Adapted Physical Activity (APA) in a Breast Cancer Population.
- Conditions
- MicrocirculationExercise TherapyInsulin ResistanceAtherosclerosisBreast NeoplasmsExerciseOxidative StressQuality of Life
- Interventions
- Other: Exercise
- Registration Number
- NCT03528473
- Lead Sponsor
- University Of Perugia
- Brief Summary
The aim of this study is to investigate the effect of a 6-months program of Adapted Physical Activity (APA) on lifestyle, physical activity levels, insulin resistance and adipokines, oxidative stress, microcirculatory haemodynamics and serum levels of specific circulating miRNA in post-menopausal, physically inactive breast cancer patients in oncologic follow-up with or without hormone therapy that had completed adjuvant treatment (radiotherapy and/or chemotherapy) .
Furthermore, the study will determine the impact of APA on functional capabilities, on self-reported physical activity, quality of life and psychic health.
- Detailed 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.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- Female
- Target Recruitment
- 100
- 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)
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)
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Exercise Exercise Patients involved in the 6 months-physical training group.
- Primary Outcome Measures
Name Time Method Change in BMI Evaluation baseline and after 6, 12 and 24 months from enrollment. Reduction of BMI expressed as body mass (kg) / height\^2 (m\^2)
Change in physical activity levels Evaluation baseline and after 6, 12 and 24 months from enrollment. Self reported physical activity, using IPAQ-SF (International Physical Activity Questionnairev - Short Form) score
- Secondary Outcome Measures
Name Time Method Serum adiponectin Evaluation baseline and after 6, 12 and 24 months from enrollment. Improvement of serum adiponectin, measured by ELISA-method (ng/ml). Blood samples will be collected in the morning between 7:00 and 9:00 am, after overnight fasting.
Change in Post-Occlusive Reactive Hyperemia (PORH) Evaluation baseline and after 6, 12 and 24 months from enrollment. Improvement of Area of Hyperemia (AH) at Post-Occlusive Reactive Hyperemia (PORH) on Laser Doppler velocimetry (Periflux System 5000, Perimed), expressed as Perfusion Units (PU).
Serum IGF-1 Evaluation baseline and after 6, 12 and 24 months from enrollment. Improvement of serum IGF-1, measured by ELISA-method (ng/ml). Blood samples will be collected in the morning between 7:00 and 9:00 am, after overnight fasting.
VFA (Visceral Fat Area) Evaluation baseline and after 6, 12 and 24 months from enrollment. Improvement of Ultrasound assesment of visceral fat area (VFA, by MyLab 50 Ultrasonography, Esaote), measured by Hirooka formula (cm\^2)
Carotid intima-media thickness (IMT) Evaluation baseline and after 6, 12 and 24 months from enrollment. Improvement of macrovascular structures, that will be explored by carotid intima-media thickness (IMT) (two-dimensional B-mode ultrasonography), measured in mm.
Arterial stiffness Evaluation baseline and after 6, 12 and 24 months from enrollment. Reduction of arterial stiffness, that will be evaluated by radial applanation tonometry (SphygmoCor) and general transfer function assessing PWV (measure in m/s).
HOMA-IR index Evaluation baseline and after 6, 12 and 24 months from enrollment. Homeostatic model assessment (HOMA) for insulin resistance (IR) is a method for assessing β-cell function and insuline resistance from basal (fasting) glucose and insulin or C-peptide concentrations. HOMA-IR can be calculated with a simple mathematical approximation as HOMA-IR = (FPI × FPG)/22.5, where FPI is fasting plasma insulin concentration (mU/l) and FPG is fasting plasma glucose (mmol/l), or as HOMA-IR = (FPI × FPG)/405 if fasting plasma glucose is expressed in mg/dl.
Values bethween 3 and 5 are considered expression of moderate insuline resistance; values upper 5 are considered expression of severe insuline resistance.
Improvement of insulin-sensitivity expressed as HOMA-IR index reduction.Maximal aerobic capacity (VO2max) Evaluation baseline and after 6, 12 and 24 months from enrollment. Increase of maximal aerobic capacity after physical training, measured as ml/kg/min.
miRNA Evaluation baseline and after 6, 12 and 24 months from enrollment. Variation of serum miR-10b, 15a, 146, 155, 375 e let-7a,b,c concentrations.
Hemorheological profile Evaluation baseline and after 6, 12 and 24 months from enrollment. Improvement of Hemorheological profile, that will be studied with Serum, Plasma, and Blood Viscosity (Haake rotational viscometer), measured as mPas.
Trial Locations
- Locations (1)
University of Perugia
🇮🇹Perugia, Italy