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临床试验/NCT04068870
NCT04068870Unknown1 期

Modification of an Evidence-based Family Planning Intervention for a New Target Population: Postpartum Women in Nakaseke District, Uganda - Pilot Phase, Two Arm

University of Vermont1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2019年8月5日最近更新:
适应症
干预措施

试验速览

阶段
1 期
入组人数
20
试验地点
1
主要终点
Period prevalence use of a prescription contraceptive

研究概览

简要总结

The purpose of this study is to test whether offering incentives to encourage women to attend one-on-one family planning education sessions and offering free, onsite prescription contraceptive methods increases use and continuation of prescription contraception among postpartum women in Uganda. This intervention is modified from one that has been effective outside of Uganda.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • 18-45 years of age
  • Not planning on getting pregnant in the next 4 months
  • Less than 3 months postpartum
  • No history of tubal ligation or hysterectomy
  • No recent prescription contraceptive use (no pill, intrauterine device or implant use in the past 7 days or injection use in the past 3 months)
  • Medically eligible to use prescription contraceptives
  • Bringing baby to immunization clinic for the first time

排除标准

  • Failure to meet the aforementioned inclusion criteria

研究组 & 干预措施

Contraceptive management program

Experimental

干预措施: Contraceptive management program (Behavioral)

Usual care

No Intervention

结局指标

主要结局

Period prevalence use of a prescription contraceptive

时间窗: 6 months after delivery

Period prevalence use of a prescription contraceptive

次要结局

未报告次要终点

研究者

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

Sarah Heil

Professor

University of Vermont

研究点 (1)

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