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Lung Cancer, Exercise and Force Development

Exercise in Lung Cancer Patients - Specific Training, Muscle Mass and Force Development

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05778136
Enrollment
20
Registered
2023-03-21
Start date
2023-03-31
Completion date
2023-12-01
Last updated
2023-04-13

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

Conditions

Lung Cancer

Keywords

Exercise, Functionality, Resistance training, Muscle, skeletal, Sarcopenia

Brief summary

This study evaluates the effectiveness of a supervised one-leg resistance training program in patients with inoperable lung cancer with the primary outcome being rate of force development. Study design: Single center, two-armed, parallel-group, randomized controlled trial. The primary outcome being rate of force development after 12 weeks of progressive resistance training.

Detailed description

Muscular dysfunction and sarcopenia are known phenomena in cancer patients, and patients experience reduced muscle function and muscle loss regardless of cancer type or stage. Studies indicate that there are a number of cancer-specific and non-cancer-specific factors that influence muscle dysfunction, such as age, poor nutrition, physical inactivity, cancer pathology and treatment preparations. The decreased muscle function can ultimately lead to cachexia, typically seen in stage III - IV lung cancer patients. Previous studies have focused on 1-RM tests, muscle mass and functionality as outcomes. However, a central aspect of functionality in lung cancer patients may be the muscle's ability to develop force in a short time. The present study therefore has rate of force development as a primary outcome with muscle mass and functionality as supporting outcomes. In addition, the patients in this study will perform one-leg resistance exercise with the other leg as the control leg. This will eliminate the interpersonal bias normally seen in randomized controlled trials.

Interventions

OTHERResistance training

Supervised resistance training. 2 sessions/week for 12 weeks. The exercises are one-legged leg-press and one-leg knee extension. Resistance training start-up phase comprises 3 sets of 10 repetitions in each of the two exercises with 50% of 1RM. Resistance training progressive phase comprises 3 sets (leg-press) of 5-8 repetitions (70-90% 1 RM) and 6 sets (knee extension) of 8 repetition (75% 1RM). Rest between sets: 3 minutes

Sponsors

Rigshospitalet, Denmark
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Outcomes Assessor)

Intervention model description

Parallel assignment. The participants will be randomized to either left or right leg resistance training.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* patients (men and women) from the age of 18 years and above; patients with lung cancer (NSCLC stage III - IV and SCLC ED); patients with performance stage 0-2 according to WHO criteria

Exclusion criteria

* Patients where the doctor has listed contraindications for physical activity in the medical record; documented bone and brain metastases; persistent medullary plasia; patients on anticoagulation treatment; diagnosed symptomatic cardiac disease, including clinical congestive heart disease, arrhythmia requiring treatment or diagnosed myocardial infarction within the last three months; pericardial exudate; patients in terminal treatment; senile dementia and psychotic patients.

Design outcomes

Primary

MeasureTime frameDescription
Muscle strength/function: Rate of Force Development (RFD)Baseline, 6 weeks, 12 weeksThe between group change in Rate of Force Development (Nm/s) of the knee extensors. Assessed in the CON-TREX MJ dynamometer.

Secondary

MeasureTime frameDescription
Lean leg massBaseline, 6 weeks, 12 weeksThe between group change in lean leg mass (kg) assessed by whole-body dual-energy x-ray absorptiometry (DXA) scan
Functionality: Postural balanceBaseline, 6 weeks, 12 weeksPostural one-leg balance on a 5-cm high, 3-cm wide, and 50-cm long plastic bar. Between group change in number of times the participants steps off the bar or needs support to prevent falling in a period of 1 min.
Functionality: Sit-to-stand (30s STS)Baseline, 6 weeks, 12 weeksChange in sit-to-stand in 30 seconds
Functionality: 6 minutes walk test (6-MWT)Baseline, 6 weeks, 12 weeksChange in walking distance
Muscle strength/function: 1 RMBaseline, 6 weeks, 12 weeksThe between group change in 1 repetition maximum in knee-extension and leg-press
Muscle strength/function: PowerBaseline, 6 weeks, 12 weeksThe between group change in maximum isometric knee extension power (Nm). Assessed in the CON-TREX MJ dynamometer.
Muscle strength/function: Isokinetic strengthBaseline, 6 weeks, 12 weeksThe between group change in maximum isokinetic knee extension power (Nm) (60 degrees/s). Assessed in the CON-TREX MJ dynamometer.
Functionality: Sit-to-stand (5reps STS)Baseline, 6 weeks, 12 weeksChange in time for 5 STS repetitions

Countries

Denmark

Contacts

Primary ContactMorten Quist, ph.d.
morten.quist@regionh.dk+4535457335

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026