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Fitness, Activity and Lung Cancer Study

Cardiorespiratory Fitness and Effect of Training After Lung Cancer Surgery. A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01748981
Acronym
FALC
Enrollment
71
Registered
2012-12-13
Start date
2010-11-30
Completion date
2018-06-20
Last updated
2019-02-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lung Cancer

Keywords

Pulmonary function, Maximal oxygen uptake, Cardiorespiratory fitness, High-intensity training, Surgery

Brief summary

The purpose of the study is to investigate the change in pulmonary function and exercise capacity in lung cancer patients after pulmonary resection. Furthermore, to study the effect of training on aerobic capacity, muscular strength, morbidity and survival. Physical activity level by accelerometers, body composition by DXA and quality of life will also be reported.

Detailed description

Five year after surgery, all included patients will be reinvited to undergo a fourth health excame to study the long-term effects of exercise training on physical fitness, morbidity and survival.

Interventions

OTHERPhysical training

Physical training three times a week for 20 week including endurance and strength training compare to the as usual group as controls

Controls, not training

Sponsors

Norwegian School of Sport Sciences
CollaboratorOTHER
University Hospital, Akershus
CollaboratorOTHER
Vestre Viken Hospital Trust
CollaboratorOTHER
Oslo University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
30 Years to 79 Years
Healthy volunteers
No

Inclusion criteria

* Non smal cell lung cancer * Patient living in Oslo or Akershus county and accepted for lung cancer surgery at Oslo University hospital and Akershus University hospital * were able to read and speak Norwegian

Exclusion criteria

* Mental incompetence or physical disability that makes it difficult to walk on a treadmill * Treatment or medical complications affecting ability to participate in an exercise group * \> 79 years

Design outcomes

Primary

MeasureTime frameDescription
Change in Maximal oxygen uptake (VO2max) from baselineAn expected average of two weeks before surgery (baseline), four to six weeks after surgery, after six months and after 5 yearsChange in VO2max from before to after surgery to measure the effect of surgery, and after six months to measure the effect of high-intensity training intervention, and after five years to study long-term effects

Secondary

MeasureTime frameDescription
Change in Pulmonary function from baselinePulmonary function is measured three times; an expected average of two weeks before surgery, four to six weeks after surgery, after after six months and after five years.Change in pulmonary function from before to after surgery and after the intervention

Other

MeasureTime frameDescription
DXA scanAn expected average of two weeks before surgery, four to six weeks after surgery, after six months and after five yearsChange in body composition from before to after surgery and after the intervention
Quality of lifeMeasured three times: An expected average of two weeks before surgery, four to six weeks after surgery, after six months and after five yearsChange in quality of life from before to after surgery and after the intervention
Physical activityMeasured three times: six weeks after surgery, after six months and after five yearsPhysical activity will be objectively measured by accelerometers for seven consecutive days to determine change in activity level after surgery

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026