Quality of Life
Conditions
Interventions
This is a non-randomized clinical trial involving 20 women undergoing chemotherapy, divided into two groups. The experimental group (EG, n=10) participated in three weekly functional training sessions
OMNI-GSE 3 to 5), executed in three sets of 30 seconds with 30-second rest intervals between sets. The third phase comprised twenty-five minutes of strength training (neuromuscular 2
OMNI-GSE 5 to 7), also carried out in three sets of 30 seconds with 30-second rest periods. The final phase included five minutes of cardiometabolic training (OMNI-GSE 7 to 10), initially performed in
Sponsors
Programa de Pós-Graduação em Educação Física - PPGEF
Programa de Pós-Graduação em Educação Física - PPGEF
Eligibility
Sex/Gender
Female
Age
18 Years to 50 Years
Inclusion criteria
Inclusion criteria: Women diagnosed with HER2+ breast cancer (negative, positive, and/or triple positive for hormonal receptors);aged between 18 and 50 years;chemotherapy treatment conducted with monoclonal antibodies and/or their derivatives with the first cycle completed or ongoing;who have medical clearance to undergo the intervention protocol;normocardic;normotensive;with a ventricular ejection fraction above 50%;sedentary in the last three months prior to the start of the intervention protocol;without cognitive; functional;neuronal deficits;signing the informed consent form (ICF)
Exclusion criteria
Exclusion criteria: Women who have other types of diagnosed neoplasms;with metastatic lesions;who have undergone bilateral mastectomy;who receive chemotherapy treatment with anthracyclines alone;who change the type of chemotherapy during the application of the intervention protocol;who undergo only radiotherapy and/or hormone therapy;women with a diagnosis of previous cardiovascular disease;who have more than 25% absence in the intervention protocol;and those who die during the course of the protocol
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to observe a long-term cardioprotective effect provided by functional training in women diagnosed with breast cancer undergoing chemotherapy, during the pre- and post-intervention period over 3 months | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected to observe an improvement in functional capacity, quality of life, sleep quality, and muscle strength both in the pre-intervention and post-intervention periods | — |
Countries
Brazil
Contacts
Public ContactAna Luiza Setton
Programa de Pós-Graduação em Educação Física - PPGEF
Outcome results
None listed