline, 6 weeks, 12 weeks)
  • Change from baseline in dyspnea (shortness of breath) at 6 weeks and 12 weeks.(baseline, 6 weeks, 12 weeks)
  • Change from baseline in profiling of the plasma metabolome at 6 weeks and 12 weeks.(baseline, 6 weeks, 12 weeks)
  • Change from baseline in quality of life at 6 weeks and 12 weeks.(baseline, 6 weeks, 12 weeks)
  • Change from baseline in profiling of plasma proteins at 6weeks and 12 weeks.(baseline, 6 weeks, 12 weeks)

研究者

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

Sherman Gorbis, DO, FAAO

Principal Investigator

Michigan State University

研究点 (2)

Loading locations...

相似试验