Adapted Physical Activity (APA) in a Breast Cancer Population.

Quality of Life Clinical Trial

Official title:

Adapted Physical Activity (APA), Insulin Resistance, Oxidative Stress and Microcirculatory Haemodynamics in Breast Cancer Patients.

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT03528473
• Other study ID #: APA-PG1
• Status: Active, not recruiting
• Phase: N/A
• Start date: January 1, 2019
• Est. completion date: December 31, 2022

Study information

• Verified date: September 2021
• Source: University Of Perugia
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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 information / eligibility

• Status: Active, not recruiting
• Enrollment: 100
• Est. completion date: December 31, 2022
• Est. primary completion date: December 31, 2022
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years to 80 Years

Eligibility

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)

Related Conditions & MeSH terms

• Atherosclerosis
• Breast Neoplasms
• Exercise
• Exercise Therapy
• Insulin Resistance
• Microcirculation
• Oxidative Stress
• Quality of Life

Intervention

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.

Locations

Country	Name	City	State
Italy	University of Perugia	Perugia

Sponsors (1)

Lead Sponsor	Collaborator
University Of Perugia

Country where clinical trial is conducted

Italy, 

References & Publications (5)

Adraskela K, Veisaki E, Koutsilieris M, Philippou A. Physical Exercise Positively Influences Breast Cancer Evolution. Clin Breast Cancer. 2017 Oct;17(6):408-417. doi: 10.1016/j.clbc.2017.05.003. Epub 2017 May 19. Review. — View Citation

Foucaut AM, Berthouze-Aranda SE, Touillaud M, Kempf-Lépine AS, Baudinet C, Meyrand R, Carretier J, Bachmann P, Fervers B. Reduction of health risk factors through an adapted physical activity program in patients with breast cancer. Support Care Cancer. 2014 Apr;22(4):1097-104. doi: 10.1007/s00520-013-2065-3. Epub 2013 Dec 3. — View Citation

Franses JW, Edelman ER. The evolution of endothelial regulatory paradigms in cancer biology and vascular repair. Cancer Res. 2011 Dec 15;71(24):7339-44. doi: 10.1158/0008-5472.CAN-11-1718. Epub 2011 Dec 5. Review. — View Citation

Tesarova P, Kalousova M, Zima T, Suchanek M, Malikova I, Kvasnicka J, Duskova D, Tesar V, Vachek J, Krupickova-Kasalova Z, Malik J. Endotelial activation and flow-mediated vasodilation in young patients with breast cancer. Neoplasma. 2013;60(6):690-7. doi: 10.4149/neo_2013_088. — View Citation

Ye J, Jia J, Dong S, Zhang C, Yu S, Li L, Mao C, Wang D, Chen J, Yuan G. Circulating adiponectin levels and the risk of breast cancer: a meta-analysis. Eur J Cancer Prev. 2014 May;23(3):158-65. doi: 10.1097/CEJ.0b013e328364f293. Review. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in physical activity levels	Self reported physical activity, using IPAQ-SF (International Physical Activity Questionnairev - Short Form) score	Evaluation baseline and after 6, 12 and 24 months from enrollment.
Primary	Change in BMI	Reduction of BMI expressed as body mass (kg) / height^2 (m^2)	Evaluation baseline and after 6, 12 and 24 months from enrollment.
Secondary	Change in Post-Occlusive Reactive Hyperemia (PORH)	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).	Evaluation baseline and after 6, 12 and 24 months from enrollment.
Secondary	Carotid intima-media thickness (IMT)	Improvement of macrovascular structures, that will be explored by carotid intima-media thickness (IMT) (two-dimensional B-mode ultrasonography), measured in mm.	Evaluation baseline and after 6, 12 and 24 months from enrollment.
Secondary	Arterial stiffness	Reduction of arterial stiffness, that will be evaluated by radial applanation tonometry (SphygmoCor) and general transfer function assessing PWV (measure in m/s).	Evaluation baseline and after 6, 12 and 24 months from enrollment.
Secondary	Hemorheological profile	Improvement of Hemorheological profile, that will be studied with Serum, Plasma, and Blood Viscosity (Haake rotational viscometer), measured as mPas.	Evaluation baseline and after 6, 12 and 24 months from enrollment.
Secondary	Serum adiponectin	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.	Evaluation baseline and after 6, 12 and 24 months from enrollment.
Secondary	Serum IGF-1	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.	Evaluation baseline and after 6, 12 and 24 months from enrollment.
Secondary	VFA (Visceral Fat Area)	Improvement of Ultrasound assesment of visceral fat area (VFA, by MyLab 50 Ultrasonography, Esaote), measured by Hirooka formula (cm^2)	Evaluation baseline and after 6, 12 and 24 months from enrollment.
Secondary	HOMA-IR index	Homeostatic model assessment (HOMA) for insulin resistance (IR) is a method for assessing ß-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.	Evaluation baseline and after 6, 12 and 24 months from enrollment.
Secondary	Maximal aerobic capacity (VO2max)	Increase of maximal aerobic capacity after physical training, measured as ml/kg/min.	Evaluation baseline and after 6, 12 and 24 months from enrollment.
Secondary	miRNA	Variation of serum miR-10b, 15a, 146, 155, 375 e let-7a,b,c concentrations.	Evaluation baseline and after 6, 12 and 24 months from enrollment.