Pulmonary Rehabilitation Before Lung Cancer Resection

Lung Cancer Clinical Trial

Official title:

Pulmonary Rehabilitation Before Lung Cancer Resection

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01682850
• Other study ID #: 11-005820
• Secondary ID: 1R01CA163293-01
• Status: Completed
• Phase: N/A
• Start date: August 2013
• Est. completion date: March 2019

Study information

• Verified date: January 2020
• Source: Mayo Clinic
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study seeks to study the effectiveness of a short mindfulness based pulmonary rehabilitation program prior to a surgical resection in patients with lung cancer and severe Chronic Obstructive Lung Disease (COPD).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 27
• Est. completion date: March 2019
• Est. primary completion date: December 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 40 Years to 100 Years

Eligibility

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.

Related Conditions & MeSH terms

• Chronic Obstructive Lung Disease
• COPD
• Emphysema
• Lung Cancer
• Lung Diseases
• Lung Diseases, Obstructive
• Lung Neoplasms
• Pulmonary Disease, Chronic Obstructive
• Pulmonary Emphysema

Intervention

Behavioral:
• Mindfulness Based Pulmonary Rehabilitation
Participants in this group will under go 10 sessions of mindfulness based pulmonary rehabilitation prior to surgery. Each session is about 2 hours long and consists of upper /lower extremity training, breathing exercises, and education.

Other:
• Usual Care

Locations

Country	Name	City	State
United States	University of Virginia	Charlottesville	Virginia
United States	Mayo Clinic	Jacksonville	Florida
United States	University of Pittsburgh	Pittsburgh	Pennsylvania
United States	Mayo Clinic	Rochester	Minnesota
United States	Washington University	Saint Louis	Missouri

Sponsors (2)

Lead Sponsor	Collaborator
Mayo Clinic	National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Measure of length of hospital stay post surgical resection of lung cancer in patients that underwent a resection for lung cancer.	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.	baseline to release from hospital - approx 10 days
Secondary	Measure post-operative complications in patients that under went 10 session of Mindful Pulmonary Rehabilitation prior to lung resection compared to patients who received usual care prior to a lung resection for lung cancer.	The study will compare the number of ICU days, ventilation hours, number of days with a chest tube, subsequent pneumonia or respiratory failure in patients that underwent 10 Mindful Pulmonary Rehabilitation sessions prior to a lung resection to patients who received the usual care prior to a lung resection for lung cancer.	Post surgerybaseline to release from hospital - approx 10 days

External Links

•   Mayo Clinic Clinical Trials