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临床试验/CTRI/2024/07/071176
CTRI/2024/07/071176尚未招募2 期

Comparative Analysis of High-Frequency Chest Wall Oscillation (HFCWO) vs. Traditional Chest Physiotherapy (CPT) in the Management of COPD - NI

O0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方
O

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1.Confirmed COPD Diagnosis: Participants must have a confirmed diagnosis of COPD.
  • 2.Specific Age Range: 18 Years to 45 Years.
  • 3.Stable Disease State: Participants should be in a stable COPD state without recent exacerbations.
  • 4.Informed Consent: Ability to provide informed consent for voluntary participation.
  • 5.Adherence to Treatment Protocols: Willingness to comply with HFCWO and CPT treatment protocols.
  • 6.Ability to Use HFCWO Device or Receive CPT: Physical capability to use HFCWO or receive CPT.
  • 7.Stable Medication Regimen: On a stable COPD medication regimen with documented changes.
  • 8.Compliance with Study Visits: Commitment to attending scheduled visits and assessments.
  • 9.No Contraindications: Absence of contraindications to HFCWO or CPT.
  • 10.Language Proficiency: Proficient in the language(s) used for study communication and assessments.

排除标准

  • 1.Unstable Medical Conditions: Exclusion of individuals with acute medical conditions other than COPD.
  • 2.Severe Cognitive Impairment: Exclusion of those with severe cognitive impairment affecting decision-making.
  • 3.Recent Exacerbations: Exclusion of participants with recent COPD exacerbations.
  • 4.Severe Respiratory Distress: Exclusion of individuals in severe respiratory distress or requiring urgent medical intervention.
  • 5.Contraindications to HFCWO or CPT: Exclusion of participants with contraindications to HFCWO or CPT.
  • 6.Inability to Use HFCWO or Receive CPT: Exclusion of individuals physically unable to use HFCWO or receive CPT.
  • 7.Pregnancy: Exclusion of pregnant individuals for safety reasons.
  • 8.Non-compliance with Study Requirements: Exclusion of those unwilling or unable to comply with study protocols.

研究者

发起方
O

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