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Development and Application of a Postoperative Dyspnea Nursing Intervention Program for Non-Small Cell Lung Cancer Patients Based on Symptom Management Theory

Development and Application of a Postoperative Dyspnea Nursing Intervention Program for Non-Small Cell Lung Cancer Patients Based on Symptom Management Theory

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500107365
Enrollment
Unknown
Registered
2025-08-11
Start date
2025-08-11
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Lung Cancer

Interventions

Observational group:Standard Nursing Interventions for Dyspnea
Intervention group:Received the dyspnea nursing intervention based on Symptom Management Theory

Sponsors

The First Affiliated Hospital , Army Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) Pathologically confirmed diagnosis of non-small cell lung cancer (NSCLC); 2) Aged 18-80 years; 3) Underwent video-assisted thoracic surgery (VATS) for lung cancer with ASA physical status classification I-III; 4) Willing to participate and provided signed informed consent after full explanation of the study; 5) Presence of postoperative dyspnea (Borg score >=2) at rest or during sitting on postoperative day 1; 6) Preoperative FEV1% >=50% without severe cardiopulmonary comorbidities.

Exclusion criteria

Exclusion criteria: 1) Lung cancer recurrence or distant organ metastasis; 2) Patients converted from video-assisted thoracic surgery (VATS) to open thoracotomy; 3) Concurrent other malignancies requiring treatment, or severe comorbidities in major organ systems; 4) Under protective medical care (where full disclosure is medically contraindicated); 5) Patients receiving neoadjuvant therapy preoperatively or scheduled for postoperative radiotherapy/chemotherapy; 6) Current participation in other clinical trials; 7) Inability to cooperate (due to psychiatric disorders, cognitive impairment, intellectual disability, etc.); 8) Postoperative mechanical ventilation >48 hours or active bleeding.

Design outcomes

Primary

MeasureTime frame
Dyspnea score;

Secondary

MeasureTime frame
Cardiopulmonary function;Postoperative 30-day pulmonary complication rate;Postoperative symptoms;Quality of life after surgery;Postoperative psychological status ;

Countries

China

Contacts

Public ContactLei Liu

The First Affiliated Hospital , Army Medical University

ttcrystalma@163.com+86 130 3830 0661

Outcome results

None listed

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