跳至主要内容
临床试验/ACTRN12618001537246
ACTRN12618001537246已完成未知

Training midwives in the insertion of contraceptive implants to increase uptake in the immediate postpartum period: a feasibility pilot study

Family Planning NSW0 个研究点目标入组 34 人开始时间: 2018年9月13日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
34

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Non-randomised trial
主要目的
Educational / counselling / training

入排标准

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • Midwives are the primary participants for this study. Any Registered Midwife practicing in RPAH or Canterbury Hospital postnatal wards, birth centres or and Midwifery Group Practice that has an ongoing minimum workload of one shift per week will be eligible to participate.

排除标准

  • Midwives who do not have regular shifts at the participating hospitals or whose supervisors do not support their participation in the Implanon® NXT insertion training program.

研究者

相似试验