跳至主要内容
临床试验/NCT06790069
NCT06790069已完成不适用

Safety and Feasibility of the Integration of Ada Into the Mobile MomConnect Information Service for Pregnant Women and New Mothers in South Africa

Ada Health GmbH1 个研究点 分布在 1 个国家目标入组 968 人开始时间: 2023年5月4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
968
试验地点
1
主要终点
Proportion of appropriate advice by the SC for mother and child

研究概览

简要总结

The goal of this study is to evaluate the integration of a symptom checker (SC) into the MomConnect (MC) platform to support maternal healthcare in South Africa. The main questions it aims to answer are:

  • Does the SC provide safe and appropriate medical advice?
  • Does the SC help mothers make informed decisions about when and where to seek healthcare, saving time and money by avoiding unnecessary visits?
  • Does the SC improve access to care for those facing significant healthcare barriers?

Participants will answer survey questions before and after using the SC. A subset of participants will also be invited to participate in structured telephone interviews.

The study will help researchers assess the SC's impact on healthcare decisions and resource use in South Africa.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Other

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者
否

入选标准

  • •Women registered with MomConnect, who would like to assess their or their child's symptoms
  • •At least 18 years of age
  • •Women with access to WhatsApp
  • •Capable of completing a symptom assessment in English

排除标准

  • •Incapable of completing a symptom assessment in English via WhatsApp (e.g. due to illiteracy, language barrier, mental impairment or inebriation or other incapacity or lack of access to WhatsApp)

结局指标

主要结局

Proportion of appropriate advice by the SC for mother and child

时间窗: From data collection with participant enrolment to the completion of panel ratings, approximately 2-3 months after participant enrolment.

Proportion of safe advice by the SC for mother and child

时间窗: From data collection with participant enrolment to the completion of panel ratings, approximately 2-3 months after participant enrolment.

次要结局

  • Potential prevention of a health problem in Perinatal Period for Mother or Child(From data collection with participant enrolment to the completion of panel ratings, approximately 2-3 months after participant enrolment.)
  • Potential prevention of a SEVERE health problem in Perinatal Period for Mother or Child(From data collection with participant enrolment to the completion of panel ratings, approximately 2-3 months after participant enrolment.)
  • Potential Occurrence of a health problem (adverse event) in Perinatal Period for Mother and Child(From data collection with participant enrolment to the completion of panel ratings, approximately 2-3 months after participant enrolment.)
  • Potential Occurrence of a SEVERE health problem (severe adverse event) in Perinatal Period for Mother or Child(From data collection with participant enrolment to the completion of panel ratings, approximately 2-3 months after participant enrolment.)
  • Health seeking behaviour before and after using Ada+MomConnect(From data collection with participant enrolment to the completion of the follow-up survey send out 1 week after enrolment.)
  • Number of participants who consulted an HCP after using Ada+MomConnect(After completion of the follow-up survey send out 1 week after enrolment.)
  • Gaining of health information in a fast and standardised way(On the day of enrolment.)
  • Usability(On the day of enrolment.)
  • Time saved from avoiding unnecessary healthcare consultations(On the day of enrolment.)
  • Time saved and associated estimate of income retained through avoiding unnecessary healthcare consultations(On the day of enrolment.)
  • Healthcare resource utilisation(On the day of enrolment.)
  • Direct Healthcare costs(On the day of enrolment.)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验