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临床试验/NCT03774797
NCT03774797已完成不适用

Immediate Postpartum LARC Implementation: Pilot Study at Michigan Medicine

University of Michigan1 个研究点 分布在 1 个国家目标入组 592 人开始时间: 2018年9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
592
试验地点
1
主要终点
Patient experience of care

研究概览

简要总结

The objective of this study is to test and disseminate tools that drive successful immediate postpartum Long-Acting Reversible Contraception (LARC) implementation. The long-term goal is to reduce unintended pregnancy soon after childbirth by increasing access to immediate postpartum LARC for women who desire it.

详细描述

Based on previous work, the investigators have generated a toolkit to guide the integration of immediate postpartum LARC services into widespread clinical practice. In the proposed work, this toolkit will be used to initiate immediate postpartum LARC services in a single site with low baseline immediate postpartum LARC uptake (Michigan Medicine). The investigators will conduct a feasibility study using mixed methods to assess acceptability and appropriateness of toolkit items; patient experience of care; immediate postpartum LARC utilization rate; and prenatal contraceptive counseling rate.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Cross Sectional

入排标准

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

入选标准

  • •Female (patients)
  • •Pregnant (patients)
  • •Receiving obstetrical care at Michigan Medicine (patients)
  • •L&D provider at Michigan Medicine (providers)

排除标准

  • •non-English speaking
  • •unable to provide informed consent

结局指标

主要结局

Patient experience of care

时间窗: Surveys will be collected from pregnant or postpartum women, during the 6-12 months after implementation of a new protocol for peripartum contraceptive care

Patient online surveys about their experience of care during prenatal visits, hospital stay, or postpartum office visit

Acceptability of implementation process - study site maternity care providers

时间窗: Surveys will be collected during the 6-12 months after implementation of a new protocol for peripartum contraceptive care

Online survey assessing overall experience of care delivery, acceptability and appropriateness of implementation tools

Appropriateness of implementation process - study site maternity care providers

时间窗: Surveys will be collected during the 6-12 months after implementation of a new protocol for peripartum contraceptive care

Online survey assessing overall experience of care delivery, acceptability and appropriateness of implementation tools

Appropriateness of care process - patients

时间窗: Surveys will be collected from pregnant or postpartum women, during the 6-12 months after implementation of a new protocol for peripartum contraceptive care

Online survey assessing experience of care, acceptability and appropriateness of implementation tools

Acceptability of care process - patients

时间窗: Surveys will be collected from pregnant or postpartum women, during the 6-12 months after implementation of a new protocol for peripartum contraceptive care

Online survey assessing experience of care, acceptability and appropriateness of implementation tools

次要结局

  • Appropriateness of implementation toolkit items - patients(Interviews will take place after the survey is completed, during the 6-18 months after implementation of a new protocol for peripartum contraceptive care)
  • Acceptability of implementation toolkit items - providers(Interviews will take place after the survey is completed, during the 6-18 months after implementation of a new protocol for peripartum contraceptive care)
  • Acceptability of implementation toolkit items - patients(Interviews will take place after the survey is completed, during the 6-18 months after implementation of a new protocol for peripartum contraceptive care)
  • Appropriateness of implementation toolkit items - providers(Interviews will take place after the survey is completed, during the 6-18 months after implementation of a new protocol for peripartum contraceptive care)
  • Perinatal contraceptive counseling rate(Measured monthly, up to 24 months after toolkit implementation)
  • Immediate postpartum LARC provision rate(Measured monthly, up to 24 months after toolkit implementation)

研究者

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

Michelle H. Moniz

Assistant Professor

University of Michigan

研究点 (1)

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