Therapeutics
Conditions
Interventions
This is uncontrolled clinical trial, a single-arm, single-centre. Experimental group: 30 children and adolescents diagnosed with cancer who are undergoing cancer treatment will receive a physical acti
G11.427.410.698.277
Sponsors
Universidade Federal de Santa Catarina
Universidade Federal de Santa Catarina
Eligibility
Age
4 Years to 14 Years
Inclusion criteria
Inclusion criteria: Have been diagnosed with cancer; Children and adolescents aged between 4 and 15 years old, of both sexes; Being undergoing outpatient cancer treatment at Joana de Gusmão Children's Hospital; Who are at any stage of treatment; Performing any type of cancer treatment (Chemotherapy, Radiotherapy, surgery, among others); Who present cognitive conditions to participate in the research, which will be evaluated from the direct observation of the researchers, in contact with the parents; That present motor conditions to carry out the tests of strength production capacity and functional capacity
Exclusion criteria
Exclusion criteria: Neuromotor impairment; The medical team considers it unfeasible; Momentary incapacity that makes it impossible for them to perform the pre-intervention assessment or that, at the time of the anamnesis, some incapacity is verified, such as (extreme tiredness, malaise, discomfort); Parents or patients refuse to sign the consent form;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find an improvement in Cancer-Related Fatigue (CRF), evaluated by the Pediatric Quality of life inventoryTM Multidimensional Fatigue Scale (PedsQLTM Multidimensional Fatigue Scale) ((PedsQL) Multidimensional Fatigue Version) (PedsQL-MFS), with an improvement of at least 10% in the FRC. Data collected before and after the intervention. | — |
Secondary
| Measure | Time frame |
|---|---|
| Expect to find an improvement in Isometric Force Production Capability with an improvement of at least 10% in Isometric Force Production. Data collected before and after the intervention. A microFET2 HHD manual dynamometer (Hoggan Health Industries, Salt Lake City, Utah) will be used.;It is expected to find an improvement in Functional Capacity with an improvement of at least 10% in Functional Capacity. Data collected before and after the intervention. The Timed Up and Go (TUG) test will be used.;The Sedentary Behavior will be used for the initial evaluation, the questionnaire used will be To evaluate the sedentary behavior (CS) the procedure adopted by Costa & Assis (2011) will be used. Through a Questionnaire, applied to the parents or guardians of the participants, information about the average time exposure using screens (television, video game and computer use), on typical weekdays and typical weekend days will be required. It is assumed that with the intervention, the level of CS will increase. | — |
Countries
Brazil
Contacts
Public ContactLicelli Cardoso
Universidade Federal de Santa Catarina
Outcome results
None listed