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临床试验/NCT03610854
NCT03610854Unknown不适用

Pilot Study for the Continuous Assessment of Biological Parameters Using a Fitness Tracker Before, During and After Radiochemotherapy or Chemotherapy in Patients With Oncological Diseases

University Hospital Tuebingen1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2018年4月18日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
50
试验地点
1
主要终点
Compliance for wearing the fitness tracker

研究概览

简要总结

The overall goal of the present trial is to evaluate the patients' compliance for wearing a commercially available fitness tracker during and after oncological treatments.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
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
All
接受健康志愿者

入选标准

  • Histologically confirmed malignant disease
  • Upcoming chemotherapy of radiochemotherapy
  • Eastern Co-operative Oncology Group (ECOG) performance score 0-2

排除标准

  • Pre-existing comorbidities that impair patient mobility.
  • Eastern Co-operative Oncology Group (ECOG) performance score 3-4

研究组 & 干预措施

Fitness tracker Arm

Experimental

Patients will be wearing a commercially available fitness tracker during radiotherapy or chemotherapy and four weeks after the end of treatment.

干预措施: Fitness Tracker (Device)

结局指标

主要结局

Compliance for wearing the fitness tracker

时间窗: Four weeks after the end of radiotherapy

Based on the read outs from the fitness trackers we will calculate the percentage of the days on which the tracker was worn, which is defined as the compliance.

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

Dr. Cihan Gani, Clinician Scientist

University Hospital Tuebingen

研究点 (1)

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