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临床试验/NCT06201299
NCT06201299招募中不适用

Comparison of the Effectiveness of Chair-based and Standard Exercise Programs in People With COPD

Istanbul Medipol University Hospital1 个研究点 分布在 1 个国家目标入组 64 人开始时间: 2024年1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
招募中
发起方
入组人数
64
试验地点
1
主要终点
Exercise capacity assesment

研究概览

简要总结

Patients who are diagnosed with COPD by a pulmonology specialist and referred to pulmonary rehabilitation will be included in the study. Cases that meet the inclusion criteria will be randomized and divided into two groups, standard exercise program group (SGr) and chair-based exercise. program group will be called (ChGr). While standard exercises will be given to SGr, chair-based exercises will be applied to ChGr. All evaluation and initial training sessions of the cases will be held in the hospital. Apart from this, they will be asked to do their exercises at home with the exercise videos that will be sent to them. In order to ensure that home exercises are performed completely and correctly, 2 sessions of online simultaneous exercise training will be provided with a physiotherapist via videoconference on a smartphone, and exercise follow-ups will be carried out by calling once a week. The program duration is 8 weeks, 5 days a week.

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
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Being between the ages of 18-75 years
  • •Having a diagnosis of COPD diagnosed according to clinical diagnostic criteria according to the American Thoracic and European Respiratory Societies (ATS-ERS).
  • •Presence of dyspnea on exertion
  • •Stable clinical status at inclusion without infection or exacerbation in the previous 4 weeks *Having smart phone usage skills

排除标准

  • •Patients with severe comorbid diseases, unstable coronary artery disease, collagen vascular diseases and requiring high-flow oxygen therapy (˃ 3-4 L\min).
  • •A history of exertional syncope or the presence of any comorbidities (such as severe orthopedic or neurological deficits or unstable heart disease) that preclude exercise training.
  • •Having participated in a pulmonary rehabilitation program within the last 12 months.

研究组 & 干预措施

Chair-based Exercise Group

Experimental

Exercises will be performed with chair support.

干预措施: Chair-based Exercise Program (Other)

Standard Exercise Group

Experimental

Exercises will be performed using theraband.

干预措施: Standard Exercise Program (Other)

结局指标

主要结局

Exercise capacity assesment

时间窗: Change from baseline at 2 months

The 6-minute walking test will conduct in a 30-meter corridor in line with American Thoracic Society (ATS) guidelines. Participants will ask to walk as far as they can. Prior to and following the test, oxygen saturation, heart rate and Borg fatigue rating will measure, and the walking distance will record.

次要结局

  • Dyspnea evaluation(Change from baseline at 2 months)
  • Peripheral muscle strength measurement(Change from baseline at 2 months)
  • Pulmonary function tests (PFTs)(Change from baseline at 2 months)
  • Psychological status assessment(Change from baseline at 2 months)
  • Evaluation of fatigue(Change from baseline at 2 months)
  • Respiratory muscle strength measurement(Change from baseline at 2 months)
  • Evaluation of quality of life(Change from baseline at 2 months)
  • Physical activity level assesment(Change from baseline at 2 months)

研究者

发起方
Istanbul Medipol University Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

esra pehlivan

Assoc. Prof. Dr.

Istanbul Medipol University Hospital

研究点 (1)

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