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临床试验/NCT05067049
NCT05067049Unknown不适用

Evaluation of the Impact of a Connected Application on the Follow-up of Patients Treated for Glial Lesions Operated: a Prospective, Randomized Study

Ramsay Générale de Santé2 个研究点 分布在 1 个国家目标入组 66 人开始时间: 2019年2月1日最近更新:
适应症

试验速览

阶段
不适用
入组人数
66
试验地点
2
主要终点
Assessment of the impact of the connected mobile monitoring application on the quality of life, at 6 months, of patients treated for an operated glioma.

研究概览

简要总结

This study is to evaluate the efficacy of a mobile app for monitoring the quality of life of patients but also on detection delay of side effects and/or complications linked to the therapeutic management. This allow to adapt their care more quickly, through a prospective randomized study. The impact of this connected monitoring of patients' anxiety will also be evaluated in this study as well as the time taken by the medical team to manage alerts generated by this application.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
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

  • Male or female over 18 years old without upper age limit.
  • Subject operated for a non-recurrent glioma (grade II or III or IV glioma / glioblastoma) according to the WHO classification 2016;
  • Subject with a connected support (smartphone,...) to download the connected tracking application.
  • Unprotected adult within the meaning of the law
  • Subject affiliated to a health insurance scheme
  • Subject having signed an informed written consent

排除标准

  • Minor subject, pregnant or breastfeeding woman;
  • Subject under a measure of legal protection, guardianship or deprived of liberty by judicial or administrative decision;
  • Antipsychotic treatment (neuroleptic or lithium)
  • Subjects with documented cognitive disorders (Alzheimer, other dementia)
  • Subject with a personal medical history of psychiatry
  • Subject unable to complete a questionnaire on his own (inability to read French language , severe cognitive disorders)
  • Medical contraindication to performing an MRI (pace-maker) or scanner;
  • Subject refusing to sign informed consent.

结局指标

主要结局

Assessment of the impact of the connected mobile monitoring application on the quality of life, at 6 months, of patients treated for an operated glioma.

时间窗: 6 months

The primary outcome measure is the difference in quality of life assessed by the QLQ-BN20 scale at 6 months, compared to inclusion. This scale is made up of 20 items which are grouped into 4 dimensions (future uncertainty, visual disorder, motor dysfunction, and communication deficit) and 7 isolated items.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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