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临床试验/NCT06715228
NCT06715228招募中不适用

Efficacy of Shitali Respiratory Rehabilitation Program in Obstructive Sleep Apnea

Cairo University1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2024年11月7日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
40
试验地点
1
主要终点
apnea hypopnea index

研究概览

简要总结

obstructive sleep apnea has a negative impact on blood pressure of patients, sleeping quality, and respiration

详细描述

in this study, patients (n=40) with obstructive sleep apnea will participate in this study to be divided in to group I and group II with an equal number of patients (n = 20 for the group). Group I will administer six cycles of 5-min shitali respiratory pranayama exercise rehabilitation training (the rehabilitation will be repeated or applied at morning, afternoon, and also at evening) for 12 week as a daily performance, the other group, Group II, will act as control group.

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
35 Years 至 55 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •non-obese patients
  • •obstructive sleep apnea (mild and moderate form)

排除标准

  • •cardiac patients metabolic diseases kidney diseases

研究组 & 干预措施

group I

Experimental

in this group, patients (n=20) with obstructive sleep apnea will participate and will administer six cycles of 5-min shitali respiratory pranayama exercise rehabilitation training (the rehabilitation will be repeated or applied at morning, afternoon, and also at evening) for 12 week as a daily performance,

干预措施: shitali pranayama respiratory rehabilitation training (Behavioral)

Group II

No Intervention

in this group, patients (n=20) with obstructive sleep apnea will participate and will act as control group. In this group, no intervention will be applied

结局指标

主要结局

apnea hypopnea index

时间窗: it will be assessed after 12 weeks

it will be measured through a sleep study

次要结局

  • systolic blood pressure(it will be assessed after 12 weeks)
  • diastolic blood pressure(it will be assessed after 12 weeks)
  • Pittsburg sleep quality index(it will be assessed after 12 weeks)
  • respiratory rate(it will be assessed after 12 weeks)
  • Epworth sleepiness scale(it will be assessed after 12 weeks)
  • visual analogue scale of by-partner reported sleep difficulty(it will be measured after 12 weeks)

研究者

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

Ali Mohamed Ali ismail

Department of Physical Therapy for Cardiovascular/Respiratory Disorder and Geriatrics, Faculty of Physical Therapy

Cairo University

研究点 (1)

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