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
1268 participants
OBSERVATIONAL
2022-05-22
2030-08-20
Brief Summary
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Detailed Description
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It is helpful to relieve the patients and their families of the bad psychology, reduce the symptoms of patients, improve the patient's compliance behavior, relieve the psychological anxiety of patients, make it actively cooperate with the treatment, reduce complications, improve the quality of life of patients, so as to prolong the life cycle.
Our project is going to explore whether management and follow-up of locally advanced/metastatic patients using the patient process management platform can prolong patient survival and improve patient quality of life.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Platform follow-up cohort
This cohort will be managed and follow-up by patients' whole process follow-up platform. The patients can report the symptoms, get the reminder of the hospital visit, get the reminder of medicine taking, get the information of patients education.
Patients' whole process follow-up and management platform
Patients' whole process follow-up and management platform is a software for the patients and investigators. This platform will use to collect patients' information when they are out of patients and will provide the patients' education materials.
Routine follow-up cohort
This cohort will be managed and follow-up by the investigators or nurses. This cohort will take the routine follow-up and management way by the hospital.
No interventions assigned to this group
Interventions
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Patients' whole process follow-up and management platform
Patients' whole process follow-up and management platform is a software for the patients and investigators. This platform will use to collect patients' information when they are out of patients and will provide the patients' education materials.
Eligibility Criteria
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Inclusion Criteria
2. Male or female subjects who are over 18 years old (inclusive) at the time of signing the informed consent form.
3. The subject is diagnosed pathologically or cytologically with non-small cell lung cancer(NSCLC).
4. According to the 8th edition of the American Joint Committee on Cancer \[AJCC\], it is classified as stage IIB, stage III, stage IV NSCLC.
5. Not suitable for radical treatment or refuse surgery.
6. The life expectancy is not less than 3 months.
7. Be able to use a smartphone.
Exclusion Criteria
2. Presence of any other malignant tumor.
3. Patients who are expected to undergo radical surgery.
4. Currently participating in clinical trials.
5. Subjects who judged by the investigator to be unsuitable to participate in the trial.
18 Years
ALL
No
Sponsors
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Qianfoshan Hospital
OTHER
Responsible Party
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Jiandong Zhang
Director of Oncology Radiotherapy Department
Principal Investigators
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Jiandong ZHANG
Role: PRINCIPAL_INVESTIGATOR
Shandong First Medical University
Locations
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The First Affiliated Hospital of Shandong First Medical University
Jinan, Shandong, China
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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WYKA001
Identifier Type: -
Identifier Source: org_study_id
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