Adapted Physical Activity (APA) in a Breast Cancer Population.
Keywords
Abstract
Description
This is a randomized controlled double-group assignment study with intermedial switch-over including post-menopausal, physically inactive breast cancer patients in oncological follow-up with or without hormone therapy, that had completed adjuvant post-surgical treatment (radiotherapy and/or chemotherapy) from at least 3 months and from not more than 3 years.
Patients in hormonal therapy and patient not in hormonal therapy will be assigned in two different groups, each one of 50 patients. In each groups, patients will be randomized divided in a control group (25 pt) and in a 6 months-physical training group (25 pt). After 6-months patient in control group will be switched in the physical training group.
The duration of the study is 2 year. Clinical evaluation of the patients will be made: at the enrollment, after 6, 12, and 24 months.
Physical activity will be adapted according to arm and shoulder morbidity, after fracture risk assessment. Exercise will be concentrated solely on leg muscles (pedalling on a cycle or bed ergometer) in individuals with limitations in the range of motion of the arms (eg, due to breast, axillary, or thoracic surgery). In patients experiencing ataxia, dizziness, or peripheral neuropathy, walking outdoors and mostly cycle-ergometry training will be preferred to other activities that also involve large muscle groups but require additional balance and coordination (eg, treadmill walking, outdoor cycling).
Exercises will be performed at the Unipolar Spinal Unit of "S. Maria della Misericordia" Hospital, Perugia.
The aim of the study is to confirm the positive effect of APA on metabolic stress, body mass composition, functional capacity, serum levels of specific circulating miRNA and quality of life in breast cancer patients in oncological follow-up.
Currently, only few data are available about the relationship between physical activity and microcirculatory hemodynamics that, together with oxidative stress, could be involved in genesis and progression of breast cancer.
Dates
Last Verified: | 03/31/2020 |
First Submitted: | 03/21/2018 |
Estimated Enrollment Submitted: | 05/03/2018 |
First Posted: | 05/16/2018 |
Last Update Submitted: | 04/01/2020 |
Last Update Posted: | 04/02/2020 |
Actual Study Start Date: | 12/31/2018 |
Estimated Primary Completion Date: | 12/30/2022 |
Estimated Study Completion Date: | 12/30/2022 |
Condition or disease
Intervention/treatment
Other: Exercise
Phase
Arm Groups
Arm | Intervention/treatment |
---|---|
Experimental: Exercise Patients involved in the 6 months-physical training group. | Other: Exercise The exercise intervention consists of 60 minutes sessions, divided into 40 minutes of aerobic exercise and 20 minutes of circuit training for muscular strength and flexibility exercises.
Aerobic exercise is performed using treadmill, exercise bikes, syncro and arm-ergometers, gradually increasing the exercise intensity, after a 10 minutes period of warming-up, to 60-80 % of Maximum Heart Rate.
Resistance training consists of resistance exercises for large muscle groups, performed with body weight-exercises and isotonic machines. |
No Intervention: Control Patients in control group carry on their usual follow-up programme. |
Eligibility Criteria
Ages Eligible for Study | 18 Years To 18 Years |
Sexes Eligible for Study | Female |
Accepts Healthy Volunteers | Yes |
Criteria | Inclusion Criteria: - breast cancer patients in oncological follow-up - post-menopausal age - physically inactivity (light to moderate or vigorous leisure-time physical activity less than 10 minutes a day, US National Health Interview Survey) - assuming or not hormone therapy - after 3 months - 3 years from adjuvant post-surgical treatment (radiotherapy and/or chemotherapy) Exclusion Criteria: Permanent - Patients older than 80 years - Inability to carry on physical activity - Metastatic neoplasia or unknown stage and/or histology - Concomitant neoplasia - Patients on corticosteroid treatment - Known heart disease (heart failure NYHA II (New York Heart Association II) or superior, angina pectoris or positive exercise stress test, treatment-related cardiotoxicity) - Currently on a weight loss plan or on moderate physical activity before the start of the project (no more than three sessions a week) - Severe cachexia (loss of more than of 35% premorbid weight or weight loss more than 10% in the last 6 months). - Morbidly obesity (BMI >40 kg/m2), - Immunodepression (absolute neutrophils count < 500/mmc) Temporary - Uncontrolled pain or new onset bone pain until further diagnostic study - Severe anemia (haemoglobin below 8 g/dL) or platelet count lower than <50000/μL - Fever (temperature above 38ºC) or acute infections - Severe nausea and vomiting within previous 24-36 h - Uncontrolled blood pressure (systolic blood pressure > 160 mm Hg and/or diastolic blood pressure >99 mm Hg) |
Outcome
Primary Outcome Measures
1. Change in physical activity levels [Evaluation baseline and after 6, 12 and 24 months from enrollment.]
2. Change in BMI [Evaluation baseline and after 6, 12 and 24 months from enrollment.]
Secondary Outcome Measures
1. Change in Post-Occlusive Reactive Hyperemia (PORH) [Evaluation baseline and after 6, 12 and 24 months from enrollment.]
2. Carotid intima-media thickness (IMT) [Evaluation baseline and after 6, 12 and 24 months from enrollment.]
3. Arterial stiffness [Evaluation baseline and after 6, 12 and 24 months from enrollment.]
4. Hemorheological profile [Evaluation baseline and after 6, 12 and 24 months from enrollment.]
5. Serum adiponectin [Evaluation baseline and after 6, 12 and 24 months from enrollment.]
6. Serum IGF-1 [Evaluation baseline and after 6, 12 and 24 months from enrollment.]
7. VFA (Visceral Fat Area) [Evaluation baseline and after 6, 12 and 24 months from enrollment.]
8. HOMA-IR index [Evaluation baseline and after 6, 12 and 24 months from enrollment.]
9. Maximal aerobic capacity (VO2max) [Evaluation baseline and after 6, 12 and 24 months from enrollment.]
10. miRNA [Evaluation baseline and after 6, 12 and 24 months from enrollment.]