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临床试验/NCT01795612
NCT01795612已完成不适用

Adapted Physical Activity Effect on Aerobic Function and Fatigue at Home in Patients With Breast Cancer Treated in Adjuvant or Neoadjuvant Phase

University Hospital, Limoges2 个研究点 分布在 1 个国家目标入组 94 人开始时间: 2013年3月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
94
试验地点
2
主要终点
The main criterion is exercise tolerance at 12 months measured by VO2peak by incremental cardiopulmonary exercise test

研究概览

简要总结

Physical exercise has been identified as a major item of many chronic diseases and cancer rehabilitation. It contributes to an improvement in the quality of life and to a decrease in the current treatment side effects and mortality. Cancer in association with treatment toxicity and an inactive lifestyle lead to a fall in physical capability and causes problems in daily activities. The physical capacity and the tolerance for exercise fall simultaneously leading to a deconditioning vicious circle which increases physical, psychological and emotional symptoms of fatigue. Therefore, physical activity for health is a valid and relevant way to improve quality of life and to manage cancer patient fatigue. The aim of the study is the assessment of the effects of a physical activity retraining program on aerobic capacity, strength and fatigue, in a breast cancer population treated by adjuvant or néoadjuvant chemotherapy.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • females between 18 and 75 years of age;
  • signed written informed consent;
  • willing to take part in the trial and to follow the instructions;
  • breast tumour, histologically documented;
  • patients for whom a 6-treatment course of adjuvant or neoadjuvant chemotherapy (3FEC100 +3 taxanes or 6 FEC) +/- radiotherapy+/- Herceptin has been scheduled;

排除标准

  • metastatic cancer;
  • disability preventing a proper understanding of the instructions for the trial;
  • patients who are subject to a court protection, wardship or guardianship order;
  • uncontrolled hypertension;
  • family history of sudden death in a first-degree relative;
  • unstabilised heart disease;
  • current treatment with beta-blockers;
  • chronic or acute pulmonary disease associated with dyspnoea upon moderate effort;
  • uncontrolled thyroid dysfunction;
  • uncontrolled diabetes;
  • any other serious conditions that are unstabilised,
  • disabling or in which physical exercise is contra-indicated;
  • unable to attend for follow-up throughout the duration of the study;
  • ventricular ejection fraction (VEF) < 50%, pregnancy or suckling.

研究组 & 干预措施

Arm A

Other

6-month ETP, during adjuvant or neoadjuvant therapy

干预措施: physical activity (Other)

Arm B

Other

6-month ETP, after adjuvant or neoadjuvant therapy

干预措施: physical activity (Other)

Arm C

Other

12-monthETP, during and after adjuvant or neoadjuvant treatment

干预措施: physical activity (Other)

结局指标

主要结局

The main criterion is exercise tolerance at 12 months measured by VO2peak by incremental cardiopulmonary exercise test

时间窗: at 12 months

unit of measure:ml/kg/min

次要结局

  • Exercise tolerance at 12 months (group A vs B)(at 12 months)

研究者

发起方
University Hospital, Limoges
申办方类型
Other
责任方
Sponsor

研究点 (2)

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