ChiCTR2600118708已完成Unknown
Effectiveness of Inspiratory Muscle Training on Dyspnea and Fatigue among Critically-Ill Burn Patients Receiving High-Flow Nasal Oxygen Therapy: A Randomized Controlled Trial
Self-financed1 个研究点 分布在 1 个国家目标入组 56 人开始时间: 2025年11月10日最近更新:
试验速览
- 阶段
- Unknown
- 状态
- 已完成
- 发起方
- 入组人数
- 56
- 试验地点
- 1
- 主要终点
- Dyspnea
研究概览
简要总结
- To evaluate the effectiveness of inspiratory muscle training on dyspnea among critically ill burn patients receiving high-flow nasal oxygen therapy (pre-post test).
- To evaluate the effectiveness of inspiratory muscle training on fatigue among critically ill burn patients receiving high-flow nasal oxygen therapy (pre-post test).
- To find out the relationship between effectiveness inspiratory muscle training and patients’ sociodemographic data.
研究设计
- 研究类型
- Interventional
- 主要目的
- 随机平行对照
- 盲法
- None
入排标准
- 年龄范围
- 18 至 65（—）
- 性别
- All
入选标准
- •1.18–65 years old adults;
- •2.Second- or third-degree burn with >=20% TBSA;
- •3.Stable and cooperative;
- •4.Under high-flow nasal oxygen therapy (HFNC);
- •5.Maximum Inspiratory Pressure (MIP) Ranges between 9 and 41 cmH2O.
排除标准
- •1.Unstable chronic cardiovascular or respiratory diseases.
- •2.Present acute respiratory infections.
- •3.Mental or physical incapability for performing IMT.
- •4.Receipt of other therapies having an effect upon the study outcomes.
- •5.Maximum Inspiratory Pressure (MIP) Ranges under 9_ above 41 cmH₂O.
研究组 & 干预措施
Control group
Conventional care
Intervention group
Conventional care and inspiratory muscle training intervention (The inspiratory muscle training protocol used in the present study was designed and implemented in accordance with evidence-based respiratory rehabilitation guidelines, including the recommendations of the American Thoracic Society and the European Respiratory Society for respiratory muscle training, as well as contemporary clinical practice guidelines for the respiratory management of critically ill and burn patients receiving high-flow nasal oxygen therapy.)
结局指标
主要结局
Dyspnea
时间窗: one days and fourteen days after the intervention
Fatigue
时间窗: one days and fourteen days after the intervention
次要结局
未报告次要终点
研究者
研究点 (1)
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