Malignant neoplasm of breast
Conditions
Interventions
This is a randomized controlled, parallel, two-arm clinical study. The experimental group will be 15 women undergoing treatment for stage I to III breast cancer who will undergo a Yoga program twice a
G11.427.410.698.277
Sponsors
Universidade Federal de Pelotas
Universidade Federal de Pelotas
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: To participate in the sample, participants must meet the following eligibility criteria: age equal to or greater than 18 years; diagnosis of stage I-III breast cancer; undergoing chemotherapy or radiotherapy; if you are undergoing radiotherapy treatment, you have already completed chemotherapy treatment; not present a history of severe cardiovascular disease that prevents the practice of physical exercise (with the exception of arterial hypertension controlled by medication); no active metastatic or locoregional disease; not have any severe physical or psychiatric condition that makes it impossible to exercise and not be engaged in regular exercise programs for more than 75 minutes a week.
Exclusion criteria
Exclusion criteria: Be under the age of 18; have already completed Primary treatment for breast cancer; presenting active metastatic or locoregional disease; have a severe physical or psychiatric condition that makes it impossible to exercise, be engaged in regular physical exercise programs for more than 75 minutes a week.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find a difference in cancer-related fatigue levels in the intervention group, assessed by a fatigue scale applied by an evaluator. Data collected pre-intervention (week 0) and post-intervention (week 9). | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected to observe an increase in functional capacity in the intervention group, assessed through a battery of tests applied by an evaluator. Data collected pre-intervention (week 0) and post-intervention (week 9).;t is expected to observe an increase in the level of physical activity in the leisure domain. Data collected pre-intervention (week 0) and post-intervention (week 9).;It is expected to observe an increase in quality of life, assessed through a questionnaire administered by an evaluator. Data collected pre-intervention (week 0) and post-intervention (week 9).;It is expected to observe an improvement in pain levels assessed through a questionnaire administered by an evaluator. Data collected pre-intervention (week 0) and post-intervention (week 9). | — |
Countries
Brazil
Contacts
Public ContactStephanie Pinto
Universidade Federal de Pelotas
Outcome results
None listed