跳至主要内容
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2024年1月20日

概览

阶段
不适用
干预措施
未指定
疾病 / 适应症
COPD
发起方
Istanbul Medipol University Hospital
入组人数
64
试验地点
1
主要终点
Exercise capacity assesment
状态
招募中
最后更新
去年

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.

注册库
clinicaltrials.gov
开始日期
2024年1月20日
结束日期
2025年12月1日
最后更新
去年
研究类型
Interventional
研究设计
Parallel
性别
All

研究者

发起方
Istanbul Medipol University Hospital
责任方
Principal Investigator
主要研究者

esra pehlivan

Assoc. Prof. Dr.

Istanbul Medipol University Hospital

入排标准

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.

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)

研究点 (1)

Loading locations...

相似试验