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临床试验/NCT02380781
NCT02380781已完成不适用

Contraceptive Counseling in the Postpartum Period

University Hospitals Cleveland Medical Center2 个研究点 分布在 1 个国家目标入组 179 人开始时间: 2015年3月1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
179
试验地点
2
主要终点
Choice of contraceptive method

研究概览

简要总结

This is a prospective randomized control trial in which we propose an intervention in the immediate post-partum period to educate women about contraceptive options, particularly long acting reversible contraception (LARC) methods with an aim of increasing the amount of women who choose a LARC method.

详细描述

Eligible participants will be identified in the post-partum period and will be randomized to one of two groups. The control group will receive the standard of care contraceptive counseling which includes any prenatal counseling they received as well as information from the nurse practitioner that rounds on them in the post-partum period. The intervention group will also receive the standard of care contraceptive counseling but will also watch a 10 minute video created by the CHOICE project which counsels on different contraceptive options. Both groups will fill out a pre-intervention questionnaire as well as a post-intervention questionnaire 24hrs later. The primary outcome will be which type of contraception each woman chooses. The secondary outcomes will include determining if the women come to their post-partum visits as well as if they get the method of contraception they chose on the post-partum floor.

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 (Participant)

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 giving birth at University Hospitals Case Medical Center
  • Patient of the Women's Health Center
  • Women delivering only one child
  • Women receiving contraceptive counseling from the nurse practitioner that cares for the postpartum unit

排除标准

  • Severe neonatal complication at time of delivery (neonatal death, neonatal admission to the neonatal intensive care unit (NICU) except in cases of chorioamnionitis)
  • Severe maternal complication at time of delivery (patient requiring intensive care unit care, patient requiring hysterectomy at time of delivery)
  • Preterm delivery <34 weeks

结局指标

主要结局

Choice of contraceptive method

时间窗: 24 hours post-intervention

Will be obtained through use of a questionnaire.

次要结局

  • Obtained desired method of contraception(12 weeks post-intervention)
  • Return to clinic for postpartum visit(12 weeks post-intervention)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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