breast cancer. Malignant neoplasm of breast
Conditions
Interventions
Intervention 1: Intervention group: Depression, quality of life and demographic questionnaires will be completed as a pre-test. The written consent of the research firm is obtained from them. Motion t
Sponsors
Mazandaran University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: women with breast cancer Non-metastatic non-postmenopausal over 18 years of age at least literate one or both breast drains The drain has been removed no psychological treatment experience no drug addiction No heart disease No respiratory disease no history of regular physical activity one year prior to the study patient consent to participate in research and written consent
Exclusion criteria
Exclusion criteria: Subject's unwillingness to continue the intervention physical disability of the intervention due to treatment periods Unable to walk Unable to stand People with a HADS questionnaire score of less than 11.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Quality of Life. Timepoint: Before intervention - 5 weeks later. Method of measurement: 1) QLQ-C30 specific quality of life questionnaire and 2 quality of life questionnaire for breast cancer patients: EORTC QLQ-C23.V.3.;Depression and anxiety. Timepoint: Before intervention - 5 weeks later. Method of measurement: HADS Hospital Expression and Anxiety Questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Level of physical fitness. Timepoint: Before surgery, after drainage, 5 weeks later. Method of measurement: 6 minute walk test.;Joint angles and axis view of joint motion. Timepoint: Goniometer. Method of measurement: Before surgery, after drainage, 5 weeks later. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFahimeh Ghasemi Cherati
Mazandaran University of Medical Sciences
Outcome results
None listed