Movement and Health Beyond Care, MoviS: Nutrition and Exercise Educational Programs for Breast Cancer Survivors
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 172
- 试验地点
- 4
- 主要终点
- Quality of life assessed by questionnaire
研究概览
简要总结
MoviS is a randomized controlled trial on the effect of aerobic exercise training on quality of life (QoL) among breast cancer (BC) survivors.
Patients randomized to the intervention arm will receive lifestyle recommendations (nutrition and exercise) and will undergo the MoviS Training program, whereas control arm patients will receive lifestyle recommendations. The MoviS Training program consists of 3 months, 3 times per week, aerobic exercise, which will be supervised both directly (2 days each week) and remotely (1 day each week). Exercise intensity (40% to 70% of heart rate reserve) and duration (20 to 60 mins) will be gradually increased throughout the training period. Both arms will receive counseling on psychological well-being.
The primary outcome is the improvement of QoL. The secondary outcome is the improvement of the health-related parameters.
Study variables will be sampled and compared between and within groups at the baseline, after the 3 month intervention period, ad interim in the short term (6 months) and long term (12 and 24 months).
详细描述
BACKGROUND BC is the most common invasive cancer in women and evidence has shown that exercise can significantly improve the outcomes of BC survivors. MoviS (Movement and Health Beyond Care) is a randomized controlled trial that aims to evaluate the potential health benefits of exercise and proper nutritional habits.
Aim The present research study aims to assess the efficacy of aerobic exercise training on the QoL of high-risk BC survivors and the improvement of health-related factors.
Methods BC patients (sample size n=172), age 30-70 years, non-metastatic, stage 0-III, non-physically active, 6-12 months post-surgery, and post chemo- or radio-therapy, with a high risk of recurrence defined by one or more of the following criteria: BMI ≥ 25, diagnosis of metabolic syndrome, increased level of blood testosterone and insulin will be randomly allocated to the interventional arm (lifestyle recommendations and MoviS Training) or control arm (lifestyle recommendations). The MoviS Training consists of 3 months of aerobic exercise training (2 d/week of directly supervised and 1 d/week of remotely supervised exercise) with a progressive increase in exercise intensity (40-70% of heart rate reserve) and duration (20-60 min). Both arms will receive counseling on healthy lifestyle habits (nutrition and exercise) based on the World Cancer Research Fund (WCRF) 2018 guidelines through the DIANA-Web platform. All patients will also undergo psychological well-being counseling, which comprises evaluation for anxiety and depression.
The primary outcome is the improvement of the QoL assessed by the European Organization for Research and Treatment of Cancer QoL (EORTC QLQ-C30) questionnaire.
The secondary outcome is the improvement of health-related parameters such as: fatigue; anthropometric measurements and body composition; cardiac function indexes and heart rate variability; functional parameters (cardiorespiratory fitness, muscle flexibility and strength, coordination and posture variability, upper limb muscle viscoelastic characteristics); psychological well-being; metabolic, hormonal and inflammatory risk factors; gut microbiota; osteoporosis level; recurrences. Diet habits, physical activity level, pharmacological treatments and comorbidity will be recorded as confounding factors and covariates.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- None
入排标准
- 年龄范围
- 30 Years 至 70 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Diagnosis of BC (stage 0-II-III, without metastases or recurrences diagnosis at recruitment).
- •After surgery and chemotherapy and/or radiotherapy treatments.
- •Maximum 12 months from surgical treatment.
- •Minimum 6 months from the end of chemotherapy.
- •Risk of recurrence will be identified with meeting at least 1 of the following criteria: BMI at diagnosis ≥ 25 kg/m2, testosterone ≥ 0.4 ng/mL (for women); serum insulin ≥ 25 µU/mL (170 pmol/L); metabolic syndrome (at least 3 of the following 5 factors): a. glycemia ≥ 100 mg/dL (6.05 mmol/L); b. triglycerides ≥150 mg/dL (1.69 mmol L); c. HDL-C <50 mg/dL (1.29 mmol/L) (woman), <40 mg/dL (1.04 mmol/L) (man); d. waist circumference ≥ 80 cm (woman), ≥ 90 cm (man); e. blood pressure ≥ 130/85 mmHg.
- •Non-physically active: subjects who were not regularly active (assessed by IPAQ) for at least 6 months.
排除标准
- •Not suitable for non-competitive physical activity after the cardiological medical examination.
- •Disabling pneumological, cardiological, neurological, orthopedic comorbidities and mental illness that prevent the exercise performance.
- •Treatment with drugs that alter the heart rate response to exercise.
- •Treatment with antidepressant drugs.
结局指标
主要结局
Quality of life assessed by questionnaire
时间窗: Baseline - after 3, 6, 12, 24 months
Change in quality of life assessed by the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30). Scores ranging from 0 to 100; higher scores indicate better quality of life.
次要结局
- Anthropometry(Baseline - after 3, 6, 12, 24 months)
- Upper limb muscles viscoelastic characteristics(Baseline - after 3 months)
- Homeostatic Model Assessment for Insulin Resistance (HOMA-IR) Index(Baseline - after 3, 6, 12, 24 months)
- C-reactive protein(Baseline - after 3, 6, 12, 24 months)
- Osteoporosis level(Baseline - after 12 and 24 months)
- Cardiac function indexes(Baseline - after 3, 6, 12, 24 months)
- Cardiorespiratory fitness(Baseline - after 3, 6, 12, 24 months)
- Muscular fitness(Baseline - after 3, 6, 12, 24 months)
- Posture balance(Baseline - after 6 months)
- Fatigue(Baseline - after 3, 6, 12, 24 months)
- Body composition(Baseline - after 3, 6, 12, 24 months)
- Heart rate variability(Baseline - after 3 months)
- Flexibility(Baseline - after 3, 6, 12, 24 months)
- Proprioceptive recalibration(Baseline - after 6 months)
- Psychological well-being(Baseline - after 3, 6, 12, 24 months)
- Insulin-like growth factor (IGF-1)(Baseline - after 3, 6, 12, 24 months)
- Gut microbiota(Baseline - after 3, 6, 12, 24 months)
- Recurrences(Baseline - after 3, 6, 12, 24 months)
研究者
Elena Barbieri
Associate Professor
University of Urbino "Carlo Bo"
