Lung cancer patients scheduled for surgical treatment
Conditions
Interventions
Prospectively collect data related to physical fitness such as resting heart rate, VO2max, physical activity and its intensity during the perioperative period of lung cancer using a wearable device.
Sponsors
Ohde Yasuhisa
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Patients have been registered in JCOG2217 prior to enrollment in this study. 2) Planned surgery for lung cancer has not yet begun. 3) Patients own a smartphone. 4) Written informed consent was obtained from the patient
Exclusion criteria
Exclusion criteria: 1) Those who have medical devices in their body that may be affected by magnetic materials, such as pacemakers or implanted defibrillators. 2) Those who have a history of hypersensitivity to silicone, rubber products, or metals. 3) Those who have a history of severe hypersensitivity. 4) Those who are otherwise deemed inappropriate by the attending physician.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Mean resting heart rate at 6 months after surgery (and the amount and percentage of change from pre-operative level) | — |
Secondary
| Measure | Time frame |
|---|---|
| Mean resting heart rate (and amount and percentage change from pre-operative levels) Mean VO2max (and amount and percentage change from preoperative levels) Percentage wearing wearable devices Mean period of MVPA Relationship between physical fitness-related indicators and patient treatment outcomes Relationship between surgery and postoperative changes in physical fitness-related indicators Relationship between postoperative changes in respiratory function and those in physical fitness-related indicators | — |
Contacts
Public ContactShinya Katsumata
Shizuoka Cancer Center
Outcome results
None listed