NCT06483295

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

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
216

participants targeted

Target at P50-P75 for not_applicable lung-cancer

Timeline
8mo left

Started Mar 2024

Typical duration for not_applicable lung-cancer

Geographic Reach
1 country

1 active site

Status
recruiting

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

Study Progress78%
Mar 2024Dec 2026

First Submitted

Initial submission to the registry

March 13, 2024

Completed
11 days until next milestone

Study Start

First participant enrolled

March 24, 2024

Completed
3 months until next milestone

First Posted

Study publicly available on registry

July 3, 2024

Completed
4 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 7, 2024

Completed
2.5 years until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2026

Expected
Last Updated

May 28, 2025

Status Verified

May 1, 2025

Enrollment Period

4 months

First QC Date

March 13, 2024

Last Update Submit

May 22, 2025

Conditions

Keywords

patient-reported outcomesInternet

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

EXPERIMENTAL

Mobile Internet Platform Follow-up Group

Other: Using mobile internet platforms for follow-up management of postoperative symptoms in lung cancer patients.

Group B

NO INTERVENTION

Traditional Outpatient Follow-up Group

Interventions

Using mobile internet platforms for follow-up management of postoperative symptoms in lung cancer patients.

Group A

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

RECRUITING

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.

MeSH Terms

Conditions

Lung Neoplasms

Condition Hierarchy (Ancestors)

Respiratory Tract NeoplasmsThoracic NeoplasmsNeoplasms by SiteNeoplasmsLung DiseasesRespiratory Tract Diseases

Study Officials

  • Xinghua Cheng, MD

    Shanghai Chest Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

    PRINCIPAL INVESTIGATOR

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

Locations