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临床试验/NCT04980989
NCT04980989已完成不适用

A Prospective Randomized Trial of Interactive Telemonitoring in the Follow-up of Patients Treated for Breast Cancer

Helsinki University Central Hospital0 个研究点目标入组 765 人开始时间: 2015年6月15日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
765
主要终点
Patient preference for follow-up modality

研究概览

简要总结

Patients with early breast cancer were randomized at the final visit of adjuvant radiotherapy to surveillance by phone calls or by mobile Noona software. After six months the groups were crossed over to the other arm. At 12 months the patients were asked their preference which was the primary end-point. At baseline, 6 months and 12 months the patients answered the other questionnaires.

详细描述

Patients with early breast cancer were randomized at the final visit of adjuvant radiotherapy to surveillance by phone calls or by mobile Noona software. After six months the groups were crossed over to the other arm.

The primary end point was to find out patient preference for the modality of surveillance. Secondary endpoints were patient satisfaction, symptoms, quality of life and cost of follow-up during surveillance modalities.

At 12 months the patients were asked their preference for the follow-up modality of early breast cancer. At baseline, 6 months and 12 months the patients answered the other questionnaires on quality of life, symptoms, patient satisfaction and use of other health-care services. Information on the cost of follow-up was gathered from the hospital and other registries.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Health Services Research
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

  • Adult patients with early breast cancer after primary treatment including also radiotherapy (the patients were randomized at the final visit of radiotherapy)

排除标准

  • not able to use a computer
  • another malignancy

结局指标

主要结局

Patient preference for follow-up modality

时间窗: At 12 months during follow-up of early breast cancer

Questionnaire of patient preference

次要结局

  • Quality of life during follow-up modality(At baseline, 6 months and 12 months)
  • Patient satisfaction(At 6 months and 12 months)
  • Symptoms(At baseline, 6 months and 12 months)
  • Use of other healthcare services(At 6 months and 12 months)

研究者

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

Johanna Mattson

Physician-in-Chief

Helsinki University Central Hospital

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