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Effects of Different Physical Therapy Programs on Pulmonary Rehabilitation in Patients With Lung Cancer

Not Applicable
Conditions
Rehabilitation
Registration Number
NCT04914624
Lead Sponsor
Sun Yat-sen University
Brief Summary

This study applies external diaphragm pacemaker and positive expiratory pressure therapy to patients who received thoracic surgeries, in order to explore the effects of different physical therapy programs on pulmonary rehabilitation in patients with lung cancer. As well as we hope that these physical training programs can effectively improve the lung function of patients, reduce postoperative pulmonary complications, hospitalization days, hospitalization expenses, etc.

Detailed Description

This study applies external diaphragm pacemaker and positive expiratory pressure therapy to patients who received thoracic surgeries, ninety patients may be enrolled in this study.

Some metrics are used to evaluate the pulmonary rehabilitation status in postoperative patients which include pulmonary function test, 6-Min Walking Test,Borg index, complications incidence, chest tube draining time, and diaphragm muscle mobility.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
90
Inclusion Criteria
  1. Patients who are diagnosed with non-small cell lung cancer with clear pathological cytology by fiberoptic bronchoscopy and CT, and plan to undergo lobectomy or segmentectomy under general anesthesia for tracheal intubation;
  2. Age 18-80 years old;
  3. Those who have stable vital signs and can participate in this research;
  4. Pulmonary function test FEV1/FVC>0.8.
  5. Volunteer to participate in this research and sign an informed consent form.
Exclusion Criteria
  1. Pneumonectomy patients;
  2. Wedge resection patients
  3. Patients with distant metastasis of cancer;
  4. Patients with other malignant tumors;
  5. Severe complications occurred during the operation, and respiratory function training and testing are not allowed before and after Evaluator;
  6. Patients with severe physical or mental illness who cannot cooperate with the test;
  7. Patients with pacemakers, active tuberculosis, and pneumothorax.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
The change from baseline Forced Expiratory Volume In One Second at one month after surgerybaseline (before the surgery), and one month after surgery

Evaluate the change of Forced Expiratory Volume In One Second before the surgery and one month after surgery by conducting Pulmonary Function Test on resectable NSCLC patients

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Sun Yat sen University cancer center

🇨🇳

Guangzhou, Guangdong, China

Sun Yat sen University cancer center
🇨🇳Guangzhou, Guangdong, China
Jiudi Zhong, Bachelor
Contact
+86 13610181300
zhongjd@sysucc.org.cn
Qinglin Wang, Bachelor
Contact
+86 13826293429
wangql@sysucc.org.cn

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