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
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
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