Effects of Comprehensive Postoperative Pulmonary Tele-Rehabilitation in Elderly Patients With Resectable Lung Cancer

  • End date
    Feb 28, 2024
  • participants needed
  • sponsor
    Pusan National University Hospital
Updated on 7 October 2022
lung carcinoma


The purpose of this study is to confirm the effectiveness of a mobile messenger-based home tele-rehabilitation protocol in patients who have undergone lung resection surgery.

By analyzing the difference from the existing postoperative pulmonary rehabilitation, the investigators would like to propose a new pulmonary tele-rehabilitation protocol.

Condition Telerehabilitation, Carcinoma, Non-Small-Cell Lung, Cardiopulmonary Exercise Test
Treatment Pulmonary tele-rehabilitation, Control (Education)
Clinical Study IdentifierNCT05435885
SponsorPusan National University Hospital
Last Modified on7 October 2022


Yes No Not Sure

Inclusion Criteria

A person who is suspected of lung cancer and is scheduled to undergo a thoracoscopic lung resection surgery
men and women the age ≥65 years
A person who understands the course of the clinical trial and signs the informed consent form

Exclusion Criteria

Patients whose activity is restricted due to other diseases (e.g. osteoarthritis, spinal disease, cerebral infarction, etc.)
Patients who cannot test bioimpedance analysis due to the insertion of artificial pacemakers and defibrillators
A person who has difficulty judging himself/herself due to dementia, etc
Those enrolled in other clinical trials
A person deemed inappropriate to participate in this clinical trial under the judgement of the investigator
A person who cannot use mobile messenger
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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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