Development of Patient Tailored Guideline of Physical Activity for Lung Cancer

Not Applicable

• Conditions: Lung Cancer
• Interventions: Behavioral: comprehensive intervention

• Registration Number: NCT03215537
• Lead Sponsor: Samsung Medical Center

Brief Summary

This study aims to propose a perioperative comprehensive intervention based on health behavior model to improve cardiopulmonary function and quality of life among lung cancer patients following

Detailed Description

This study aims to propose a perioperative comprehensive intervention based on health behavior model to improve cardiopulmonary function and quality of life among lung cancer patients following:

1. understanding multi-dimensional factors affecting cardiopulmonary function and quality of life

2. development of multidisciplinary comprehensive intervention

3. evaluation the effects of comprehensive intervention using cluster design

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study Start: 2016-03-02
• Study First Submitted: 2017-07-05
• Study First Submitted QC: 2017-07-11
• Study First Posted: 2017-07-12
• Primary Completion: 2020-11-16
• Status Verified: 2021-02
• Last Update Submitted: 2021-03-16
• Last Update Posted: 2021-03-17
• Study Completion: 2023-12-02

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 176

Inclusion Criteria

• lung cancer patients before surgery

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Exclusion Criteria

• Eastern Cooperative Oncology Group Performance Status <1
• Neoadjuvant therapy
• Multiple cancer
• Recurrent lung cancer.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SEQUENTIAL

Arm && Interventions

Group	Intervention	Description
comprehensive intervention	comprehensive intervention	preoperative: exercise counseling postoperative : symptoms counseling and pulmonary rehabilitation

Primary Outcome Measures

Name	Time	Method
Changes of cardiopulmonary function	Baseline, 1 month after surgery, 6 months after surgery, 1year after surgery	six minute walk test

Secondary Outcome Measures

Name	Time	Method
Changes of pulmonary function	Baseline, 1 month after surgery, 6 months after surgery, 1year after surgery	forced expiratory volume at one second, forced vital capacity
Changes of physical activity	Baseline, 1 month after surgery, 6 months after surgery, 1year after surgery	wearable device
complication	1 month after surgery, 6 months after surgery, 1year after surgery	Pneumonia
Changes of quality of life	Baseline, 1 month after surgery, 6 months after surgery, 1year after surgery	quality of life questionnaire
Changes of Fatigue	Baseline, 1 month after surgery, 6 months after surgery, 1year after surgery	Fatigue questionnaire
Changes of physical fitness	Baseline, 1 month after surgery, 6 months after surgery, 1year after surgery	muscle strengths

Trial Locations

Locations (1)

Samsung Medical Center; 🇰🇷 Seoul, Korea, Republic of