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临床试验/NCT04437719
NCT04437719已完成不适用

Longitudinal Prospective Cohort Study to Describe the Clinical Characteristics of COVID-19, the Acquired Immune Response and the Biological and Clinical Parameters of Patients Followed in Oncology by the Saint-Joseph Hospital Group, Paris, France for a Period of 6 Months During the COVID-19 Pandemic in 2020

Fondation Hôpital Saint-Joseph2 个研究点 分布在 1 个国家目标入组 34 人开始时间: 2020年6月29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
34
试验地点
2
主要终点
COVID-19 infection's symptoms

研究概览

简要总结

This registry will allow to evaluate the correlation of the incidence and evolution of associated symptoms of infection of COVID-19 with the biological and clinical parameters in patients followed in Oncology during the COVID-19 pandemic.

详细描述

Prior to conducting any of the screening tests, the Investigator or his designee will explain the trial fully to the prospective patient and provide him with a copy of the Patient Information Leaflet/Informed Consent Form.

If the patient is willing to participate to the trial, his given oral, free, informed and express consent will be collected and traced in his medical file.

The screening questionnaire will be completed. The patient's suitability for the trial will be confirmed by the inclusion/exclusion criteria .

Following completion of the Baseline Questionnaire, patients will receive the Daily Questionnaire. This is designed to assess if they have developed symptoms associated with COVID-19 infection.

If a participant responds that they are not feeling well, a series of follow-up questions will be asked regarding what symptoms they are currently experiencing.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
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

  • Patient over 18 years of age
  • Patient followed in the medical oncology department of Paris Saint-Joseph Hospital Paris in France
  • Patient Having regular access to smartphone and internet sufficient to support study demands
  • French-speaking patient
  • Affiliation to the social security network
  • Willing and able to provide given oral, free, informed and express consent

排除标准

  • Patients unable or unwilling to perform all requested study tasks
  • Patient under tutorship or curatorship
  • Patient deprived of liberty
  • Pregnant or lactating patient

结局指标

主要结局

COVID-19 infection's symptoms

时间窗: Observational period of 6 months

Evaluation of the proportion of patients with COVID-19 infection's symptoms known to be associated with COVID-19 diagnosis (fever, cough, loss of taste and smell, sore throat, muscle pain, diarrhea, fatigue, difficulty eating and drinking and shortness of breath) followed during a period of 6 months.

次要结局

  • Incidence and course of symptoms of COVID-19 infection(During a period of 6 months)
  • Correlation of the COVID-19 infection with the biological and clinical data of patients(After a period of 6 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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