Skip to content

The Effect of Resistance Training and Aerobic Training on Body Composition During Chemotherapy

The Effect of Resistance Training and Aerobic Training on Body Composition During Chemotherapy

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02192216
Enrollment
16
Registered
2014-07-16
Start date
2014-02-28
Completion date
2016-12-31
Last updated
2018-03-01

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

Conditions

Neoplasms

Keywords

Body composition, Chemotherapy, Muscle mass, Muscle function, Exercise

Brief summary

Chemotherapy can induce muscle loss in colorectal, breast and advanced renal cell carcinoma patients. The Danish nation-wide training and rehabilitation offer 'Body & Cancer' offers intensive resistance and endurance training to all Danish cancer patients receiving chemotherapy with the aim of reducing treatment-related fatigue and physical impairments, but the potential of the training to preserve or improve muscle mass is uninvestigated. Furthermore, the underlying biological mechanisms of treatment and/or exercise induced changes in muscle mass in cancer patients remains uninvestigated. Thus, the primary purpose of the present study is to investigate changes in body composition during chemotherapy and after resistance and aerobic training combined with protein supplementation during ongoing chemotherapy in cancer patients. Secondly, we aim to investigate the underlying biological mechanisms of muscle mass regulation in biopsies obtained before and after a control period as well as after 10 weeks of exercise, both during chemotherapy. We hypothesize that 10 weeks exercise will improve muscle mass and body composition in cancer patients during chemotherapy as compared to a control period during chemotherapy alone.

Interventions

BEHAVIORALExercise

Sponsors

Aarhus University Hospital
CollaboratorOTHER
Department of Public Health, Denmark
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

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

Inclusion criteria

* Currently receiving curative, adjuvant, neo-adjuvant or palliative chemotherapy * No documented bone metastases or myelomatosis * No documented CNS affection * WHO performance status 0-1 * No chronical thrombocytopenia or leukopenia * No physical conditions preventing exercise participation * No serious symptoms of heart disease * No dementia or mental illness preventing participation * Signed written concent * Age above 18 years

Exclusion criteria

* Participation in systematic resistance training three months prior to inclusion

Design outcomes

Primary

MeasureTime frameDescription
Changes in body compositionAssessment before (baseline) and after (pre-training) the control period of 7 weeks (average), where patients recieve chemotherapy, and again after completion of 10 weeks of exericse (post-training).Changes in lean body mass and fat mass wil be assessed using Dual Energy X-Ray Absorptiometry

Secondary

MeasureTime frameDescription
Changes in underlying biological mechanisms associated with changes in muscle massAssessment before (baseline) and after (pre-training) the control period of 7 weeks (average), where patients recieve chemotherapy, and again after completion of 10 weeks of exericse (post-training).Analyzed from muscle biopsies from m. vastus lateralis and venous blood samples
Changes in dynamic muscle strengthAssessment before (baseline) and after (pre-training) the control period of 7 weeks (average), where patients recieve chemotherapy, and again after completion of 10 weeks of exericse (post-training).Changes in muscle strength will be assessed using 1 repetition maximum (kg) tests using conventional training equipment.
Changes in aerobic performanceAssessment before (baseline) and after (pre-training) the control period of 7 weeks (average), where patients recieve chemotherapy, and again after completion of 10 weeks of exericse (post-training).Changes in aerobic performance will be assessed using the Watt max bicycle ergometer test. Maximal oxygen consumption (L O2 pr min) will be estimated based on this test.
Changes in cancer related fatigue and quality of lifeAssessment before (baseline) and after (pre-training) the control period of 7 weeks (average), where patients recieve chemotherapy, and again after completion of 10 weeks of exericse (post-training).Changes in cancer related fatigue and quality of life wil be assessed using the European Organisation for Research and Treatment of Cancer (EORTC) questionaire QLQ C30
Changes in functional performanceAssessment before (baseline) and after (pre-training) the control period of 7 weeks (average), where patients recieve chemotherapy, and again after completion of 10 weeks of exericse (post-training).Changes in functional performance will be assessed using various validated functional performance tests. Thus, changes will be asssessed in 30 s arm curl test (max repetitions) , 30 s chair rise test (max repetitions), stair climbing test (time to ascend to flights of stairs), 10 m maximal gait speed test (time to walk 10 m as fast as possible).

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 3, 2026