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Construction and Validation of a Predictive Model for Postoperative Lung Rehabilitation Based on Patient-Reported Outcomes

Construction and Validation of a Prediction Model for Postoperative Lung Rehabilitation Based on Patient-Reported Outcomes

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400090366
Enrollment
Unknown
Registered
2024-09-29
Start date
2024-10-01
Completion date
Unknown
Last updated
2024-09-30

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

Conditions

Lung lesions, including both malignant (e.g., lung cancer) and benign lung tumors

Interventions

Gold Standard:In this study, it does not involve the diagnosis of a specific disease, but rather an observational study focusing on the preoperative assessment and postoperative recovery of patients w
Index test:This study is an observational study and does not involve specific diagnostic tests, methods, biomarkers, or equipment to be evaluated. The goal of this study is to assess postoperative rec

Sponsors

Department of Thoracic and Cardiovascular Surgery, Fourth Affiliated Hospital of China Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age =18 years. 2. Underwent unilateral thoracoscopic lung wedge resection, segmentectomy, or lobectomy, with the surgical plan confirmed by a multidisciplinary team. 3. No preoperative contraindications that would severely affect postoperative recovery. 4. Able to understand the purpose of the study and sign the informed consent form. 5. No severe psychological disorders, able to comprehend study-related requirements.

Exclusion criteria

Exclusion criteria: 1. Received preoperative or postoperative adjuvant therapy. 2. Underwent simultaneous bilateral lung surgery or had a history of lung surgery. 3. Unable to tolerate surgery, has surgical contraindications, or a history of severe mental illness, making it impossible to understand the study content. 4. Patients unable to undergo postoperative follow-up (e.g., living in remote areas).

Design outcomes

Primary

MeasureTime frame
European Cancer Research and Treatment Organization Quality of Life Questionnaire;Questionnaire on Quality of Life Related to Lung Surgery;

Countries

China

Contacts

Public ContactXueying Yang

Department of Thoracic and Cardiovascular Surgery, The Fourth Affiliated Hospital of China Medical University

yangxueying@cmu.edu.cn+86 189 0401 9778

Outcome results

None listed

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