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临床试验/NCT07020182
NCT07020182尚未招募不适用

Efficacy Of Inpatient Pulmonary Rehabilitation Program In Elderly Patients With Acute Exacerbation Of COPD

Al-Azhar University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年6月10日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
60
试验地点
1
主要终点
Exercise tolerance

研究概览

简要总结

The study aimed to identify the effect of early pulmonary rehabilitation in elderly patients with Acute exacerbation (AE) of COPD (AECOPD) in exercise tolerance, dyspnea, sleep quality, fatigue, and time to discharge from hospital.

详细描述

A prospective supervised RCT (Randomized Controlled Trial) will be done include elderly COPD patients assigned randomly into two groups; Group A performed Physical therapy program, and Group B is control group completed two daily sessions from day 1 of hospital admission till discharge from the hospital .The study duration will be 12 weeks

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

盲法说明

The codes were determined by using serially numbered block size will be kept in sealed and opaque envelopes in a locked office

入排标准

年龄范围
65 Years 至 78 Years(Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients with acute exacerbation of COPD in both gender
  • •Patient older than 65 years
  • •Patient with clear consciousness
  • •Patients had been diagnosed with shortness of breath or dyspnea that was not caused by heart disease, pneumothorax, or pulmonary edema

排除标准

  • •Patient with systolic blood pressure lower than 90 mmHg
  • •Patient with an unstable psychological status, hemoptysis, pneumothorax, pulmonary edema

研究组 & 干预措施

Group A will perform physical therapy program

Experimental

Study group In this study we will study the impact of exercise training include breathing exercise, low-load resistance exercise (15%-30% of 1 repetition maximum (1-RM) as tolerated), aerobic training in the form of walking exercise under supervision of physiotherapist.In patients exercise tolerance, dyspnea, fatigue, and time to discharge from hospital.

The study will be start from day 1 of hospital admission till discharge from the hospital.The study duration will be 12 weeks

干预措施: physical therapy program (Other)

Group B will the control group

No Intervention

control group

结局指标

主要结局

Exercise tolerance

时间窗: The study will be start from day 1 of hospital admission till discharge from the hospital.The study duration will be 12 weeks

The 6 minute walk test(6MWT)in meter to asses exercise tolerance

次要结局

  • Dyspnea(The study will be start from day 1 of hospital admission till discharge from the hospital.The study duration will be 12 weeks)
  • Length of hospital stay(LOS)(The study will be start from day 1 of hospital admission till discharge from the hospital.The study duration will be 12 weeks)
  • Fatigue level(The study will be start from day 1 of hospital admission till discharge from the hospital.The study duration will be 12 weeks)

研究者

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

Marwa Mohammed

Lecturer of physical therapy,Beni-suef University

Al-Azhar University

研究点 (1)

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