跳至主要内容
临床试验/NCT05025891
NCT05025891Unknown不适用

Reducing Inequalities in Access to Care in French Guiana: ISe-santé, a Randomized Study Evaluating a Model for Implementing E-health in the Management of HIV

Centre Hospitalier de Cayenne2 个研究点 分布在 1 个国家目标入组 450 人开始时间: 2021年2月4日最近更新:
适应症

试验速览

阶段
不适用
入组人数
450
试验地点
2
主要终点
Comparison of the proportions of patients who followed the schedule proposed by the physician at inclusion (or revised during important events) in the 3 arms.

研究概览

简要总结

It is a randomized, controlled, open-label, parallel group study of 3 arms, among patients followed for chronic HIV infection at Cayenne hospital. The main objective of the study is to evaluate the effectiveness of follow-up of these patients by teleconsultation associated or not with health mediation.

详细描述

The COVID-19 pandemic crisis has strained health systems, and chronic disease monitoring has often been put on hold, without yet really measuring the resulting health impact. In this context, e-Health has benefited from considerable momentum to overcome the shortcomings that have arisen, to allow remote monitoring of patients infected with COVID 19, to protect patients and caregivers and avoid nosocomial infections. Telemedicine is all the more relevant in Guyana as there are issues of geographic isolation, lack of specialists and critical mass of health professionals. In French Guiana, faced with the arrival of teleconsultation tools, a fear of professionals is their applicability for the most vulnerable populations, not knowing how to read or speak French and having restricted access to digital technology. Moreover HIV infection is an ever stigmatizing infection affecting populations that are often extremely precarious, requiring specialist monitoring and lifelong treatment.

The study team propose to carry out a randomized, controlled, open-label, parallel group study of 3 arms, among patients followed for chronic HIV infection at Cayenne hospital : 1/ Control group with classic follow-up at Cayenne hospital. 2/Teleconsultation only group: patients referred to the remote monitoring platform without specific support. 3/Teleconsulation group + mediator: patients referred to the remote monitoring platform with support from a health mediator Patients will be followed every 3 months or 6 months depending on the judgment of the investigating physician for 12 months in the study (primary endpoint evaluated at 1 year). Number of patients to be included: 450 patients.

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
Double (Participant, Outcomes Assessor)

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

  • Patients with chronic HIV infection.
  • Patient with a regular follow-up for more than three months in the adult day hospital or in the infectious diseases department of the Cayenne Hospital Center.
  • Patient of legal age.
  • Patient having signed the consent form..

排除标准

  • Pregnant patient
  • Patient with a severe neurological or psychiatric history (significant cognitive disorders, intellectual disability).
  • Patient with a physical disability that prevents communication via the e-Health platform (mute patient, visually and hearing impaired, specific manual motor disability, bedridden patient).
  • Patient who does not master one of the languages available at the mediation.
  • Patients under guardianship or trusteeship, people under protective measures

结局指标

主要结局

Comparison of the proportions of patients who followed the schedule proposed by the physician at inclusion (or revised during important events) in the 3 arms.

时间窗: The inclusion period (1 year)

次要结局

  • Patient satisfaction score assessed with study specific questionnaire(The inclusion period (1 year))
  • Evaluation of the material needs for the implementation and maintenance of the e-health platform(The inclusion period (1 year))
  • Measurement of the average intervention time of the ETP nurse per patient(The inclusion period (1 year))
  • Compare the patients followed up with the platform and the patients followed up in classic consultation on: the proportion of check-ups done during the same duration of follow-up, the proportion of patients with an undetectable viral load, the proportion(The inclusion period (1 year))
  • proportion of check-ups done during the same duration of follow-up between patients followed up with the platform and the patients followed up in classic consultation(The inclusion period (1 year))
  • Identification of the best strategy for implementing an e-Health platform in French Guiana in the management of chronic HIV infection(The inclusion period (1 year))
  • Evaluation of the material needs to guarantee accessibility of the consultation places(The inclusion period (1 year))
  • proportion of patients with an undetectable viral load between patients followed up with the platform and the patients followed up in classic consultation(The inclusion period (1 year))
  • The proportion of patients throughout the inclusion period (1 year) likely to use the platform will be assessed using the number of patients meeting the inclusion criteria (having agreed to participate in the research or not).(The inclusion period (1 year))
  • The obstacles to the use of an e-health platform will be evaluated using a questionnaire for caregivers and patients and based on the number of failed connections(The inclusion period (1 year))
  • Caregiver satisfaction score assessed with study specific questionnaire(The inclusion period (1 year))
  • Measurement of the average intervention time of the doctors per patient(The inclusion period (1 year))
  • Measurement of the average intervention time of the mediators per patient(The inclusion period (1 year))
  • Questionnaire for all the care providers assessed with study specific questionnaire(The inclusion period (1 year))

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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