Pulmonary Rehabilitation in Improving Lung Function in Patients With Locally Advanced Non-Small Cell Lung Cancer Undergoing Chemoradiation
Primary Purpose
Cachexia, Fatigue, Pulmonary Complications
Status
Withdrawn
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
exercise intervention
pulmonary complications management/prevention
quality-of-life assessment
questionnaire administration
Sponsored by
About this trial
This is an interventional supportive care trial for Cachexia focused on measuring Pulmonary Rehabilitation, Non-Small Cell Lung Cancer, NSCLC
Eligibility Criteria
Inclusion Criteria:
- Patients who have been diagnosed with locally advanced unresectable NSCLC undergoing definite chemo-radiation with curative intent
- Patients must be able to sign informed consent
- Patients who qualify for pulmonary rehabilitation as part of the standard of care and are covered by medical insurance
- Patients must be able to ambulate a minimum of 100 feet prior to enrollment in pulmonary rehab
- Patients must be willing and able to travel to the pulmonary rehabilitation site at the Morehouse Medical Plaza
Exclusion Criteria:
- Tumor resection candidates
- If survival is deemed less than 6 months for any medical condition
- If they have angina or unstable coronary disease
- Congestive heart failure refractory to medical management
- Malignancy with bone instability
- Inmates
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Arm I (early intervention)
Arm II (late intervention)
Arm Description
Beginning within 2 weeks of starting chemoradiation, patients undergo an individualized rehabilitation program comprising aerobic exercise and strength training, including treadmill walking, stationary bicycle, NU-Step, upper body resistance training and breathing retraining, 3 times per week for 8 weeks (36 sessions).
Beginning 1 month after completion of chemoradiation, patients undergo an individualized exercise rehabilitation program as in Arm I.
Outcomes
Primary Outcome Measures
Percent improvement in the 6 minute walk from prior to post PR
Either a two-sided t-test or a Wilcoxon-rank sum test will be used to test the difference in the improvement of the 6 minute walk depending on the distribution. This test will be used to compare the difference in improvement between PR during chemo-radiation of NSCLC patients and PR 8 weeks post chemo-radiation. Linear regression will be used to estimate which clinical characteristics and patient demographics are associated with improvement in 6 minute walk. The study population will be described using means and standard deviations or medians and the interquartile range.
Secondary Outcome Measures
Percent improvement in the St. George Respiratory Questionnaire (SGRQ) score
Feasibility of the program, based on number of patients attending the sessions throughout the 8 weeks
Either Pearson's chi-square of Fisher's exact methods will be used to test if the feasibility differs across groups. Logistic regression will be used to estimate which clinical characteristics and patient demographics are associated with feasibility.
Full Information
NCT ID
NCT02017925
First Posted
December 17, 2013
Last Updated
April 12, 2017
Sponsor
Ohio State University Comprehensive Cancer Center
1. Study Identification
Unique Protocol Identification Number
NCT02017925
Brief Title
Pulmonary Rehabilitation in Improving Lung Function in Patients With Locally Advanced Non-Small Cell Lung Cancer Undergoing Chemoradiation
Official Title
Pulmonary Rehabilitation in Locally Advanced Non-Small Cell Lung Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
April 2017
Overall Recruitment Status
Withdrawn
Study Start Date
October 2013 (undefined)
Primary Completion Date
March 2017 (Anticipated)
Study Completion Date
March 2017 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Ohio State University Comprehensive Cancer Center
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This randomized clinical trial studies pulmonary rehabilitation in improving lung function in patients with locally advanced non-small cell lung cancer undergoing chemoradiation. Individualized exercise rehabilitation programs may reduce breathing problems and improve quality of life in patients with non-small cell lung cancer. It is not yet known whether pulmonary rehabilitation is more effective when started during or after cancer treatment.
Detailed Description
PRIMARY OBJECTIVES:
I. To determine feasibility of pulmonary rehabilitation (PR) in patients with locally advanced unresectable non-small cell lung cancer (NSCLC) undergoing definite chemotherapy and radiation therapy.
II. To measure exercise capacity and respiratory symptoms in lung cancer patients receiving chemotherapy and radiation before and after pulmonary rehabilitation.
