Breast cancer, Quality of life, Fatigue, Lymphedema, Depression, Range of Motion, Articular.
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients older than 18 years; Diagnosis of clinical stage I to III of breast cancer; Being in the period of adjuvant treatment with chemotherapy, radiotherapy or hormone therapy; And receive the release of the oncologist responsible for the practice of physical activity, as well as the Physical Therapy Sector of CEPON.
Exclusion criteria
Exclusion criteria: Patients that present some orthopedic or neurological limitation that prevents the practice of physical activity.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Quality of Life Questionnaire C30 (EORTC QLQ-C30 and EORTC QLQ-BR23) before (baseline) and after intervention, and three months, six months, 12 months and 24 months after finish intervention. | — |
Secondary
| Measure | Time frame |
|---|---|
| (2) Psychological factors: Depressive symptoms will be investigated using the Beck Depression Inventory (BDI); Body image, will be approached by the Body Image After Breast Cancer (BIBCQ) questionnaire; For the investigation of self-esteem, the Self-Esteem Scale (EAR) developed by Rosenberg (1965) will be used; The optimism will be evaluated through the Instrument of Life Orientation Test (TOV-R); Stress will be investigated by the Perceived Stress Scale. Developed by Cohen; Kamarck; Mermelstein (1983); Fatigue, will be investigated by the Functional Assessment of Cancer Therapy-Fatigue instrument (FACT-F); The sexual function will be identified by the Female Sexual Function Index (FSFI) with cross-cultural validation by Thiel et al. (2008); Sleep quality will be assessed by the Pittsburgh Sleep Quality Index. Validated by Bertolazzi et al., (2011); In order to investigate patients' pain, the Visual Analogue Scale (EVA) will be used. ;(3) Physical factors: Cardiorespiratory fitness will be evaluated by the submaximal exertion test (75% of maximum heart rate-HRmax) in treadmill; Additionally, we will also use the 6-minute Test; (IPAQ - short version) (PARDINI et al., 1997) and the use of the ActiGraph wGT3X-BT accelerometer (Pensacola et al., 1997). , FL, USA); The Upper limb functionality will be evaluated through the Disabilities of the Arm, Shoulder and Hand (DASH) scale developed by Hudak et al. (1996); The muscular strength of the upper limb will be measured by the apparatus Digital portable dynamometer Chatillôn; To verify the range of motion, evaluations of flexion, extension, abduction, adduction, external rotation and internal rotation of the shoulder will be performed through the use of the Carci goniometer; The postural evaluation will be carried out through the Postural Evaluation Software SAPO, which is a freely distributed software under the terms of the GNU General Public License; For the flexibility test the "sit and reach" test will be used through | — |
Countries
Brazil
Contacts
Universidade do Estado de Santa Catarina;Universidade do Estado de Santa Catarina