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临床试验/NCT04421131
NCT04421131已完成不适用

mHealth-supported Telecolposcopy for Cervical Cancer Programs in Low-resource Settings: Evaluation (mIVAA)

Duke University1 个研究点 分布在 1 个国家目标入组 112 人开始时间: 2021年1月8日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
112
试验地点
1
主要终点
Percentage of Women Referred to a Follow up Screening Appointment With a Colposcopist Who Did Not Attend the Appointment

研究概览

简要总结

The central hypothesis is that use of mIVAA (mobile Inspección Visual con Ácido Acético - Spanish for Visual Inspection with Acetic Acid (VIA)) will increase the proportion of VIA positive women who complete follow-up clinical evaluation compared to VIA positive women in situations in which mIVAA was not used, thus potentially improving cervical cancer treatment and survival rates. The study will collect qualitative and quantitative data to examine the feasibility and preliminary impact of mIVAA on reducing attrition for follow-up clinical evaluations.

详细描述

The study will be conducted in Lima, Peru in the context of mobile units operated by La Liga for promoting cancer screening. mIVAA comprises two components: a digital imaging device and a telemedicine platform.

  1. The digital imaging device is either a mobile phone camera or the pocket colposcope plugged into a mobile phone.
  2. The telemedicine platform is mobile phone-based, with an interface for midwives in the mobile units to enter patient information and acquire and upload cervical images, and an interface for the colposcopists based remotely to review the cervical images and patient information and return feedback.

The specific aim is to pilot test mIVAA in a community-based setting in Peru.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Screening
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

  • Age 18 or older
  • Patients coming to the mobile unit for cervical cancer screening
  • Willing to allow use of mIVAA during screening with VIA.
  • Agree to be audio recorded

排除标准

  • Currently pregnant
  • History of hysterectomy
  • Does not understand the study purpose and details
  • Is not willing to sign an informed consent

结局指标

主要结局

Percentage of Women Referred to a Follow up Screening Appointment With a Colposcopist Who Did Not Attend the Appointment

时间窗: up to 142 days

次要结局

  • Number of Visual Inspection With Acetic Acid (VIA) Screened Women Who Are VIA+(up to 142 days)
  • Average Number of Days From Screening to When a Follow up Appointment is Scheduled(up to 142 days)
  • Number of Women Screened Positive (i.e., Suspicious) for Cervical Cancer/Pre-cancer by Expert Colposcopist(up to 142 days)
  • Median Number of Days From Screening to When a Follow up Appointment is Scheduled(up to 142 days)
  • Percentage of mIVAA Screened Women With Expert Feedback Within 0-7 Days of mIVAA Screening Date(up to 7 days)
  • Average Number of Attempts Per Woman Before a Readable Image is Obtained by Midwife(up to 142 days)
  • Percentage of Women Approached Who Refused to Participate in Study(up to 142 days)
  • Number of Women Screened Positive (i.e., Suspicious) for Cervical Cancer/Pre-cancer by Midwife(up to 142 days)
  • Number of Instances of Network Failure(up to 142 days)
  • Percentage of Women Approached Who Consented to Participate in Study(up to 142 days)
  • Percentage of Women Who Were Screened Using mIVAA(up to 142 days)
  • Average Number of Hours From Screening to When Expert Enters Feedback Using mIVAA(up to 142 days)
  • Percentage of mIVAA Screened Women With at Least 1 Image Rated as Readable by Expert(up to 142 days)

研究者

发起方
Duke University
申办方类型
Other
责任方
Sponsor

研究点 (1)

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