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临床试验/NCT05803538
NCT05803538尚未招募不适用

Participant Centered Active Surveillance for Adverse Event Following Measles Immunization in Gedeo Zone, Ethiopia, 2022. A Multi-center Open-label Randomized Control Trial

Dilla University2 个研究点 分布在 1 个国家目标入组 391 人开始时间: 2023年5月15日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
391
试验地点
2
主要终点
Response rate

研究概览

简要总结

Introduction Participant centered active adverse event following immunization (AEFI) surveillance can offer real time vaccine safety data and help in signal detection. Evidence showed that it is still difficult to get AEFI from passive reporting in Ethiopia. Vast novel method of enhanced AEFI surveillance has been practiced globally. However, those methods had serious limitations including the requirement of high resource and expertise. Hence, there is a need to find the most flexible low cost and integrated AEFI surveillance system. To the best of our knowledge, there has no published research in Ethiopia which compare Participant diary, SMS, and telephone interview for the purpose of active AEFI surveillance.

Objective: To assess participant centered active adverse event surveillance following measles immunization at Gedeo Zone health facilities, Ethiopia.

Method: An open randomized trial will be employed from October 1, 2022- December 1, 2023, at Gedio Zone health facilities. All parents, care givers/guardians whose child receive vaccine during the study period in the study site will be included in the study. A total of 391participants will be randomized to SMS, telephone interview or diary card group using random number generator on Excel. Every participant will be contacted on day seven to request them whether they experience any AEFI. Differences in proportions will compared using chi-square tests. A 0.05 level of significance will be used for all analyses. Independent sample t-tests will be used to compare the mean time (in days) required to collect complete AEFI data by SMS, telephone interview and diary card. Multinominal logistic regression analyses will be used assess the factors associated with effective use of tailored SMS, telephone interview and diary card for the AEFI active surveillance. To further investigate the association between the vaccine and the adverse events and factors associated with vaccine binary and multi variable logistic regression will be used.

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
Single (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

  • Parents, care givers/guardians, whose child receive vaccine.
  • ≥18 years of age.
  • Willing to adhere to study procedures, which will include a randomization.
  • Willing to participate

排除标准

  • Unable to give informed consent because of cognitive impairment.
  • Those who are both illiterate and don't have mobile phone.

结局指标

主要结局

Response rate

时间窗: 7 days

To compare response rate of tailored SMS, telephone interview and diary card for the AEFI active surveillance

次要结局

  • AEFI's reported from each group and feasibility of participant centered AEFI active surveillance(7days)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Dawit Getachew Getachew

Mr.

Dilla University

研究点 (2)

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