跳至主要内容
临床试验/NCT01990001
NCT01990001已完成不适用

Randomized Trial of Provider-Assisted Versus Patient-Initiated Enrollment in the Bedsider.Org Online Contraceptive Reminder Tool

Medical University of South Carolina2 个研究点 分布在 1 个国家目标入组 118 人开始时间: 2012年8月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
118
试验地点
2
主要终点
Proportion of patients using the online reminder tool three months after enrollment

研究概览

简要总结

The broad objective of this research is to determine whether a quick, simple intervention will increase utilization of contraceptive reminders and adherence to short-term contraceptive regimens. Such an intervention could be implemented easily with no additional resources into a busy clinical practice.

详细描述

The specific aims of the study are to:

  1. Measure the difference in reminder utilization over three months between patients who are assisted with initiating the reminder system during their office visit versus those who are encouraged to self-initiate after the visit.
  2. Assess whether provider-assisted enrollment in the online reminder system improves adherence to a short-term contraceptive regimen compared to self- initiated enrollment after the visit.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
盲法
None

入排标准

年龄范围
18 Years 至 29 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Female, 18-29 years old
  • Prescribed one of the following birth control:
  • Oral contraceptive pills, vaginal ring, transdermal patch, or Depo Provera
  • Able to provide consent
  • Have regular access to a computer, Ipad, or a hand-held device such as a smartphone.
  • Women must be able to read and speak English(Bedsider website in not translated into Spanish)

排除标准

  • Over the age of 30 years old
  • Non-English Speaking
  • Limited or no access to computer, Ipad or hand-held device(smartphone)

研究组 & 干预措施

Office enrollment in the online contraceptive reminder system

Experimental

Members of this arm were enrolled in the reminder system during their visit.

干预措施: enrollment in online reminder system (Other)

Control

No Intervention

Members in the control group were not enrolled in the reminder system

结局指标

主要结局

Proportion of patients using the online reminder tool three months after enrollment

时间窗: 3 months

Measure the difference in reminder utilization over three months between patients who are assisted with initiating the reminder system during their office visit versus those who are encouraged to self-initiate after the visit. The primary outcome, which is proportion of reminder users, will be assessed three months after enrollment

次要结局

  • Assess whether provider-assisted enrollment in the online reminder system improves adherence to a short-term contraceptive regimen compared to self- initiated enrollment after the visit.(3 months)

研究者

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

Ashlyn H. Savage, MD

Assistant Professor of Obstetrics and Gynecology

Medical University of South Carolina

研究点 (2)

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