III. To compare if there are any differences in symptom relief, exercise capacity, and cancer treatment tolerability between performing pulmonary rehabilitation during chemo-radiation versus after completion of lung cancer treatment.
OUTLINE: Patients are randomized to 1 of 2 arms.
ARM I: Beginning within 2 weeks of starting chemoradiation, patients undergo an individualized rehabilitation program comprising aerobic exercise and strength training, including treadmill walking, stationary bicycle, NU-Step, upper body resistance training and breathing retraining, 3 times per week for 8 weeks (36 sessions).
ARM II: Beginning 1 month after completion of chemoradiation, patients undergo an individualized exercise rehabilitation program as in Arm I.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cachexia, Fatigue, Pulmonary Complications, Radiation Toxicity, Recurrent Non-small Cell Lung Cancer, Stage IIIA Non-small Cell Lung Cancer, Stage IIIB Non-small Cell Lung Cancer, Stage IV Non-small Cell Lung Cancer
Keywords
Pulmonary Rehabilitation, Non-Small Cell Lung Cancer, NSCLC
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Arm I (early intervention)
Arm Type
Experimental
Arm Description
Beginning within 2 weeks of starting chemoradiation, patients undergo an individualized rehabilitation program comprising aerobic exercise and strength training, including treadmill walking, stationary bicycle, NU-Step, upper body resistance training and breathing retraining, 3 times per week for 8 weeks (36 sessions).
Arm Title
Arm II (late intervention)
Arm Type
Experimental
Arm Description
Beginning 1 month after completion of chemoradiation, patients undergo an individualized exercise rehabilitation program as in Arm I.
Intervention Type
Behavioral
Intervention Name(s)
exercise intervention
Intervention Description
Undergo pulmonary rehabilitation
Intervention Type
Procedure
Intervention Name(s)
pulmonary complications management/prevention
Intervention Description
Undergo pulmonary rehabilitation
Intervention Type
Procedure
Intervention Name(s)
quality-of-life assessment
Other Intervention Name(s)
quality of life assessment
Intervention Description
Ancillary studies
Intervention Type
Other
Intervention Name(s)
questionnaire administration
Intervention Description
Ancillary studies
Primary Outcome Measure Information:
Title
Percent improvement in the 6 minute walk from prior to post PR
Description
Either a two-sided t-test or a Wilcoxon-rank sum test will be used to test the difference in the improvement of the 6 minute walk depending on the distribution. This test will be used to compare the difference in improvement between PR during chemo-radiation of NSCLC patients and PR 8 weeks post chemo-radiation. Linear regression will be used to estimate which clinical characteristics and patient demographics are associated with improvement in 6 minute walk. The study population will be described using means and standard deviations or medians and the interquartile range.
Time Frame
Baseline to up to 8 weeks
Secondary Outcome Measure Information:
Title
Percent improvement in the St. George Respiratory Questionnaire (SGRQ) score
Time Frame
Baseline to up to 8 weeks
Title
Feasibility of the program, based on number of patients attending the sessions throughout the 8 weeks
Description
Either Pearson's chi-square of Fisher's exact methods will be used to test if the feasibility differs across groups. Logistic regression will be used to estimate which clinical characteristics and patient demographics are associated with feasibility.
Time Frame
Up to 8 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients who have been diagnosed with locally advanced unresectable NSCLC undergoing definite chemo-radiation with curative intent
Patients must be able to sign informed consent
Patients who qualify for pulmonary rehabilitation as part of the standard of care and are covered by medical insurance
Patients must be able to ambulate a minimum of 100 feet prior to enrollment in pulmonary rehab
Patients must be willing and able to travel to the pulmonary rehabilitation site at the Morehouse Medical Plaza
Exclusion Criteria:
Tumor resection candidates
If survival is deemed less than 6 months for any medical condition
If they have angina or unstable coronary disease
Congestive heart failure refractory to medical management
Malignancy with bone instability
Inmates
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Patrick Nana-Sinkam, MD
Organizational Affiliation
Ohio State University Comprehensive Cancer Center
Official's Role
Principal Investigator
12. IPD Sharing Statement
Links:
URL
http://cancer.osu.edu
Description
The Jamesline
Learn more about this trial
Pulmonary Rehabilitation in Improving Lung Function in Patients With Locally Advanced Non-Small Cell Lung Cancer Undergoing Chemoradiation
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