跳至主要内容
临床试验/KCT0012275
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

发起方
Emocog Co., Ltd.

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