DRKS00023243已完成未知
Resistance training as prehabilitation exercise in Mamma-CA - PräMaCa
niklinik Köln, Centrum für integrierte Onkologie (CIO)0 个研究点目标入组 66 人开始时间: 2020年12月17日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 66
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized controlled study
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 one（—）
- 性别
- Female
入选标准
- •diagnosed breast cancer
- •at least 12 weeks prior to surgical therapy (breast-conserving therapy (BET) or radical mastectomy with axillary dissection)
- •neo-adjuvant chemotherapy or neo-adjuvant radio-chemotherapy
- •Written and valid declaration of consent from the patient
- •Age> = 18 years
排除标准
- •Neo-adjuvant radiotherapy alone
- •Second malignancies
- •WHO / ECOG performance status> 1
- •Life expectancy <5 months
- •ductal carcinoma
- •metastases
- •All illness situations that do not allow hypertrophy training, in particular:
- •o Clinically manifest heart failure (NYHA III-IV)
- •o Partial or global respiratory failure
- •o Permanent thrombocytopenia <10,000 / µl, e.g. refractory autoimmune thrombocytopenias.
- •o Congenital or acquired thrombocytopathies or coagulation disorders.
- •o Symptomatic CHD (exercise ECG recommended if necessary)
- •o Severe refractory hypertension
- •o Non-adjustable COPD
- •o severe osteoporosis
- •o acute migraines, epilepsy, dizziness
- •Taking antidepressants (SSRIs) and other drugs that affect quality of life
- •Medical or psychological condition (psychomotor deficits) that does not allow the patient to take part in the study
- •unwillingness to pass on personal illness data within the framework of the protocol
研究者
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