Skip to content

The effect of preoperative short-term lung rehabilitation exercise on postoperative outcomes of lung cancer patients under neoadjuvant therapy: a prospective randomized controlled study

The effect of preoperative short-term lung rehabilitation exercise on postoperative outcomes of lung cancer patients under neoadjuvant therapy: a prospective randomized controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091123
Enrollment
Unknown
Registered
2024-10-21
Start date
2024-11-01
Completion date
Unknown
Last updated
2024-10-28

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

Conditions

Lung Cancer

Interventions

Rehabilitation group:preoperative short-term pulmonary rehabilitation (PR)

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Diagnosed clinically or pathologically as stage IIa-IIIB lung cancer; (2) 18 <= Age <= 80 years old; (3) Patients scheduled for surgical treatment at West China Hospital of Sichuan University; (4) Patients who plan to undergo 2-3 cycles of neoadjuvant chemotherapy combined with immunotherapy before surgery; (5) There are no potential contraindications related to pulmonary rehabilitation, including those who have experienced myocardial infarction or cerebrovascular accidents within six months; Chronic heart failure, unstable angina, severe arrhythmia, severe left heart dysfunction, acute pulmonary embolism or pulmonary embolism, severe lower limb vasculitis or limb dysfunction, etc; (6) Those who agree to be included in the study and sign the informed consent form after being informed of their condition.

Exclusion criteria

Exclusion criteria: (1) Incompatible collaborators (mental disorders, consciousness disorders, intellectual disabilities, etc.); (2) Individuals who cannot tolerate pulmonary rehabilitation training; (3) Patients with contraindications for pulmonary rehabilitation (as above); (4) Other exercise related taboos, such as active hemoptysis, untreated pneumothorax, etc; (5) Pregnant or lactating subjects; (6) Those who are unwilling or unable to cooperate with research requirements.

Design outcomes

Primary

MeasureTime frame
Postoperative pulmonary complication rate;

Secondary

MeasureTime frame
Static lung function ;Assessment of cardiorespiratory related functions;Quality of life Assessment;

Countries

China

Contacts

Public ContactGuowei Che

West China Hospital of Sichuan University

cheguoweixw@126.com+86 189 8060 1890

Outcome results

None listed

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