Improving Patient-reported Outcomes After Lung Cancer Surgery With Mobile Internet Platform
NCT ID: NCT06483295
Last Updated: 2025-05-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
216 participants
INTERVENTIONAL
2024-03-24
2026-12-31
Brief Summary
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Detailed Description
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This study aims to leverage mobile internet technology to transform traditional database construction, enhance the efficiency and accuracy of prospective database information collection, and establish a high-quality prospective database of postoperative lung cancer patient-reported outcomes. This will facilitate the analysis of factors influencing postoperative discomfort in patients and explore the role of interactive mobile internet technology platforms in improving postoperative PROs, thereby elevating the diagnostic and treatment standards in this field.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
NONE
Study Groups
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Group A
Mobile Internet Platform Follow-up Group
Using mobile internet platforms for follow-up management of postoperative symptoms in lung cancer patients.
Using mobile internet platforms for follow-up management of postoperative symptoms in lung cancer patients.
Group B
Traditional Outpatient Follow-up Group
No interventions assigned to this group
Interventions
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Using mobile internet platforms for follow-up management of postoperative symptoms in lung cancer patients.
Using mobile internet platforms for follow-up management of postoperative symptoms in lung cancer patients.
Eligibility Criteria
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Inclusion Criteria
2. Owns and uses a smartphone and can use WeChat.
3. Volunteer to participate in this study and sign an informed consent form.
Exclusion Criteria
2. 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.
3. 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.
4. At any stage after entering the study, the patient voluntarily requests to withdraw or discontinue treatment due to personal reasons.
18 Years
80 Years
ALL
No
Sponsors
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Shanghai Chest Hospital
OTHER
Responsible Party
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Xinghua Cheng
Director, Head of Oncology Surgery, Clinical Professor
Principal Investigators
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Xinghua Cheng, MD
Role: PRINCIPAL_INVESTIGATOR
Shanghai Chest Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Locations
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Zuodong Song
Shanghai, Shanghai Municipality, China
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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ShanghaiChestPRO
Identifier Type: -
Identifier Source: org_study_id
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