Comprehensive Care Program for Their Return to Normal Life Among Lung Cancer Survivors

  • End date
    Feb 28, 2025
  • participants needed
  • sponsor
    Samsung Medical Center
Updated on 21 October 2021
lung cancer
lung carcinoma


The purpose of this study is to develop a comprehensive care program for their return to normal life and community among lung cancer survivors and evaluate the effectiveness of the program.


Lung cancer patients scheduled for curative surgery will be enrolled in this study. The comprehensive care program will be developed, and provided to the intervention group before and after surgery. Outcomes will be assessed 6 months and 1 year after surgery. To evaluate the effectiveness of the program, a control group will be enrolled first and used as a comparator.

Condition carcinoma lung, Bronchial Neoplasm, Pulmonary Disease, lung carcinoma, Lung Disease, Lung Neoplasm, lung tumor, Lung Cancer
Treatment Usual Care, Comprehensive Care Program
Clinical Study IdentifierNCT05078918
SponsorSamsung Medical Center
Last Modified on21 October 2021


Yes No Not Sure

Inclusion Criteria

Patients diagnosed with non-small cell lung cancer(NSCLC) and scheduled for curative resection
NSCLC with clinical stage -
Patients who understood the study and gave written informed consent

Exclusion Criteria

Recurred lung cancer
Patients with extra-pulmonary synchronous double primary cancer
Patients with history of other cancer diagnosis or treatment in the last 3 years
Drop Criteria
When surgery was canceled or pathologic stage IV was confirmed after surgery
Withdrawal informed consent
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer  to help accelerate the development of new treatments and to get notified about similar trials.

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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