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临床试验/NCT04506476
NCT04506476招募中不适用

Randomisierte Studie Zum Nutzen Des Fitnesstracker Basierten Aktivitätstrainings während Einer Adjuvanten Bestrahlung Des Mammakarzinoms (OnkoFit I)

University Hospital Tuebingen2 个研究点 分布在 1 个国家目标入组 201 人开始时间: 2020年8月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
201
试验地点
2
主要终点
Evaluation of the impact of an activity tracker based fitness programme on the fatigue syndrome

研究概览

简要总结

This randomized three-arm trial will test the benefit in terms of cancer related fatigue of an activity tracker based exercise training during adjuvant radiotherapy in breast cancer patients.

详细描述

This monocentric, three-arm, randomized, controlled clinical trial evaluates the effect of an activity tracker based exercise program in breast cancer patients on the fatigue syndrome during adjuvant radiotherapy. Quality of Life and the intensity of fatigue will be documented with the fatigue subscale of the FACIT Questionnaire three months after adjuvant radiotherapy.

研究设计

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

入排标准

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

入选标准

  • Capacity for consent
  • Minimum age 18
  • Presence of breast cancer
  • Indication for adjuvant radiotherapy of breast cancer after breast-conserving surgery or Ablatio mammae

排除标准

  • Participation in any other interventional study
  • Pregnancy
  • Contraindication against physical activity/sport and others
  • Severe cardiovascular pre-existing conditions (after myocardial infarction, apoplexy in the last 6 months, congestive heart failure NYHA > I°)
  • preexisting diseases with are relevantly accompanied by a limited mobility in patients (e.g. paraparesis of the lower limbs)
  • ECOG Status 3-4
  • prior use of activity trackers

结局指标

主要结局

Evaluation of the impact of an activity tracker based fitness programme on the fatigue syndrome

时间窗: 3 Months after completion of adjuvant radiotherapy of breast cancer

This endpoint will be evaluated by the FACIT-F (Functional Assessment of Chronic Illness Therapy-Fatigue) subscale of the FACIT questionnaire (Physical well-being values 0-28, 28 worse outcome; social/family well-being values 0-28, 28 better outcome; emotional well-being values 0-24, 24 worse outcome; functional well being values 0-28, 28 better outcome; additional factors values 0-64, 64 worse outcome

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr. Cihan Gani

Senior Physician

University Hospital Tuebingen

研究点 (2)

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