The Construction and Validation of a Core Symptom Management Plan for Perioperative Lung Cancer Patients Based on Network Analysis Method

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2500105991

Enrollment

Unknown

Registered

2025-07-15

Start date

2024-03-10

Completion date

Unknown

Last updated

2025-07-21

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:Core Symptom Management Plan

control group:Ordinary Providence

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged over 18 years old; 2. The surgical method is thoracoscopic surgery; 3. Pathologically diagnosed as primary lung cancer; 4. Currently not receiving other treatments (radiotherapy, chemotherapy, biology, immunotherapy, etc.); 5. Informed consent and willingness to participate in the survey.

Exclusion criteria

Exclusion criteria: 1. Complicated with other malignant tumors, physical or psychological diseases; 2. Cognitive impairment, with speech communication or text comprehension disorders; 3. A history of previous pulmonary nodule resection; 4. Preoperative complicated with infectious diseases; 5. Implementation of protective medical care.

Design outcomes

Primary

Measure	Time frame
Chinese Version of M.D. Anderson Symptom Inventory;Brief Fatigue Inventory - Chinese Version;Cough Evaluation Test;Modified Medical Research Council Dyspnea Scale;	—

Secondary

Measure	Time frame
quality of life;Self-Efficacy for Managing Symptoms;	—

Countries

China

Contacts

Public ContactWang Huihong

Jiangnan University Affiliated Hospital

jndxwhh2024@163.com+86 159 5158 0577

Outcome results

None listed

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