breast cancer cervix cancer colon cancer ovarian cancer testis cancer or lymphomas cancer
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients with histological confirmed primary breast, colon, ovarian, cervix, testis cancer or lymphomas with no indication of recurrent or progressive disease, who completed ((neo)adjuvant) chemotherapy with curative intention, are eligible for this study.
Exclusion criteria
Exclusion criteria: Patients who are not able to perform basic activities such as walking or biking, who show cognitive disorders or severe emotional instability, who are suffering from other disabling comorbidity that might hamper physical performance capacity ( e.g. heart failure, chronic obstructive pulmonary disease (COPD), orthopaedic conditions and neurological disorders), and patients who are unable to understand and read the Dutch language will be excluded from the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Cardiorespiratory fitness, muscle strength and fatigue. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcome variables include body composition and bone mineral density, health-related quality of life, physical activity level, satisfaction with the intervention, mood disturbances, sleep quality, functioning in daily life and return to work. | — |
Countries
Netherlands