Patients and Intervention Patients

Patients and Intervention Patients eligible for the study were initially assessed via anamnesis, physical examination, and evaluation of inspi- ratory muscle strength. Subsequently, these patients were randomly allocated to phase II of the CRP into two groups: a group subjected to CRP+IMT (GCR+IMT) followed the IMT protocol in addition to the combined training (aerobic and resistance training) and a group subjected to CRP (GCR) followed the combined training protocol and performed breathing exercises for 12 weeks. An RMS test was conduct- ed before and after the intervention, and the functional capac- ity and QoL were evaluated. All evaluations were conducted by investigators blinded to the allocation of patients into the intervention groups.

結果 (繁體中文) 1:

Patients and Intervention
Patients eligible for the study were initially assessed via
anamnesis, physical examination, and evaluation of inspi-
ratory muscle strength. Subsequently, these patients were
randomly allocated to phase II of the CRP into two groups:
a group subjected to CRP+IMT (GCR+IMT) followed the
IMT protocol in addition to the combined training (aerobic
and resistance training) and a group subjected to CRP (GCR)
followed the combined training protocol and performed
breathing exercises for 12 weeks. An RMS test was conduct-
ed before and after the intervention, and the functional capac-
ity and QoL were evaluated. All evaluations were conducted
由不知道患者分配到調查
干預組。

結果 (繁體中文) 2:

患者與干預
符合研究條件的患者最初通過
麻醉、體格檢查和評估
肌肉力量。隨後，這些患者
隨機分配給 CRP 的第二階段分為兩組：
受 CRP_IMT （GCR_IMT） 影響的群體遵循
IMT協定，除了聯合訓練（有氧
和阻力訓練）和接受 CRP （GCR） 的組
遵循聯合訓練協定並執行
呼吸練習12周。RMS 測試是
干預前後，以及功能上限
對度和 QoL 進行了評估。進行了所有評價
由調查人員盲目地分配患者到
干預組。

結果 (繁體中文) 3:

病人與干預
符合研究條件的患者最初通過
inspi的記憶、體檢及評估-
肌肉力量。後來，這些病人
將CRP第二階段隨機分為兩組：
一組接受CRP+IMT（GCR+IMT）治療
除聯合訓練（有氧運動）外的IMT方案
和抵抗力訓練）和一組接受CRP（GCR）的患者
遵循聯合訓練方案
呼吸練習12周。進行了有效值測試-
干預前後ed及功能性capac-
評估ity和生活質量。所有評估都進行了
被調查者盲目地將病人分配到
干預組。