KCT0012275招募中不适用
A Multicenter, Prospective, Comparative, Randomized Clinical Trial to Compare and Evaluate the Efficacy and Safety of the Pulmonary Rehabilitation Software 'EB-S100' in Patients with Chronic obstructive pulmonary Disease, Against a Standard Treatment Control Group.
Emocog Co., Ltd.0 个研究点目标入组 64 人开始时间: 2025年11月7日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 64
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 主要目的
- Treatment
入排标准
- 年龄范围
- 19(Year) 至 No Limit(—)
- 性别
- All
入选标准
- •All of the following inclusion criteria must be met to participate in this clinical study.
- •Adults aged 19 years or older
- •Patients diagnosed with chronic obstructive pulmonary disease (COPD) according to the Korean clinical practice guidelines for COPD
- •FEV1/FVC ratio < 0.7 on pulmonary function testing
- •Patients diagnosed with COPD who require pulmonary rehabilitation exercise therapy
- •Able to read and write Korean without difficulty
- •Able to use mobile applications on general-purpose devices such as smartphones or tablet PCs without difficulty
- •Subjects who voluntarily agree to participate in this clinical study
排除标准
- •Subjects meeting any of the following exclusion criteria will not be eligible to participate in this clinical study.
- •Respiratory muscle dysfunction
- •Psychiatric disorders that prevent communication or compliance with instructions
- •Diseases or conditions that impair walking or make improvement in walking ability difficult, including cerebrovascular diseases, musculoskeletal disorders, or other severe malnutrition
- •Other diseases that may result in death or disability within one year, including severe cancer, coronary artery disease, heart failure, or diabetes mellitus with severe complications
- •Pregnant women
- •Subjects deemed unsuitable for study participation at the investigator’s discretion
研究者
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