Trial Information
Pulmonary Rehabilitation Before Lung Cancer Resection
Inclusion Criteria:
- Patient is scheduled to undergo a surgery for non small cell lung cancer
- Moderate to severe COPD
- Current or ex smoker of ten or more years
Exclusion Criteria:
- Unable to perform exercise due to active cardiovascular, musculoskeletal or mental
problems Poorly motivated to attend the rehabilitation sessions or receive
randomization.
Type of Study:
Interventional
Study Design:
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care
Outcome Measure:
Measure of length of hospital stay post surgical resection of lung cancer in patients that underwent a resection for lung cancer.
Outcome Description:
The length of hospital stay will be compared between participants that under went 10 Mindful Rehabilitation Sessions with participants who received the usual care prior to a lung resection.
Outcome Time Frame:
baseline to release from hospital - approx 10 days
Safety Issue:
No
Principal Investigator
Roberto P Benzo, MD
Investigator Role:
Principal Investigator
Investigator Affiliation:
Mayo Clinic
Authority:
United States: Federal Government
Study ID:
11-005820
NCT ID:
NCT01682850
Start Date:
September 2012
Completion Date:
October 2016
Related Keywords:
- Lung Cancer
- COPD
- Chronic Obstructive Lung Disease
- Emphysema
- COPD
- Chronic Obstructive Lung Disease
- lung cancer
- emphysema
- Pulmonary Rehabilitation
- Emphysema
- Pulmonary Emphysema
- Lung Diseases
- Pulmonary Disease, Chronic Obstructive
- Lung Neoplasms
- Lung Diseases, Obstructive
Name | Location |
Mayo Clinic |
Rochester, Minnesota 55905 |