跳至主要内容
临床试验/ISRCTN97662203
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

发起方
niversity of Hull

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CANFit: A personalised home-based exercise programme... | 临床试验