ISRCTN97662203进行中(未招募)Unknown
A phase II, randomised feasibility basket trial of a personalised, multi-component, home-based exercise programme on disease-free survival among early-stage high-risk recurring cancers in Yorkshire
niversity of Hull0 个研究点目标入组 660 人开始时间: 2024年1月15日最近更新:
适应症
试验速览
- 阶段
- Unknown
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 660
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Adults aged 18 or older
- •2. Diagnosed with early-stage high-risk cancer, defined as:
- •2.1. Non-small cell lung cancer: diagnosed with stages II or IIIA disease
- •2.2. Breast: Triple-negative breast cancer: diagnosed with = stage II (defined as an Allred score < = 4 and her2 negative),
- •2.3. Bowel: diagnosed with stage II, T4 disease only or any stage III disease
- •3. Within 12 weeks of completing primary treatment (e.g., surgery +/- chemo and/or radiation therapy) with curative intent, or for those on adjuvant immunotherapy or tyrosine kinase inhibitors, as soon as they begin this phase of their adjuvant treatment,
- •4. Willing and able to complete study measures and be randomised,
- •5. Able to provide informed consent,
- •6. Willing and able to engage remotely either by phone or video-based communications.
排除标准
- •1. Being treated for low-risk early-stage or incurable cancers,
- •2. Having an irreversible unstable acute condition (e.g. acute infection, severe uncontrolled symptoms) or underlying chronic condition or disease (e.g. severe arthritis or dementia) that would impact study compliance.
- •3. Mental capacity impaired to the extent that a course of systemic anti-cancer therapy is considered inappropriate by treating oncologist
研究者
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