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Effects of pulmonary tele-rehabilitation on motor capacity and lung function after surgical lobectomy for lung cancer:a 3-month follow-up single-blind randomized controlled trial protocol

Effects of pulmonary tele-rehabilitation on motor capacity and lung function after surgical lobectomy for lung cancer:a 3-month follow-up single-blind randomized controlled trial protocol

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500110205
Enrollment
Unknown
Registered
2025-10-10
Start date
2025-10-10
Completion date
Unknown
Last updated
2025-10-13

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

Conditions

lung cancer

Interventions

Intervention group:Receive tele-rehabilitation programs via the mobile app
Control group:The patient and their family will receive a brochure containing training instructions and explanations. The patient is required to conduct 5 sessions of 45-minute training at home each w

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: All patients preparing to undergo surgical resection of lung cancer at West China Hospital of Sichuan University in Shangjinyuan District will be screened by a physiotherapist. The inclusion criteria are as follows: (1) Aged between 18 and 80; (2) Pulmonary lobectomy and segmental resection via VATS; (3) Clear postoperative pathological diagnosis of lung cancer; (4) No cognitive impairment, normal communication skills; (5) Sign informed consent

Exclusion criteria

Exclusion criteria: (1) Preoperative or postoperative radiotherapy and chemotherapy; (2) Intraoperative bleeding (greater than 1500ml); (3) Reoperation or total pneumonectomy; (4) There are complications before surgery or complications after surgery that affect sports performance (such as musculoskeletal or nerve injury, serious hypoxemia, myocardial infarction within 30 days, hypertensive crisis, hemoptysis, gastrointestinal bleeding within 14 days, etc.)

Design outcomes

Primary

MeasureTime frame
6 minutes walking test;

Secondary

MeasureTime frame
postoperative complications;Forced expiratory volume in one second, FEV1;Forced vital capacity, FVC;SF-12 ;

Countries

China

Contacts

Public ContactCheng Shuhai

West China Hospital of Sichuan University

shuhai-cheng@foxmail.com+86 184 8201 2973

Outcome results

None listed

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