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临床试验/NCT04913714
NCT04913714已完成不适用

10+10+30 Infant Vaccines Communication Via Radio in Ethiopia

Syracuse University3 个研究点 分布在 2 个国家目标入组 1,320 人开始时间: 2020年10月13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
1,320
试验地点
3
主要终点
Penta 3 vaccine coverage of infant

研究概览

简要总结

A cohort study to investigate the effectiveness of radio intervention comprising 10-minute of drama, 10-minute of discussion led by community extension workers, and 30-minute phone-in from listeners on childhood vaccination coverage and timeliness

详细描述

The evaluation is conducted in 2 districts located in the Oromia region of Ethiopia. One of the districts will be allocated to receive the 3-month radio intervention while the other district that will not have access to the radio intervention will serve as the control.

Data collection includes survey of mothers at two "key" times: at baseline (when infants are at most 5 weeks old; but before beginning the intervention) and at endline (including examination of infant vaccination records) at most 21 days after the end of the radio intervention. The same mothers and infants to be followed at endline.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Other
盲法
Single (Outcomes Assessor)

盲法说明

Data analyst did not know which group received the intervention

入排标准

年龄范围
1 Day 至 5 Weeks(Child)
性别
All
接受健康志愿者

入选标准

  • Mother, with infant of at most 5 weeks old; Lives in the study district; Consents to participate in study

排除标准

  • Mother, with infant of more than 5 weeks old; Does not live in study district; Does not consent to participate in study

结局指标

主要结局

Penta 3 vaccine coverage of infant

时间窗: up to 3 weeks after the intervention ends

Infant's vaccination record or mother's recall based on interviewer-administered questionnaire

次要结局

  • Perceived barriers to vaccination(Immediately before intervention starts, and up to 3 weeks after the intervention ends)
  • Full coverage of infant vaccines(up to 3 weeks after the intervention ends)
  • Cues to action(Immediately before intervention starts, and up to 3 weeks after the intervention ends)
  • Timeliness of infant vaccines(up to 3 weeks after the intervention ends)
  • Perceived benefits of infant vaccines(Immediately before intervention starts, and up to 3 weeks after the intervention ends)
  • Perceived susceptibility to vaccine-preventable diseases in children(Immediately before intervention starts, and up to 3 weeks after the intervention ends)
  • Perceived severity of vaccine-preventable diseases in children(Immediately before intervention starts, and up to 3 weeks after the intervention ends)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (3)

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