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临床试验/NCT03956030
NCT03956030终止不适用

Effect of Formal Contraception Handouts on Postpartum Birth Control Use and Methods

Milton S. Hershey Medical Center2 个研究点 分布在 1 个国家目标入组 8 人开始时间: 2020年9月10日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
8
试验地点
2
主要终点
Contraception Use

研究概览

简要总结

The hypothesis of this study is to determine if distribution of a standardized educational handout on contraceptive options given to patients in the prenatal office setting will increase contraception use six months postpartum.

详细描述

Reducing unintended pregnancies and those that are conceived within 18 months of a previous livebirth is an important health concern in the United States. Both unintended and close-interval pregnancies constitute 40% and 35% of pregnancies in the United States respectively with some overlap between the two categories and are associated with adverse maternal and fetal outcomes. A national survey found that 17.8% of women using 'less-effective' methods and 23% of women using no birth control became pregnant in ≤18 months2. Access to better contraception education could potentially decrease the proportion of unintended pregnancies and close-interval pregnancies. In addition to the health concerns, 58% of women in the US would like more information about contraceptive options, and organized handouts on birth control have been shown to contribute to the choice in birth control. However, there has been conflicting evidence about which educational methods increase postpartum contraception use. Therefore, the investigators propose a randomized controlled trial (RCT) that assesses whether a handout on contraception options increases postpartum birth control use. The control group would receive a nutrition handout, and the intervention group would receive a handout on birth control options in addition to each receiving the standard of care. The researchers would also give pre- and post-natal questionnaires, covering patient satisfaction, intention to use birth control, and how often a provider discusses birth control options.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • Women who are pregnant and are 24-28 weeks gestational age at the time of recruitment
  • Women >18 years of age
  • Women with low-risk pregnancies

排除标准

  • Women who receive prenatal care by the Maternal Fetal Medicine department for high-risk pregnancies
  • Women who are members of an at-risk population including any women who is a prisoner, cannot provide consent, or is <18 years of age
  • Non-English speaking

结局指标

主要结局

Contraception Use

时间窗: 8 weeks postpartum

Participants were sent a survey electronically at 8 weeks which asked the question "Now that you have delivered, are you currently using birth control? (yes or no)" The data table reflects the number who answered YES and the number who answered NO to this question per group.

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

Christina DeAngelis

Assistant Professor Women's Health Division

Milton S. Hershey Medical Center

研究点 (2)

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