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临床试验/NCT05781867
NCT05781867已完成不适用

Effect of Selective Manual Therapy Techniques in Chronic Obstructive Pulmonary Disease

Cairo University1 个研究点 分布在 1 个国家目标入组 52 人开始时间: 2023年3月20日最近更新:
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
52
试验地点
1
主要终点
cranio-vertebral angle and kyphotic angle in degrees

研究概览

简要总结

Our study aiming for determining the combined effect of selective manual therapy techniques in chronic obstructive pulmonary disease patients

详细描述

I will apply selective manual therapy techniques in form of mobilization techniques ,myofascial release techniques combined with traditional treatment to determine thier effect in chronic obstructive pulmonary disease patients

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
None

入排标准

年龄范围
50 Years 至 60 Years(Adult)
性别
Male
接受健康志愿者
是

入选标准

  • •All patients must diagnosed mild to moderate chronic obstructive pulmonary disease
  • •All patients should have foreward head and kyphosis

排除标准

  • •History of osteoporosis.
  • •Acute exacerbation.
  • •Presence of active hemoptysis
  • •Presence of malignant disease

研究组 & 干预措施

control

Placebo Comparator

26patients will be included in this group and will receive conventional physiotherapy in form of pursed lip breathing, diaphragmatic breathing exercise and Active Range of Motion of both upper extremities

干预措施: Manual therapy and conventional physical therapy treatment (Other)

manual therapy

Experimental

26patients will be included in this group and will receive manual therapy (chest mobilization, diaphragmatic myofascial release, myofascial release for pectoralis minor and major, scaleni ) and conventional physiotherapy

干预措施: Manual therapy and conventional physical therapy treatment (Other)

结局指标

主要结局

cranio-vertebral angle and kyphotic angle in degrees

时间窗: pre-intervention

kinovea software will be used to assess in degrees

chest expansion

时间窗: pre-intervention and after 8 weeks of intervention

caliper will be used to assess chest expansion into centimeter

(the forced vital capacity (FVC), forced expiratory volume at first second (FEV1) and FEV1/FVC will be recorded. )

时间窗: pre-intervention

spirometry used to measure

functional capacity.

时间窗: pre-intervention

Six minute walk test will be used to assess functional capacity(meter/minutes)

dyspnea score

时间窗: pre-intervention

Modified Medical Research Council dyspnea scale (mMRC dyspnea scale) will be used to assess dyspnea

次要结局

未报告次要终点

研究者

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

Amira saad mohamed

M.SC physical theray

Cairo University

研究点 (1)

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