Home or Office Visit for Insertion of Etonogestrel Implant: A Pilot Study
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 40
- 试验地点
- 2
- 主要终点
- Insertion rates of implantable birth control
研究概览
简要总结
This is a pilot study in which women who desire an etonogestrel implant will be randomized to either a home or office insertion visit. The purpose of this research is to study the interest in, feasibility of, and rates of insertion for implantable birth control (Implanon®/Nexplanon®) when inserted at home visit appointments compared to standard office visit appointments.
The ultimate goal of the study is to reduce barriers to insertion of the etonogestrel implant and increase consistent and correct contraception use by introducing a previously unexplored method of access, the home visit.
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 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- 未提供
排除标准
- 未提供
结局指标
主要结局
Insertion rates of implantable birth control
时间窗: Two weeks post-implant insertion at the follow-up telephone call
Assess rates of insertion of etonogestrel contraceptive implant in women randomly assigned to home visits or standard office visits.
次要结局
- Interest in home visit option(Within 6-8 weeks of enrollment)
- Rates of return for postpartum follow-up(Within 6-8 weeks of enrollment)
研究者
Suji Uhm
MD/MPH Student
Case Western Reserve University