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Effect of CPET screening and preoperative pulmonary rehabilitation training on early postoperative rehabilitation in patients undergoing lobectomy for lung cancer

Effect of CPET screening and preoperative pulmonary rehabilitation training on early postoperative rehabilitation in patients undergoing lobectomy for lung cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082160
Enrollment
Unknown
Registered
2024-03-22
Start date
2024-03-25
Completion date
Unknown
Last updated
2024-03-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lung cancer

Interventions

Experimental group:Preoperative health education and pulmonary rehabilitation + postoperative routine respiratory training
Control group:Preoperative health education + postoperative routine respiratory training

Sponsors

Shanghai Fourth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1) Age 65 years and above; 2) Patients whose lung cancer diagnoses are all in accordance with the Chinese Medical Association Lung Cancer Clinical Diagnosis and Treatment Guidelines (2018 Edition) and who are proposed to undergo thoracoscopic lobectomy; 3) Patients who are conscious, without cognitive, speech and motor dysfunction and contraindications to exercise; 4) Patients and their families who agreed to be enrolled and signed the clinical informed consent to participate in this study; 5) American Society of Anaesthesiologists ASA classification I-III;

Exclusion criteria

Exclusion criteria: 1) Patients with multiple metastases throughout the body; 2) Patients with proposed total lung or two or more lobectomies; 3) patients receiving adjuvant treatment such as radiotherapy or chemotherapy; 4) Patients with severe organic lesions or insufficiency of organs such as heart, brain and kidney; 5) Patients with severe physical behavioural limitations requiring bed rest; 6) Patients with communication problems such as severe hearing, vision or speech disorders; 7) Patients with mental disorders; 8) Patients who have participated in other relevant clinical studies within 3 months;

Design outcomes

Primary

MeasureTime frame
6-minute walk distance;

Secondary

MeasureTime frame
Visual Analogue Score;Functional assessment of cancer therapy-lung;Postoperative tube placement time;Post-operative length of stay;

Countries

China

Contacts

Public ContactJing Feng

Shanghai Fourth People's Hospital

892080755@qq.com+86 157 3564 1483

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026