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The Impact of Physical Activity on the Postoperative Symptoms, Complications, and Quality of Life Among Lung Cancer

The Impact of Physical Activity on the Postoperative Symptoms, Complications, and Quality of Life Among Lung Cancer Survivors: A Prospective Cohort Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03705546
Enrollment
1050
Registered
2018-10-15
Start date
2016-03-04
Completion date
2026-03-03
Last updated
2024-05-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lung Neoplasms

Brief summary

The purpose of this study is to examine the impact of physical activity on the postoperative symptoms, complication, and quality of life.

Detailed description

Non-small cell lung cancer (NSCLC) survivor is increasing as developing early diagnosis and perioperative management. Despite multidisciplinary treatment, Surgery is the primary treatment option for cure in NSCLC. The patients with lung cancer who underwent surgery have limitation of pulmonary function and high risk of co-morbidities. Perioperative physical activity has been shown to reduce symptoms and prevent complications, improve long term quality of life after surgery. But validated exercise regimen has not been established for lung cancer patients. Therefore, Evidence-based guideline focusing on lung cancer after surgery is needed.

Interventions

None listed

Sponsors

Samsung Medical Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients who are diagnosed with lung cancer * Patients who are able to walk with ECOG (Eastern Cooperative Oncology Group) performance status \< 1 * Patients who understand the purpose of this study and provide the written informed consent

Exclusion criteria

* Patients who have difficulty for walking * Patients with history of other cancer in the last 3 years * Patients with neoadjuvant chemotherapy and/or radiation therapy * Patients who are diagnosed with recurrent lung cancer or multiple cancer * Foreigner of patients from overseas who are not able regularly participate in this study

Design outcomes

Primary

MeasureTime frameDescription
The change of quality of life: (EORTC QLQ) core30 (C30)Before surgery (baseline), and 1, 6, 12, 24, 36, 48, and 60 months after surgeryThe change of quality of life is measured using the European Organization for Research Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ) core30 (C30). The scale for quality of life is transformed into a score from 0 to 100, derived by 4-point Likert scale. A higher score represents a higher level of quality of life.

Secondary

MeasureTime frameDescription
Postoperative pulmonary complicationsWithin 30 days after surgeryIncidence of pulmonary complications including air leak, atelectasis, pleural effusion, pneumonia, etc.
The change of symptomBefore surgery (baseline), and 1, 6, 12, 24, 36, 48, and 60 months after surgeryThe change of symptom is measured using the European Organization for Research Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ) lung cancer module 13 (LC13). The scale for symptom is transformed into a score from 0 to 100, derived by 4-point Likert scale. A higher score represents a higher level of symptom.

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 28, 2026