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Construction and effect evaluation of APP-based structured education program of perioperative pulmonary rehabilitation for patients with high risk factors of adverse outcomes after lung cancer surgery

Construction and effect evaluation of APP-based structured education program of perioperative pulmonary rehabilitation for patients with high risk factors of adverse outcomes after lung cancer surgery

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200066698
Enrollment
Unknown
Registered
2022-12-14
Start date
2022-12-15
Completion date
Unknown
Last updated
2023-05-15

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:structured education pulmonary rehabilitation programme
Control group:Routine pulmonary rehabilitation

Sponsors

Affiliated Hospital of Zunyi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria: ? age = 18 years old; ? Patients who plan to undergo thoracotomy or thoracoscopic radical resection of lung cancer, whose condition is stable and can take care of themselves; ? Patients who meet the diagnostic criteria of lung cancer in the NCCN Guidelines and are pathologically diagnosed as lung cancer, with TNM stage ? ~ ?, and at least one of the following risk factors: Pulmonary diseases (COPD, tuberculosis, pulmonary interstitial fibrosis, etc.), asthma, low lung function, peak expiratory flow (PEF) 70 years old, smoking history, pathogenic airway colonization bacteria, body surface area (BSA) >1.68 ?, previous history of radiotherapy and chemotherapy, thoracic surgery history and trauma history; ? Normal thinking comprehension, language expression ability, can effectively communicate, have and can operate a smart phone; ? Volunteer to participate in this study.

Exclusion criteria

Exclusion criteria: Exclusion criteria: ? Patients with preoperative neurological dysfunction who can't autonomously operate; ? Those who need absolute bed rest due to other diseases; ? Communication disorders caused by various reasons; ? Patients who are severely weakened due to disease and cannot tolerate lung rehabilitation measures.

Design outcomes

Primary

MeasureTime frame
Postoperative pulmonary complications;

Secondary

MeasureTime frame
Lung function index;6 minutes walking test distance;Borg dyspnea score;LOS(length of stay);Tube drawing time;

Countries

China

Contacts

Public ContactChenShaolin

Affiliated Hospital of Zunyi Medical University

30363284@qq.com13762910513

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026