Improving Patient-reported Outcomes After Lung Cancer Surgery With Mobile Internet Platform
Randomized Controlled Study on Improving Patient-reported Outcomes After Lung Cancer Surgery With Mobile Internet Platform
1 other identifier
interventional
216
1 country
1
Brief Summary
This study focuses on the significant impact of lung cancer in China, highlighted by its high incidence and mortality rates, influenced by factors like aging populations, smoking, and environmental issues. It emphasizes the importance of understanding the duration, severity, and factors affecting post-surgery symptoms like pain and coughing in patients. The research underlines the value of patient-reported outcomes (PROs) in enhancing postoperative care and survival rates through improved symptom monitoring and patient engagement. Utilizing internet technology, specifically a platform integrated with WeChat, the study aims to improve patient management and follow-ups post-discharge. The objective is to use mobile internet technology to build a high-quality prospective database on postoperative lung cancer patient outcomes, analyzing factors affecting postoperative discomfort and assessing the role of interactive platforms in improving patient care.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable lung-cancer
Started Mar 2024
Typical duration for not_applicable lung-cancer
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 13, 2024
CompletedStudy Start
First participant enrolled
March 24, 2024
CompletedFirst Posted
Study publicly available on registry
July 3, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 7, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2026
ExpectedMay 28, 2025
May 1, 2025
4 months
March 13, 2024
May 22, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
complaints of discomfort
MDASI-LC score for complaints of discomfort at postoperative months 1, 3 and 4 Postoperative discomfort chief complaint MDASI-LC score: Choose a number from 0 (asymptomatic) to 10 (the most severe level imaginable) for each item to indicate the severity of the symptoms. The main complaints of postoperative discomfort include: pain, cough, shortness of breath (key points) Other factors include fatigue, nausea, insomnia, depression, memory loss, loss of appetite, drowsiness, dry mouth, sadness, vomiting, numbness or stinging wounds, constipation, etc
4 months
Secondary Outcomes (4)
Life quality
4 months
Pulmonary function-the absolute value of FEV1
4 months
Pulmonary function-the percentage of FEV1 to expected values
4 months
Change of breath sounds
4 months
Study Arms (2)
Group A
EXPERIMENTALMobile Internet Platform Follow-up Group
Group B
NO INTERVENTIONTraditional Outpatient Follow-up Group
Interventions
Using mobile internet platforms for follow-up management of postoperative symptoms in lung cancer patients.
Eligibility Criteria
You may qualify if:
- Diagnosed with Stage I-III lung cancer and surgically resected at our centre.
- Owns and uses a smartphone and can use WeChat.
- Volunteer to participate in this study and sign an informed consent form.
You may not qualify if:
- Received any non-surgical anti-tumour therapy (radiotherapy, chemotherapy, targeted therapy or immunotherapy) for lung cancer during the follow-up period.
- After enrolment, preoperative emergence of serious comorbidities (inability to tolerate surgery or anaesthesia) that are not suitable for, or cannot be implemented as planned, in the study's treatment regimen.
- After admission, the patient's condition changes and the need to change from elective surgery to emergency surgery is confirmed by the doctor in charge.
- At any stage after entering the study, the patient voluntarily requests to withdraw or discontinue treatment due to personal reasons.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Zuodong Song
Shanghai, Shanghai Municipality, 200030, China
Related Publications (1)
Luo Y, Cheng Y, Song Z, Chen H, Bo Y, Shixing H. Patient-reported outcomes with a personalized follow-up program after lung cancer resection: A single-center randomized controlled trial. Asia Pac J Oncol Nurs. 2026 Jan 2;13:100844. doi: 10.1016/j.apjon.2025.100844. eCollection 2026 Dec.
PMID: 41625083DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Xinghua Cheng, MD
Shanghai Chest Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Director, Head of Oncology Surgery, Clinical Professor
Study Record Dates
First Submitted
March 13, 2024
First Posted
July 3, 2024
Study Start
March 24, 2024
Primary Completion
July 7, 2024
Study Completion (Estimated)
December 31, 2026
Last Updated
May 28, 2025
Record last verified: 2025-05