CompletedNot applicableNCT01068210

Lung Cancer Exercise Training Study

The purpose of the study is look at the effects of different types of exercise training with a stretching group and its effect on lung cancer patients. Subjects will take part in a 16 week training intervention that can consist of aerobic, resistance, aerobic \& resistance, or a control group. Pre and Post testing will include stress tests, echos, blood, and urine samples.

Checked against the public recordLast updated May 4, 2025 · Source: ClinicalTrials.gov

StatusCompleted
PhaseNot applicable
U.S. locations1
SponsorMemorial Sloan Kettering Cancer Center
01
Study overview

What this study is about

Purpose
Treatment
Study type
Interventional
Phase
Not applicable
Sponsor
Memorial Sloan Kettering Cancer Center
Interventions being studied
Behavioral: Aerobic Training; Behavioral: Progressive Stretching; Behavioral: Resistance Training; Behavioral: Aerobic and Resistance Training
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

03
Public criteria

Who may be able to participate

Inclusion Criteria: * Signed informed consent prior to initiation of study-related procedures * Age 21 - 80 years * Weight \< 205 kgs * ECOG ≤ 1 * Diagnosed with histologically confirmed lung cancer, regardless of disease stage and receiving any prior line of any therapy in the context of metastatic disease * An interval of at least three months following the completion of primary resection, if appropriate * An interval of no longer than ten years following completion of primary therapy, if appropriate * Life expectancy ≥ 4 months * Performing less than 150 minutes of structured moderate-intensity or strenuous-intensity exercise per week * Exercise intolerance (i.e., patients must have a VO2peak below that predicted for active age and sex-matched individuals) * Willing to be randomized to one of the study arms * Willing to commit to the study program and comply with all related protocol procedures * Able to achieve an acceptable peak baseline CPET, as defined by any of the following criteria: * achieving a plateau in oxygen consumption, concurrent with an increase in power output; * a respiratory exchange ratio ≥ 1.10; * attainment of maximal predicted heart rate (HRmax) (i.e., within 10 bpm of age-predicted HRmax \[HRmax = 220-Age\[years\]); * volitional exhaustion, as measured by a rating of perceived exertion (RPE) ≥ 18 on the BORG scale. * Able to complete an acceptable baseline CPET in the absence of high risk ECG findings or other inappropriate response to exercise as determined by the PI. * Ability to achieve and complete an acceptable baseline one-repetition maximum muscular strength test as defined by the effective execution of protocol-specific joint and muscle ranges of motion without remarkable signs or symptoms of pain, discomfort or distress. Exclusion Criteria: * Presence of a concurrent, actively treated other malignancy, or history of other malignancy treated within the past 3 years (other than non-melanoma skin cancer); * Room air desaturation at rest ≤ 85%; * Mental impairment leading to inability to cooperate. * Any of the following absolute contraindications to cardiopulmonary exercise testing: * Acute myocardial infarction (within 3-5 days of any planned study procedures); * Unstable angina; * Uncontrolled arrhythmia causing symptoms or hemodynamic compromise; * Recurrent syncope; * Active endocarditis; * Acute myocarditis or pericarditis; * Symptomatic severe aortic stenosis; * Uncontrolled heart failure; * Acute (within 3 months) pulmonary embolus or pulmonary infarction; * Thrombosis of lower extremities; * Suspected dissecting aneurysm; * Uncontrolled asthma; * Pulmonary edema; * Respiratory failure; * Acute non-cardiopulmonary disorders that may affect exercise performance or be aggravated by exercise (i.e., infection, renal failure, thyrotoxicosis)

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • Memorial Sloan Kettering Cancer CenterNew York, New York

Source and freshness
Processed from ClinicalTrials.gov. Last public update: May 4, 2025. Always confirm current availability with the study team.

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