New study: walking may ease crushing fatigue after lung cancer surgery
NCT ID NCT03724331
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a low-cost, portable exercise program for people with non-small cell lung cancer after surgery. The goal was to help them manage severe fatigue and improve their quality of life. 235 adults took part, and the program was designed to be safe and practical for nearly all patients.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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235 people
The number who actually took part.
- Started
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Jun 2019
- Finished
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Nov 2023
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Women and men * At least 18 years of age (Michigan) and 19 years of age in (Nebraska) * With suspected non-small cell lung cancer to be confirmed after surgery * Karnofsky Performance Status score of at least 70% * Thoracic surgeon approval pre- and post-surgery * Medically stable comorbid conditions allowing for non-small cell lung cancer surgery clearance * Has phone access capability * Able to speak and write English * Able to hear and speak for phone interviews * Owns a television * Lives within 2 hours driving distance of recruitment site Exclusion Criteria: * Severe impairment of sight, hearing, speaking * Active treatment for malignancy within past 3 months (other than non-melanoma skin cancer or long-term hormonal treatment for common cancers such as breast and prostate if disease is stable * Weight greater than 330 pounds * History of photosensitive seizures * Any condition or disorder that would impede safe participation as directed * Plans to relocate outside the area during the study period or unable to fully participate
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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University of Nebraska Medical Center
Omaha, Nebraska, 68198, United States
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Other studies related to the condition(s) this trial covers.
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