Cancer Survivors
Conditions
Keywords
Rehabilitation, Physical exercise, Return to work, Fatigue, Cancer survivors
Brief summary
The project is a non-randomized intervention study with group-based physical exercise. Cancer survivors who have participated in the rehabilitation program at the Center for Education and Rehabilitation are included in the study. The cancer and cancer treatment have led to patients struggling with physical, mental and social late effects which prevent them from functioning in everyday life and return to work. The purpose of the project is to investigate whether one municipal group training measure can help to lower the threshold for the user to maintain good exercise habits and return to work / everyday life, as well as the effect on the user's physical form and quality of life and the transition between health level and the body itself measure.
Interventions
BEHAVIORALExercise training
18 weeks supervised strength and aerobic exercise training.
Sponsors
Haukeland University Hospital
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* 18 years * Women and men * Regardless of cancer diagnosis * Resident in Bergen municipality * Finishes their rehabilitation at The Cancer Center for Education and Rehabilitation spring/summer 2019.
Exclusion criteria
* Patients who do not speak or understand Norwegian * Unable to express themselves in writing * Unable to perform basic daily tasks * Display cognitive disorder or severe emotional instability * Suffer from other debilitating illnesses / conditions that may inhibit physical exercise (heart failure, chronic obstructive pulmonary disease, orthopedic conditions, neurological disorders or the like) will be excluded from the study. -
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Objectively recorded physical activity level | 18 weeks | Change in objectively recorded physical activity level, measured with the SenseWear ™ Mini Armband (SWA) (BodyMedia Inc. Pittsburgh, PA, USA) as average minutes of moderate- to vigorous intensity physical activity (MVPA) from before intervention to after completion of the intervention. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change in maximal oxygen uptake measured by VO2max | 18 weeks | Change in VO2max, measured by a maximal incremental exercise test on a treadmill, from before training intervention to post training intervention. |
| Change in maximal strength | 18 weeks | Change in 1 repetition maximum strength in upper and lower body measured from before intervention and after completion of the intervention. |
| Change in quality of life measured by Short Form Health Survey (SF-36) | 18 weeks | Change in scores on the Short Form Health Survey (SF-36) from before intervention to after completion of the intervention. |
| Change in fatigue scores using the Chalder Fatigue Questionaire (FQ) | 18 weeks | Change in scores on the Chalder Fatigue Questionaire (FQ) from before intervention to after completion of the intervention. |
Countries
Norway
Outcome results
None listed