Lung Rehabilitation in Treating Patients With Chronic Obstructive Pulmonary Disease Who Are Undergoing Surgery for Lung Cancer



Status:Active, not recruiting
Conditions:Lung Cancer, Cancer, Chronic Obstructive Pulmonary Disease, Smoking Cessation, Hospital, Pulmonary, Tobacco Consumers
Therapuetic Areas:Oncology, Pulmonary / Respiratory Diseases, Other
Healthy:No
Age Range:40 - 120
Updated:4/21/2016
Start Date:August 2006

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A Randomized Trial of Pulmonary Rehabilitation in Patients With Moderate to Severe COPD Who Require Lung Resection for Lung Cancer

RATIONALE: Exercise may help improve lung function and lessen complications of surgery in
patients with chronic obstructive pulmonary disease who are undergoing surgery for lung
cancer. It is not yet known whether lung rehabilitation is more effective than standard
therapy in improving lung function in patients with chronic obstructive pulmonary disease
who are undergoing surgery for lung cancer.

PURPOSE: This randomized clinical trial is studying lung rehabilitation to see how well it
works compared to standard therapy in treating patients with chronic obstructive pulmonary
disease who are undergoing surgery for lung cancer.

OBJECTIVES:

Primary

- Compare the impact of preoperative pulmonary rehabilitation (including upper and lower
extremity resistance training) vs usual care in patients with lung cancer and moderate
to severe chronic obstructive pulmonary disease who require lung resection for lung
cancer.

- Compare the impact of this study intervention vs usual care on functional status after
surgery.

OUTLINE: This is a randomized, multicenter study. Patients are randomized to 1 of 2
intervention arms.

- Arm I: Patients undergo pulmonary rehabilitation (including daily upper and lower
extremity resistance training, education, and smoking cessation counseling) twice a day
for 5 days prior to surgical resection. Beginning 2-3days after surgery, patients
undergo pulmonary rehabilitation once a day until discharge from the hospital.

- Arm II: Patients receive usual care (education and smoking cessation counseling alone)
twice a day for 5 days prior to surgical resection. Following surgery, patients will
receive usual care once a day until discharge from the hospital.

Days of hospitalization, ICU admissions, postoperative complications (i.e., pneumonia,
mechanical ventilation > 48 hours, or atelectasis requiring bronchoscopy) and spirometry and
imaging studies will be evaluated after surgery.

After completion of study intervention, patients are followed at 4-6 weeks, at 12 weeks, and
at 6 months.

PROJECTED ACCRUAL: A total of 90 patients will be accrued for this study.

DISEASE CHARACTERISTICS:

- Diagnosis of lung cancer

- Scheduled to undergo any thoracotomy for lung cancer resection (including wedge) or
VATS lobectomy or pneumonectomy for lung resection

- Diagnosis of COPD, meeting the following criteria:

- FEV_1/FVC < 0.71

- Smoking history ≥ 10 pack/years

- Presence of moderate to severe lung disease, meeting 1 of the following:

- FEV_1 ≤ 60% predicted*

- FEV_1< 80% predicted AND significant shortness of breath defined by a score of 2
or higher in the Medical Research Council Dyspnea Score NOTE: *Patients with an
FEV1 < 60% predicted (most severe) and scheduled to undergo VATS segmentectomy
or wedge resection will also be included.

PATIENT CHARACTERISTICS:

- Able to physically utilize exercise equipment as part of rehabilitation program

- No poor motivation or likely not to participate fully in PR program

- No recent history (within the past 3 months) of a clinically-significant myocardial
infarction, unstable angina, serious cardiac arrhythmia, or other serious medical
condition which the attending physician performing the preoperative evaluation deems
incompatible with participation in the study

PRIOR CONCURRENT THERAPY:

- Not specified
We found this trial at
1
site
Rochester, Minnesota 55905
?
mi
from
Rochester, MN
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